Health And Family Welfare Department has published Supply Of Surgical Items - Total Item 1 To 4441 (Part 8 :- Item No 2451 To 2800)- Collagen Wound Dressing Consists Of Collagen, Having A Porous Structure With Highly Pronounced Capillary Activity, Enabling It To Absorb Fluid, With The Continuous Absorptio. Submission Date for this Tender is 17-08-2023. Surgical Disposable Tenders in Vadodara Gujarat. Bidders can get complete Tender details and download the document.
Sr No | CorrigendumDate | Corrignedum | CorrigendumType | NewSubmissionDate |
1 | 29-Jul-2023 | 17-08-2023 |
Sl. No. | Item Title | Specification |
1 | Collagen Wound Dressing consists of collagen, having a porous structure with highly pronounced capillary activity, enabling it to absorb fluid, with the continuous absorption of exudate results in the intake of cell debris as well as inflammation inducing proteases and cytokines. 6X8X0.8 cm, | As per column no.2 |
2 | Collagen Wound Dressing consists of collagen, having a porous structure with highly pronounced capillary activity, enabling it to absorb fluid, with the continuous absorption of exudate results in the intake of cell debris as well as inflammation inducing proteases and cytokines. 8X12X0.8 cm | As per column no.2 |
3 | Activated Charcoal with Silver is an antimicrobial, flexible, soft, non-adherent rope which contains an activated charcoal fabric impregnated with silver in a non-woven cover that does not stick to the wound. The device is ideal for packing into deep and tunnel wounds and for use like a wound cover on superficial wounds. 10X10 cm, | As per column no.2 |
4 | Activated Charcoal with Silver is an antimicrobial, flexible, soft, non-adherent rope which contains an activated charcoal fabric impregnated with silver in a non-woven cover that does not stick to the wound. The device is ideal for packing into deep and tunnel wounds and for use like a wound cover on superficial wounds. 6.5X10 cm, | As per column no.2 |
5 | Activated Charcoal with Silver is an antimicrobial, flexible, soft, non-adherent rope which contains an activated charcoal fabric impregnated with silver in a non-woven cover that does not stick to the wound. The device is ideal for packing into deep and tunnel wounds and for use like a wound cover on superficial wounds. 10X15 cm | As per column no.2 |
6 | Super Absorbent Dressing, sterile, consists of a wound pad of rectangular shape. The clothing protection, the absorbent core and the non- woven distribution layer are of the same size. The multi-layer core of the dressing is covered by a wrapped around wound contact layer, forming wound contact side and back side. This wrapped around layer is glued lengthwise with a blue coloured hot melt-thread forming a tube. Both opposite cutting edges of the wrap are closed with a hot melt adhesive consisting cellulose and polypropylene 10x10 cm, | As per column no.2 |
7 | Super Absorbent Dressing, sterile, consists of a wound pad of rectangular shape. The clothing protection, the absorbent core and the non- woven distribution layer are of the same size. The multi-layer core of the dressing is covered by a wrapped around wound contact layer, forming wound contact side and back side. This wrapped around layer is glued lengthwise with a blue coloured hot melt-thread forming a tube. Both opposite cutting edges of the wrap are closed with a hot melt adhesive consisting cellulose and polypropylene 10x20 cm, | As per column no.2 |
8 | Super Absorbent Dressing, sterile, consists of a wound pad of rectangular shape. The clothing protection, the absorbent core and the non- woven distribution layer are of the same size. The multi-layer core of the dressing is covered by a wrapped around wound contact layer, forming wound contact side and back side. This wrapped around layer is glued lengthwise with a blue coloured hot melt-thread forming a tube. Both opposite cutting edges of the wrap are closed with a hot melt adhesive consisting cellulose and polypropylene 15x20 cm, | As per column no.2 |
9 | Super Absorbent Dressing, sterile, consists of a wound pad of rectangular shape. The clothing protection, the absorbent core and the non- woven distribution layer are of the same size. The multi-layer core of the dressing is covered by a wrapped around wound contact layer, forming wound contact side and back side. This wrapped around layer is glued lengthwise with a blue coloured hot melt-thread forming a tube. Both opposite cutting edges of the wrap are closed with a hot melt adhesive consisting cellulose and polypropylene 20x20 cm, | As per column no.2 |
10 | Super Absorbent Dressing, sterile, consists of a wound pad of rectangular shape. The clothing protection, the absorbent core and the non- woven distribution layer are of the same size. The multi-layer core of the dressing is covered by a wrapped around wound contact layer, forming wound contact side and back side. This wrapped around layer is glued lengthwise with a blue coloured hot melt-thread forming a tube. Both opposite cutting edges of the wrap are closed with a hot melt adhesive consisting cellulose and polypropylene 20x40cm | As per column no.2 |
11 | PHMB Antimicrobial HydroBalance Wound Dressings act against a large spectrum of pathogens. Additionally, depending on the wound condition, the products can either provide the wound with moisture or absorb excess exudate. The product creates a moist wound environment. Dressing change is atraumatic. The material can simply be adjusted to the wound shape and depth. The products are suitable for parts of the body which are difficult to dress. The positive properties of the product counter a possible adhesion to the wound or to the secondary dressing. The moist environment with a cooling effect is perceived as pleasant and soothing by the patients. 5x5 cm, | As per column no.2 |
12 | PHMB Antimicrobial HydroBalance Wound Dressings act against a large spectrum of pathogens. Additionally, depending on the wound condition, the products can either provide the wound with moisture or absorb excess exudate. The product creates a moist wound environment. Dressing change is atraumatic. The material can simply be adjusted to the wound shape and depth. The products are suitable for parts of the body which are difficult to dress. The positive properties of the product counter a possible adhesion to the wound or to the secondary dressing. The moist environment with a cooling effect is perceived as pleasant and soothing by the patients. 9x9 cm, | As per column no.2 |
13 | PHMB Antimicrobial HydroBalance Wound Dressings act against a large spectrum of pathogens. Additionally, depending on the wound condition, the products can either provide the wound with moisture or absorb excess exudate. The product creates a moist wound environment. Dressing change is atraumatic. The material can simply be adjusted to the wound shape and depth. The products are suitable for parts of the body which are difficult to dress. The positive properties of the product counter a possible adhesion to the wound or to the secondary dressing. The moist environment with a cooling effect is perceived as pleasant and soothing by the patients. 14x20 cm, | As per column no.2 |
14 | PHMB Antimicrobial HydroBalance Wound Dressings act against a large spectrum of pathogens. Additionally, depending on the wound condition, the products can either provide the wound with moisture or absorb excess exudate. The product creates a moist wound environment. Dressing change is atraumatic. The material can simply be adjusted to the wound shape and depth. The products are suitable for parts of the body which are difficult to dress. The positive properties of the product counter a possible adhesion to the wound or to the secondary dressing. The moist environment with a cooling effect is perceived as pleasant and soothing by the patients. 2x21cm | As per column no.2 |
15 | Monofilamentous PAD which absorb exudate, cellular debris and keratosis during debridement, gentle on intact tissue. Debridement of superficial, chronic and acute wounds and the skin surrounding the wound. Angled fibre tips remove debris effectively from the wound and preserve already intact tissue; the fibre composite also removes skin flakes and keratosis from skin surrounding the wound; visible results quickly while being easy and safe to use, soft fibres ensure virtually painless application, increasing patient acceptance. | As per column no.2 |
16 | Monofilamentous PAD which absorb exudate, cellular debris and keratosis during debridement, gentle on intact tissue. Debridement of superficial, chronic and acute wounds and the skin surrounding the wound. Angled fibre tips remove debris effectively from the wound and preserve already intact tissue; the fibre composite also removes skin flakes and keratosis from skin surrounding the wound; visible results quickly while being easy and safe to use, soft fibres ensure virtually painless application, increasing patient acceptance. 13x20 cm | As per column no.2 |
17 | Single-use white, cylindrical pad made out of a thick, soft polyester fibre composite of millions of specially angled high-tech fibres on a polypropylene handle for mechanical wound debridement for fast, easy and virtually painless debridement even in hard-to-reach areas and protects intact tissue. Used to absorb exu date, debris and keratodermas during debridement. 160mm | As per column no.2 |
18 | Self-adhesive Superabsorbent Wound Dressing consists of a superabsorber (sodium polyacrylate), which can firmly bind high quantities of wound exudate, imbedded in cellulose and are centrally fixed on an adhesive support layer made of polyurethane and an acrylic based adhesive, intended for the treatment of heavily exuding wounds.12x12 cm | As per column no.2 |
19 | Self-adhesive Superabsorbent Wound Dressing consists of a superabsorber (sodium polyacrylate), which can firmly bind high quantities of wound exudate, imbedded in cellulose and are centrally fixed on an adhesive support layer made of polyurethane and an acrylic based adhesive, intended for the treatment of heavily exuding wounds. 15x15 cm | As per column no.2 |
20 | Self-adhesive Superabsorbent Wound Dressing consists of a superabsorber (sodium polyacrylate), which can firmly bind high quantities of wound exudate, imbedded in cellulose and are centrally fixed on an adhesive support layer made of polyurethane and an acrylic based adhesive, intended for the treatment of heavily exuding wounds. 15x25 cm | As per column no.2 |
21 | Flexible soft Superabsorbent Wound Dressing consists of a superabsorber (sodium polyacrylate), which can firmly bind high quantities of wound exudate, imbedded in cellulose for the treatment of heavily exuding wounds 10x10 cm | As per column no.2 |
22 | Flexible soft Superabsorbent Wound Dressing consists of a superabsorber (sodium polyacrylate), which can firmly bind high quantities of wound exudate, imbedded in cellulose for the treatment of heavily exuding wounds 10x20 cm | As per column no.2 |
23 | Flexible soft Superabsorbent Wound Dressing consists of a superabsorb er (sodium polyacrylate), which can firmly bind high quantities of wound exudate, imbedded in cellulose for the treatment of heavily exuding wounds 20x20 cm | As per column no.2 |
24 | Flexible soft Superabsorbent Wound Dressing consists of a superabsorber (sodium polyacrylate), which can firmly bind high quantities of wound exudate, imbedded in cellulose for the treatment of heavily exuding wounds 20x30 cm | As per column no.2 |
25 | Flexible soft Superabsorbent Wound Dressing consists of a superabsorber (sodium polyacrylate), which can firmly bind high quantities of wound exudate, imbedded in cellulose for the treatment of heavily exuding wounds 7.5x7.5 cm | As per column no.2 |
26 | Antimicrobial Calcium Alginate Wound Dressing are soft & conformable wound covers with high mannuronic acid. 5x5cm | As per column no.2 |
27 | Antimicrobial Calcium Alginate Wound Dressing are soft & conformable wound covers with high mannuronic acid. 10x20cm | As per column no.2 |
28 | Antimicrobial Calcium Alginate Wound Dressing are soft & conformable wound covers with high mannuronic acid. 10x10cm | As per column no.2 |
29 | Hydro-Balance wound dressing can either provide the wound with moisture or can absorb the exces exudate. It creates moist wound enviroment which maintains the cooling effect and it can adjust to wound shape and size. 5x5cm | As per column no.2 |
30 | Hydro-Balance wound dressing can either provide the wound with moisture or can absorb the exces exudate. It creates moist wound enviroment which maintains the cooling effect and it can adjust to wound shape and size. 9x9cm, | As per column no.2 |
31 | Hydro-Balance wound dressing can either provide the wound with moisture or can absorb the exces exudate. It creates moist wound enviroment which maintains the cooling effect and it can adjust to wound shape and size.14x20cm; | As per column no.2 |
32 | Hydro-Balance wound dressing can either provide the wound with moisture or can absorb the exces exudate. It creates moist wound enviroment which maintains the cooling effect and it can adjust to wound shape and size. 2x21cm | As per column no.2 |
33 | Super absorbent wound dressing for both acute & Cronic wounds made up of polyethylene, polypropylene, cellulose,polypropylene terephthalate,ethylene,vinyl acetate copolymer,polyacrylate. 10x10cm; | As per column no.2 |
34 | Super absorbent wound dressing for both acute & Cronic wounds made up of polyethylene, polypropylene, cellulose,polypropylene terephthalate,ethylene,vinyl acetate copolymer,polyacrylate. 12.5x12.5cm; | As per column no.2 |
35 | Super absorbent wound dressing for both acute & Cronic wounds made up of polyethylene, polypropylene, cellulose,polypropylene terephthalate,ethylene,vinyl acetate copolymer,polyacrylate. 22x22cm; | As per column no.2 |
36 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Unmeshed form 2x2 cm | As per column no.2 |
37 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Unmeshed form 4x4 cm | As per column no.2 |
38 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Unmeshed form 5x7 cm | As per column no.2 |
39 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Unmeshed form 6x7 cm | As per column no.2 |
40 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Unmeshed form 4x8 cm | As per column no.2 |
41 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 2x2 cm | As per column no.2 |
42 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 3x3 cm | As per column no.2 |
43 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 4x4 cm | As per column no.2 |
44 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 5x7 cm | As per column no.2 |
45 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 6x7 cm | As per column no.2 |
46 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 4x8 cm | As per column no.2 |
47 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 4x8 cm | As per column no.2 |
48 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 5x9 cm | As per column no.2 |
49 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 8x10 cm | As per column no.2 |
50 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 8x12 cm | As per column no.2 |
51 | Advanced human acellular dermal matrix with 97% of donor DNA removed and sterility assurance level of 10¯6 allowing for rapid cellular infiltration and re-vascularization for the treatment of chronic wounds as well as burn management and for soft tissue reconstruction. Meshed form 6x10 cm | As per column no.2 |
52 | Electrolysed Non-Toxic, Non-Irritant and Non- Corrosive, Ready to use Disinfectant Solution with Neutral pH containing Sodium Chloride (Na Cl)- )0.023%, Sodium Hypochlorite (NaOCl)- 0.005%, Hypo Chlorous Acid (HOCl)- 0.004%, Electrolysed Water- 99.97% in Spray Bottle of 1000ml | As per column no.2 |
53 | Electrolysed Non-Toxic, Non-Irritant and Non- Corrosive, Ready to use Disinfectant Solution with Neutral pH containing Sodium Chloride (NaCl)- )0.023%, Sodium Hypochlorite (NaOCl)- 0.005%, Hypo Chlorous Acid (HOCl)- 0.004%, Electrolysed Water- 99.97% in Refill Bottle of 1000ml | As per column no.2 |
54 | Electrolysed Non-Toxic, Non-Irritant and Non- Corrosive, Ready to use Disinfectant Solution with Neutral pH containing Sodium Chloride (Na Cl)- )0.023%, Sodium Hypochlorite (NaOCl)- 0.005%, Hypo Chlorous Acid (HOCl)- 0.004%, Electrolysed Water- 99.97% in Jerricane of 5 Litre | As per column no.2 |
55 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive/slit to conform around the PIV Hub. Size 6cmX7cm | As per column no.2 |
56 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive. Size 6cmX7cm | As per column no.2 |
57 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive. Size 10cmX12cm | As per column no.2 |
58 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/ one half laminated with soft cloth breathable backing for enhanced grip/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive. Size 5cmX5.7cm | As per column no.2 |
59 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/ one half laminated with soft cloth breathable backing for enhanced grip/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive/slit to conform around the PIV Hub. Size 7cmX8.5cm | As per column no.2 |
60 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/ one half laminated with soft cloth breathable backing for enhanced grip/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive/slit to conform around the CVC Hub. Size 8.5cmX10.5cm | As per column no.2 |
61 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free), Reinforced border, deep notch, and tape strips work together to enlist the entire dressing in securement. They are covered with a waterproof film to prevent strikethrough, Pattern Coated Adhesive hold strongly, manage moisture, and release easily, Designed to maintain securement by preventing edge lift, flexing with patient movement, and managing moisture, Can potentially reduce the number of dressing changes and restarts - May be worn for up to 7 days on a PIV catheter, Easy to apply and remove, Designed to promote consistent application, Frame delivery makes placement accurate and easy, Supports infection prevention goals - A waterproof film coating on all pieces provides a barrier to external contaminants including liquids, bacteria and viruses* - Allows continuous monitoring, It is coated with water repellent hypo-allergic pressure sensitive acrylate adhesive; CHG Wipe : CDC Compliant Skin prep (Best Practices), Results faster bacteria kill and residual action for effective infection control, Broad spectrum activity against bacteria and virus; Sterile packaged gauze piece: Non-woven Dry gauze in a separate packaging for controlling backflash and maintains asepsis; Tourniquet: Non-reusable and non – carrier of infections between patients and healthcare workers. 12.7cm x 19.5 cm | As per column no.2 |
62 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/Reinforced border, deep notch, and tape strips work together to enlist the entire dressing in securement/pattern coated adhesive hold strongly, manage moisture/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive/slit to conform around the PIV Hub. Size 6.5cmX7cm | As per column no.2 |
63 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/Reinforced border, deep notch, and tape strips work together to enlist the entire dressing in securement/pattern coated adhesive hold strongly, manage moisture/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive/slit to conform around the CVC Hub. Size 8.5cmX11.5cm | As per column no.2 |
64 | Single, Sterile,Virus proof,polyurethane film,pressure sensitive Acrylate adhesive for CVC applications with CHG gel pad which has Unique composition of water, polymers and 2% chlorhexidine gluconate. Chlorhexidine Gluconate Dressing for CVP 8.5cm X11.5cm | As per column no.2 |
65 | Single, Sterile,Virus proof,polyurethane film,pressure sensitive Acrylate adhesive for CVC applications with CHG gel pad which has Unique composition of water, polymers and 2% chlorhexidine gluconate. Chlorhexidine Gluconate Dressing for CVP 7cmX8.5cm | As per column no.2 |
66 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive. Size 10cmX25cm | As per column no.2 |
67 | Single, Sterile, Transparent, Semi-permeable thin conformable polyurethane film (latex free)/ one half laminated with soft cloth breathable backing for enhanced grip/ water, virus and bacteria proof/coated with water repellent hypo-allergic pressure sensitive acrylate adhesive. Size 3.8 CM X 4.5 CM | As per column no.2 |
68 | Disinfecting Cap for Needleless Connectors Individuals | As per column no.2 |
69 | Disinfecting Cap Strip for Needleless Connectors Strip -10 Count | As per column no.2 |
70 | Disinfecting Cap Strip for Male Luers | As per column no.2 |
71 | Disinfecting Cap for Tego® Hemodialysis Connectors | As per column no.2 |
72 | An alcohol-free liquid barrier film containing acrylate terpolymer, Polyphenylmethylsiloxane, Hexamethyldisoloxane and Isooctane which dries quickly to form a breathable, transparent, hypoallergenic, non-cytotoxic coating to protect damaged or intact skin from friction, moisture, shear, bodily fluids, incontinence and adhesive trauma. Size 1ml | As per column no.2 |
73 | An alcohol-free liquid barrier film containing acrylate terpolymer, Polyphenylmethylsiloxane, Hexamethyldisoloxane and Isooctane which dries quickly to form a breathable, transparent, hypoallergenic, non-cytotoxic coating to protect damaged or intact skin from friction, moisture, shear, bodily fluids, incontinence and adhesive trauma. Size 3ml | As per column no.2 |
74 | Antimicrobial Skin Cleansing Wipes for sponging Patients in ICU, Bed ridden Patients 32CM X 30CM | As per column no.2 |
75 | Waterless CHG and alcohol based handrub for hand Hygiene, Uniquely formulated - Chlorhexidine Gluconate IP 2.5% v/v (equivalent to 0.5% w/v Chlorhexidine Gluconate) and Ethanol IP 70% v/v with moisturizer and emollients to be used with a twin purpose wall mount/bed-side dispenser. Broad Spectrum Antimicrobial. | As per column no.2 |
76 | Rechargeable Surgical Clipper with fixed head and Cutting disposable blade, run time of 180 minutes., rechargeable NiCad Battery with cordless charger. Ergonomic, non-slip clipper handle fits comfortably in hand. Removes all types of head and body hair-fine or coarse, wet or dry. Single use blades snap on and pop off easily, reducing the risk of cross- contamination. Handle can be cleaned quickly and easily with a disinfectant or by submersing in water. Certified by UL | As per column no.2 |
77 | Incisde drape made up of Polyester film with an acrylic adhesive that contains a complex of iodoform(N- vinyl 2 pyrrolidine) with a iodine concentration of 0.092 mg Iodine/cm2. Film should be breathable and conformable to skin, compatible with Povidone and CHG skin preps. Iodine from the drape should be present in the deepest skin layers (1000 microns depth) where hair folices exist apart from killing microbes on skin layer. Incise Area : 34 cm x 35 cm | As per column no.2 |
78 | Incisde drape made up of Polyester film with an acrylic adhesive that contains a complex of iodoform(N- vinyl 2 pyrrolidine) with a iodine concentration of 0.092 mg Iodine/cm2. Film should be breathable and conformable to skin, compatible with Povidone and CHG skin preps. Iodine from the drape should be present in the deepest skin layers (1000 microns depth) where hair folices exist apart from killing microbes on skin layer.Incise Area : 56cm x 45cm | As per column no.2 |
79 | Incisde drape made up of Polyester film with an acrylic adhesive that contains a complex of iodoform(N- vinyl 2 pyrrolidine) with a iodine concentration of 0.092 mg Iodine/cm2. Film should be breathable and conformable to skin, compatible with Povidone and CHG skin preps. Iodine from the drape should be present in the deepest skin layers (1000 microns depth) where hair folices exist apart from killing microbes on skin layer. Incise Area : 10cm x 20cm | As per column no.2 |
80 | Incise drape made up of Polyester film with an acrylic adhesive that contains a complex of iodoform(N- vinyl 2 pyrrolidine) with a iodine concentration of 0.092 mg Iodine/cm2. Film should be breathable and conformable to skin, compatible with Povidone and CHG skin preps. Iodine from the drape should be present in the deepest skin layers (1000 microns depth) where hair folices exist apart from killing microbes on skin layer 30CM x 30CM | As per column no.2 |
81 | Incise Drape which is Antimicrobial, strong, conformable and breathable Iodophor impregnated Polyester film coated with hypoallergenic adhesive for superior adhesion. Contains a Framed delivery system for one-person drape application, designed specifically for minimally invasive surgical procedure.Compatible with Povidine Iodine & CHG Preps.Latex Free.26CM x 20CM | As per column no.2 |
82 | Incisde drape made up of Polyester film with an acrylic adhesive that contains a complex of iodoform(N- vinyl 2 pyrrolidine) with a iodine concentration of 0.092 mg Iodine/cm2. Film should be breathable and conformable to skin, compatible with Povidone and CHG skin preps. Iodine from the drape should be present in the deepest skin layers (1000 microns depth) where hair folices exist apart from killing microbes on skin layer. 56cm x 60cm | As per column no.2 |
83 | Waterless alcohol based handrub for hand Hygiene, Uniquely formulated (2- propanol – 45% w/w, 1- propanol – 30%w/w, Ethyl – hexadecyl – dimethyl ammonium sulphate – 0.2 w/w, with emollient & moisturizer to be used with a twin purpose wall mount/bed-side dispenser. Broad Spectrum Antimicrobial (Bactericidal, Sporicidal, Fungicidal, Virucidal). | As per column no.2 |
84 | Waterless CHG and alcohol based handrub for hand Hygiene, Uniquely formulated - Chlorhexidine Gluconate IP 2.5% v/v (equivalent to 0.5% w/v Chlorhexidine Gluconate) and Ethanol IP 70% v/v with moisturizer and emollients. Broad Spectrum Antimicrobial. | As per column no.2 |
85 | CHG is found to bind better to the stratum corneum (or the outermost layer of skin, acting as a barrier to keep bacteria out and hold moisture in) providing for a longer duration of anti-microbial action. Fully documented compliance with the following supported by Govt certified Labs or Third Party Labs certification: ISO 10993 Part 10,2010 : Test for Irritation and Skin Sensitization,EN1040-2005 : Bactericidal and EN 1275-2005 : Yeasticidal,USP-36 Disinfectant and Antiseptics 1072:2013 Fungicidal and Sporicidal, HCIPT (Human cumulative irritancy patch test. Appraised efficacy in compliance with ASTM Test method # 2315, Recommended for use in medical applications - Polyurethanes can outperform many other materials in flexibility, tear resistance and abrasion resistance. Open cell foam – common benefits of this material is they are soft and breathable, more flexible and returns easily to its original state after compressing. High Density of 28.8 to 35.2 kg/m3 – Higher resilience and commonly withstands high usage | As per column no.2 |
86 | Surgical skin prepping antiseptic solution, Uniquely formulated - Povidone-Iodine IP 10% w/v (equivalent to 1% w/v available iodine) Water IP qs. Broad Spectrum Antimicrobial (Bactericidal, Sporicidal, Fungicidal, Virucidal). | As per column no.2 |
87 | Chlorhexidine Gluconate Scrub Solution 4% w/v (equivalent to 20% v/v) - Broad Spectrum (Bactericidal, Fungicidal, Virucidal and Sporicidal) antimicrobial solution for surgical scrubbing and pre-operative patient showering, in a translucent bottle with volume calibration,500ml | As per column no.2 |
88 | Non woven 3 layered Sterile, lightweight, breathable and low linting Surgical Disposable Gown with Alocohol Repellant & Anti Static fabric. Made of 43 gsm fabric with Alcohol Repellancy (AATCC193-2012) level 8. Low linting, indivually sterile packed with 2 absorbent paper towels. Size XL- 137 cm (L) * 160 cm(W) | As per column no.2 |
89 | Surgical hand and skin scrubbing antiseptic solution, Uniquely formulated - Povidone-Iodine IP 7.5% w/v (equivalent to 0.75% w/v available iodine) Water IP qs. Broad Spectrum Antimicrobial (Bactericidal, Sporicidal, Fungicidal, Virucidal). | As per column no.2 |
90 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003,A basic surgical pack with the above features should contain 2nos of cautery bags(size 30cm x 35cm), 1no of operation tape(size 10cm x 55cm), 4nos of hand towels(23.5cm x 38cm), 2nos of adhesive towel drape(size 91.5cm x 100cm), 1no of adhesive medium drape sheet(size 183cm x 183cm), 1no of adhesive large drape sheet(size 150cm x 250cm), 1no of instrument table cover(150cm x 200cm), 1no of large instrument table cover(size 183cm x 240cm) | As per column no.2 |
91 | Broad spectrum virucidal, bactericidal and fungicidal waterless alcohol based hand- rub for hand hygiene, containing 75% v/v Iso-propyl Alcohol, moisturizer and emollients with a wall-mounting/bed-side stand,500ml | As per column no.2 |
92 | Waterless alcohol based handrub for hand Hygiene, Uniquely formulated (2- propanol – 45% w/w, 1- propanol – 30%w/w, Ethyl – hexadecyl – dimethyl ammonium sulphate – 0.2 w/w, with emollient & moisturizer. Broad Spectrum Antimicrobial (Bactericidal, Sporicidal, Fungicidal, Virucidal),100ML | As per column no.2 |
93 | Chlorhexidine Gluconate Scrub Solution 2% w/v (equivalent to 10% v/v) – Broad spectrum (Bactericidal, Fungicidal, Virucidal and Sporicidal) antimicrobial solution for skin preparation in a translucent bottle with volume calibration,100ml | As per column no.2 |
94 | Product must be made of low-linting, nonwoven, absorbent fabric laminated to a plastic film. Must be resistant to fluid strikethrough. Must be absorbent throughout the entire drape, this eliminating the need to define a “critical zoneâ€. Must meet Flammability Class 1 (CFR Title 16 Part 1610). Components include: Cautery Bags (30cm x 35cm) - 4 Nos, Operation Tapes (10cm x 55cm) - 3 No, Hand Towels - (23.5cm x 38cm) - 4 Nos, Adhesive Towel Drapes - (91.5cm x 100cm) - 4 Nos, Adhesive Drape sheet (M) - (183cm x 183cm) - 1 No, Adhesive Drape Sheet (L) - (150cm x 250cm) - 1 No, Instrument Table cover - (150cm x 200cm) - 1 No, Instrument Table Cover (L) - (183cm x 240cm) - 1 No, Bilateral Split Sheet - (183cm x 200cm) - 1 No, Triangular Drape Sheets - (91.5cm x 91.5cm x 129cm) - 2 Nos | As per column no.2 |
95 | Surgical skin prepping antiseptic solution, Uniquely formulated - Povidone-Iodine IP 5% w/v (equivalent to 0.5% w/v available iodine) Water IP qs. Broad Spectrum Microbicidal Solution (Bactericidal, Sporicidal, Fungicidal). | As per column no.2 |
96 | Waterless CHG and alcohol based handrub for hand Hygiene, Uniquely formulated - Chlorhexidine Gluconate IP 2.5% v/v (equivalent to 0.5% w/v Chlorhexidine Gluconate) and Ethanol IP 70% v/v with moisturizer and emollients. Broad Spectrum Antimicrobial,100ML | As per column no.2 |
97 | Non woven 3 layered Sterile, lightweight, breathable and low linting Surgical Disposable Gown with Alocohol Repellant & Anti Static fabric. Made of 43 gsm fabric with Alcohol Repellancy (AATCC193-2012) level 8. Low linting, indivually sterile packed with 2 absorbent paper towels. Size L - 132 cm (L) * 150 cm (W) | As per column no.2 |
98 | A transparent and a clear Drape that should provide a reliable barrier to bacteria on the skin. Must come equipped with a reliable and secure adhesive and should be available at 10 units per pack. Length must be 23 inch and width must be 17 inches. Must be ISO certified | As per column no.2 |
99 | Chlorhexidine Gluconate Scrub Solution 4% w/v (equivalent to 20% v/v) - Broad Spectrum (Bactericidal, Fungicidal, Virucidal and Sporicidal) antimicrobial solution for surgical scrubbing and pre-operative patient showering, in a translucent bottle with volume calibration,100ml | As per column no.2 |
100 | Non woven 4 layered Sterile, lightweight, breathable and low linting Surgical Disposable Gown with Outer and Inner layer made of strong and spun bond repellent fabric, and two middle layers offering fluid control and bacterial barrier. CE certified, Tvyek outer packaging. | As per column no.2 |
101 | Waterless alcohol based handrub for hand Hygiene, Uniquely formulated (2- propanol – 45% w/w, 1- propanol – 30%w/w, Ethyl – hexadecyl – dimethyl ammonium sulphate – 0.2 w/w, with emollient & moisturizer. Broad Spectrum Antimicrobial (Bactericidal, Sporicidal, Fungicidal, Virucidal),100ml With Pump | As per column no.2 |
102 | Surgical hand and skin scrubbing antiseptic solution, Uniquely formulated - Povidone-Iodine IP 7.5% w/v (equivalent to 0.75% w/v available iodine) Water IP qs. Broad Spectrum Antimicrobial (Bactericidal, Sporicidal, Fungicidal, Virucidal),100ml | As per column no.2 |
103 | Sterile Isolation Bag composed of Ethyl Methyl Acrylate (EMA) film with Polyester Drawstring closure. Can be used in sterile field to isolate and contain organs and body parts for surgical procedures. 20 inches x 20 inches (50 cm x 50 cm) | As per column no.2 |
104 | Waterless CHG and alcohol based handrub for hand Hygiene, Uniquely formulated - Chlorhexidine Gluconate IP 2.5% v/v (equivalent to 0.5% w/v Chlorhexidine Gluconate) and Ethanol IP 70% v/v with moisturizer and emollients. Broad Spectrum Antimicrobial. | As per column no.2 |
105 | Waterless Foam based CHG and alcohol based handrub for hand Hygiene, Uniquely formulated - Chlorhexidine Gluconate IP 2.5% v/v (equivalent to 0.5% w/v Chlorhexidine Gluconate) and Ethanol IP 70% v/v with moisturizer and emollients with unique drip resistant dispenser design. Broad Spectrum Antimicrobial,500ml | As per column no.2 |
106 | Product must be made of low-linting, nonwoven, absorbent fabric laminated to a plastic film. Must be resistant to fluid strikethrough. Must be absorbent throughout the entire drape, this eliminating the need to define a “critical zoneâ€. Must meet Flammability Class 1 (CFR Title 16 Part 1610). Components Include: Adhesive Drape Sheet - (228cm x 330cm) - 1 No | As per column no.2 |
107 | Transparent, conformable, strike proof, matte finish, and plastic polyethylene split sheet with U- Aperture cut in one end of drape, to isolate (operative area) sterile field from unclean area. U-Aperture coated with a Pressure sensitive adhesive lining for secural. | As per column no.2 |
108 | Chlorhexidine Gluconate Scrub Solution 2% w/v (equivalent to 10% v/v) – Broad spectrum (Bactericidal, Fungicidal, Virucidal and Sporicidal) antimicrobial solution for skin preparation in a translucent bottle with volume calibration,100ml | As per column no.2 |
109 | FDA approved waterless, brushless, scrubless CHG & Ethanol based surgical hand antiseptic with moisturizers containing Chlorhexidine Gluconate 1% w/w and Ethyl Alcohol 61% w/w supplied with a foot pump for touchless delivery with 500ml Pack Size | As per column no.2 |
110 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003 | As per column no.2 |
111 | Transparent, conformable, strike proof, matte finish, and plastic polyethylene split sheet with U- Aperture cut in one end of drape, to isolate (operative area) sterile field from unclean area. U-Aperture coated with a Pressure sensitive adhesive lining for secural. | As per column no.2 |
112 | Waterless Foam based CHG and alcohol based handrub for hand Hygiene, Uniquely formulated - Chlorhexidine Gluconate IP 2.5% v/v (equivalent to 0.5% w/v Chlorhexidine Gluconate) and Ethanol IP 70% v/v with moisturizer and emollients with unique drip resistant dispenser design. Broad Spectrum Antimicrobial,50ml | As per column no.2 |
113 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003 and ISO 9001:2008. The pack with above features should contain 1no of Bilateral Knee Drape (size 300cm x 370cm). | As per column no.2 |
114 | Surgical skin prepping antiseptic solution, Uniquely formulated - Povidone-Iodine IP 5% w/v (equivalent to 0.5% w/v available iodine) Water IP qs. Broad Spectrum Microbicidal Solution (Bactericidal, Sporicidal, Fungicidal),100ml | As per column no.2 |
115 | Non woven 3 layered Sterile, lightweight, breathable and low linting Surgical Disposable Gown with Alocohol Repellant & Anti Static fabric. Made of 43 gsm fabric with Alcohol Repellancy (AATCC193-2012) level 8. Low linting, indivually sterile packed with 2 absorbent paper towels. | As per column no.2 |
116 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003 and ISO 9001:2008. A Hip Drape with above features should contain 2nos of cautery bags(size 30cm x 35cm), 3no of operation tape(size 10cm x 55cm), 4nos of hand towels(23.5cm x 38cm), 1no of Adhesive split sheet (size 228cm x 260cm), 1no of Hip drape (size 300cm x 353cm), 1no of instrument table cover(150cm x 200cm), 1no of large instrument table cover(size 183cm x 240cm). | As per column no.2 |
117 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003 and ISO 9001:2008. The pack with above features should contain 2nos of cautery bags(size 30cm x 35cm), 3no of operation tape(size 10cm x 55cm), 4nos of hand towels(23.5cm x 38cm), 1no of adhesive medium drape sheet(size 183cm x 183cm), 1no of adhesive large drape sheet(size 150cm x 250cm), 1no of instrument table cover(150cm x 200cm), 1no of Adhesive split sheet (size 228cm x 260cm). | As per column no.2 |
118 | Waterless CHG and alcohol based handrub for hand Hygiene, Uniquely formulated - Chlorhexidine Gluconate IP 2.5% v/v (equivalent to 0.5% w/v Chlorhexidine Gluconate) and Ethanol IP 70% v/v with moisturizer and emollients to be used with a twin purpose wall mount/bed-side dispenser. Broad Spectrum Antimicrobial.500ML | As per column no.2 |
119 | Waterless CHG and alcohol based handrub for hand Hygiene, Uniquely formulated - Chlorhexidine Gluconate IP 2.5% v/v (equivalent to 0.5% w/v Chlorhexidine Gluconate) and Ethanol IP 70% v/v with moisturizer and emollients. Broad Spectrum Antimicrobial.100ML | As per column no.2 |
120 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003 and ISO 9001:2008. An Extremity Drape sheet with above features should contain 1no of adhesive extremity drape sheet(size 228cm x 330cm). | As per column no.2 |
121 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003 and ISO 9001:2008. The pack with above features should contain 1no of Arthroscopy Sheet with Pouch (size 292cm x 304cm). | As per column no.2 |
122 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003 and ISO 9001:2008. The pack with above features should contain 1no of Stockinet (size 121cm x 30cm). | As per column no.2 |
123 | Broad spectrum virucidal, bactericidal and fungicidal waterless alcohol based hand- rub for hand hygiene, containing 75% v/v Iso-propyl Alcohol, moisturizer and emollients with a wall-mounting/bed-side stand.100ml | As per column no.2 |
124 | High barrier disposable surgical drapes made of reinforced spunbond-film composite which is a blue laminate of polypropylene nonwoven and a polyethylene film offering absorbency yet imperviousness to fluid strike-through across the entire drape material. It should be low-linting, non-breathable with an adhesive area, wherever incorporated, containing hypoallergenic acrylate type adhesive covered with a silicone coated paper liner and should also comply with the requirements of ISO 13485:2003 and ISO 9001:2008. The pack with above features should contain 2nos of adhesive drape sheet (size 91.5cm x 100cm). | As per column no.2 |
125 | Incise Drape which is Antimicrobial, strong, conformable and breathable Iodophor impregnated Polyester film coated with hypoallergenic adhesive for superior adhesion. Contain a clear plastic, fluid collection pouch around the incise drape. Compatible with Povidine Iodine & CHG Preps.Latex Free,42 cm * 52 cm | As per column no.2 |
126 | Product must be made of low-linting, nonwoven, absorbent fabric laminated to a plastic film. Must be resistant to fluid strikethrough. Must be absorbent throughout the entire drape, this eliminating the need to define a “critical zoneâ€. Must meet Flammability Class 1 (CFR Title 16 Part 1610). Components Include: Under arm sheet (114cm x 100cm) - 1 No, Operation Tapes (10cm x 55cm) - 2 No, Triangular Drape Sheets - (91.5cm x 91.5cm x 129cm) - 2 Nos | As per column no.2 |
127 | Surgical drape that provides a vertical barrier to keep the C-arm isolated from the sterile surgical field with a strong polyethylene film to withstand heavy manipulation during use of the fluoroscope ensuring aseptic conditions during surgery. Must be a one piece design with a clear plastic film allows for visualisation of the fluoroscope during the operation. Must have Instrument pouches and tube organisers to keep wires and tubes and instruments out of the operative side and a filter screen that catches bone chips and tissue for specimen. Must be Latex-free for patient and healthcare worker safety. Dimensions - Overall: 320cm x 213cm; Incise area: 48cm x 25cm; 5 units per case. Must have ISO Certification | As per column no.2 |
128 | • Self contained vials of Spore strip B. Stero-thermophilus population • Test tube containing Modified Soy Tryptic Broth as growth medium with Bromocresol Purple Dye • Easily identifiable color change to yellow in case of Bacterial Growth within 48 hrs or before after incubating at 56 degree C temperature. Should be compliant to ISO 11138-1:2006(en) Part 1 and ISO 11138-1:2006(en) Part 3 • ANSI/AAMI/ ISO 11138-1:2006 & 11138-3: 2006 • Should have a BSI Kitemark Certificate • Every box should contain Quality Assurance certificate with mention of Spore population & D- value | As per column no.2 |
129 | • Self contained vials of Spore strip B. Atropheus population • Test tube containing Modified Soy Tryptic Broth as growth medium with Brothymol Blue Dye • Easily identifiable color change in case of Bacterial Growth within 48 hrs or before after incubating at 37 degree C temperature. Should be compliant to ISO 11138-1:2006(en) Part 1 and ISO 11138-1:2006(en) Part 2 • ANSI/AAMI/ ISO 11138-1:2006 & 11138-2: 2006 • Should have a BSI Kitemark Certificate • Every box should contain Quality Assurance certificate with mention of Spore population & D- value | As per column no.2 |
130 | • Rapid readout biological indicators containing a standardized, viable population of Bacillus Atropheus spores for ETO Sterilization Cycles • The indicator detects the presence of viable spores by the production of fluorescence within 4 hours in conjunction with Rapid Readout Incubator • Designed and certified as per ISO 11138 and EN 866.• Should be compliant to ISO 11138-1:2006(en) Part 1 and ISO 11138-1:2006(en) Part 2 • Every box should contain Quality Assurance certificate with mention of Spore population, D- value & Z value • Should have a BSI Kitemark Certificate • Should have FDA clearance | As per column no.2 |
131 | • Rapid readout biological indicators for steam sterilization containing a standardized, viable population of Bacillus stearothermophilus spores • The indicator detects the presence of viable spores by the production of fluorescence in 3 hours in conjunction with Rapid Readout Incubator • Designed and certified as per ISO 11138 and EN 866. • Should be compatible with the following cycles: a) 121-123°C gravity steam sterilization Cycle b) 132-135°C vacuum-assisted steam sterilization cycles. Should be compliant to ISO 11138-1:2006(en) Part 1 and ISO 11138-1:2006(en) Part 3 • Every box should contain Quality Assurance certificate with mention of Spore population, D- value & Z value • Should have a BSI Kitemark Certificate • Should have FDA clearance | As per column no.2 |
132 | • Lead free • Heat sensitive chemical indicator self adherent tape • Should not leave any adhesive residue, for Steam Sterilization cycles. • Color change should be from white to dark brown for easy identification after processed in Steam Autoclaves of different time and temperature requirements, within 15 minutes at 121 degree C and 3 minutes at 134 degree C.•Class 1: Confirms to ANSI/ AAMI/ ISO 11140-1: 2005 • Certificate of Analysis should be available for every batch • Should have FDA clearance | As per column no.2 |
133 | • Test Packs for monitoring Vacuum formation in Autoclave chambers. • Test sheet along with penetration challenge material should be in a single easy handled pack. • Should be lead free. • Weight per pack should be 110 to 125 gms.Should be compliant to ANSI/AAMI/ISO 11140-1:20051 • Should be compliant to ANSI/AAMI/ISO 11140-5:20072 | As per column no.2 |
134 | The 3Mâ„¢ Complyâ„¢ Steam Chemical Indicator 1250 offers an off-white to black color change when exposed to steam sterilization. Can be used in all 121- 134°C (250-273°F) gravity and vacuum assisted steam sterilization cycles. The strip is perforated, allowing full or half-length use for different pack sizes. After processing, the chemical indicator line will turn from off-white to black when exposed to steam sterilization. Strip is perforated enabling full or half-length usage depending on pack size. 3Mâ„¢ Comply Steam Chemical Indicator 1250 is designed to monitor all 121-134°C (250-273° F) gravity and vacuum assisted steam sterilization cycles. •T ype 4 (category i4) internal indicators as categorized by ISO 11140-1:2014 •Two year shelf life | As per column no.2 |
135 | The 3Mâ„¢ Complyâ„¢ 1251 EO Chemical Indicator Strip as an internal pack process indicator to monitor all warm and cool cycles of 100% EO and EO/HCFC (hydrochlorofluorocarbon) gas mixture sterilizer cycles. The chemical indicator bar turns from red to green when exposed to critical parameters of the EO sterilization process (i.e., gas concentration RH, time and temperature). Designed to monitor all warm and cool cycles of 100% EO and EO/HCFC (hydrochlorofluorocarbon) gas mixture sterilizer cycles Strip is perforated enabling full or half-length usage depending on pack size Two year shelf life | As per column no.2 |
136 | • Moving front Chemical integrators, indicating Accept or Reject, to verify all perimeters of steam sterilization together i.e. Time, Temperature and Quality of steam. • Can be used for pack control monitoring of all 118-138ºC (245-280ºF) steam sterilization cycles Should be compliant to BS/ EN/ ISO 11140-1: 2005 • Should have 510 (k) registration • Should have a BSI Kitemark Certificate | As per column no.2 |
137 | • Multiple enzymatic concentrate solution with lipases, cellulases, proteases and amylases • Must act against all possible body secretions, compatible to all instruments • Fast acting within 2- 10 minutes, allow safe disposable via the drain after use • Leaves no residue after wash, Stable formulation with near neutral pH. Compliance to ISO 13485, 1 L | As per column no.2 |
138 | • Multiple enzymatic concentrate solution with lipases, cellulases, proteases and amylases • Must act against all possible body secretions, compatible to all instruments • Fast acting within 2- 10 minutes, allow safe disposable via the drain after use • Leaves no residue after wash, Stable formulation with near neutral pH. Compliance to ISO 13485, 100ML | As per column no.2 |
139 | Label thickness 0.2 mm (± 0.01mm) Label dimension 32x28mm Release layer material should be Semi bleached kraft paper Visual Appearance: 1) Corner cut piggy back label 2) 2) White colored paper label Double liner Labels: Release paper thickness Liner 1 Paper should be 0.05 mm (± 0.01mm) (1.97 mil) Release paper thickness Liner 2 Paper should be 0.06 mm (± 0.01mm) (2.36 mil) | As per column no.2 |
140 | Label thickness 0.2 mm (± 0.01mm) Label dimension 32x28mm Release layer material should be Semi bleached kraft paper Visual Appearance: 1) Corner cut piggy back label 2) 2) White colored paper label Double liner Labels: Release paper thickness Liner 1 Paper should be 0.05 mm (± 0.01mm) (1.97 mil) Release paper thickness Liner 2 Paper should be 0.06 mm (± 0.01mm) (2.36 mil) | As per column no.2 |
141 | • Multiple enzymatic concentrate solution with lipases, cellulases, proteases and amylases • Film based Polymer technology with controlled enzyme release • Must act against all possible body secretions, compatible to all instruments • Fast acting within 2- 10 minutes, allow safe disposable via the drain after use • Leaves no residue after wash, Stable formulation with near neutral pH. • Should have scale inhibition properties • Should help retain shine of the instrument • Should be usable for manual, ultra sonic and automatic cleaning systems • Properties should have been tested by methods prescribed by NACE TM0374:2007 & NACE TM0169/ ASTM G31: 2012,Compliance to ISO 13485 | As per column no.2 |
142 | • Super Rapid readout biological indicators for plasma sterilization containing a standardized, viable population of Bacillus stearothermophilus spores • The indicator detects the presence of viable spores by the production of fluorescence in 24 mins in conjunction with 490 autoreader or 490M autoreader. •U se the 3Mâ„¢ Attestâ„¢ Rapid Readout Biological Indicator 1295 in conjunction with the 3Mâ„¢ Attestâ„¢ Auto-reader as a standard method of routine monitoring of vaporized hydrogen peroxide sterilization processes in the following systems: AMSCO® V-PRO® 1 Low Temperature Sterilization System (Lumen cycle), AMSCO® V-PRO® 1 Plus Low Temperature Sterilization System (Lumen and Non Lumen cycles), AMSCO® V-PRO® maX Low Temperature Sterilization System (Lumen, Non Lumen, and Flexible cycles), AMSCO® V-PRO® 60 Low Temperature Sterilization System (Lumen, Non Lumen and Flexible cycles) and in STERRAD® 100S, STERRAD® NX (Standard and Advanced cycles), STERRAD® 100NX (Standard, Flex, Express and Duo cycles) systems, STERRAD® NX with AllClearâ„¢ Technology (Standard and Advanced cycles) and STERRAD® 100NX with AllClearâ„¢ Technology (Standard, Flex, Express and Duo cycles). | As per column no.2 |
143 | • Equipment should show remaining minutes left of BI incubation. • Should be able to Configure Auto-reader remotely from a PC. • Should have a built-in web app to allow create documentation that can be printed or saved electronically. • Shold have an option to connect to select sterile processing instrument tracking systems. • Auto reader, self calibrating, to read Rapid Attest BI, with ten incubation wells • Positive BI Read-out time within 4 hrs by an audible alarm. Should have IEC 61326-1 Electrical equipment for measurement, control and laboratory us+C11e -EMC requirements - Part 1: General requirements • Should Comply with the EMC requirements of the CE mark EMC Directive 2004/108/EC. | As per column no.2 |
144 | • Equipment should show remaining minutes left of BI incubation. • Should be able to Configure Auto-reader remotely from a PC. • Should have a built-in web app to allow create documentation that can be printed or saved electronically. • Shold have an option to connect to select sterile processing instrument tracking systems. • Auto reader, self calibrating, to read Rapid Attest BI, with ten incubation wells • Positive BI Read-out time of 1 hr to 3 hrs by an audible alarm. Have IEC 61326-1 Electrical equipment for measurement, control and laboratory use -EMC requirements - Part 1: General requirements • Should Comply with the EMC requirements of the CE mark EMC Directive 2004/108/EC. | As per column no.2 |
145 | • Incubator should be compatible for both Pre Vacuum and Gravity Steam Sterilizers • Should have a built-in web app to allow create documentation that can be printed or saved electronically. • Equipment should show remaining minutes left of BI incubation. • Heating block temperature reading should be displayed • Positive BI Read-out time within 1 hr by an audible alarm. • Auto reader, self calibrating, to read Rapid Attest BI, with ten incubation wells • Compatible BI should be FDA cleared | As per column no.2 |
146 | • Chemical indicator tape to monitor Plasma sterilization by indicating a color change of blue to pink for easy identification of processed and unprocessed loads/ packs. •F or use in STERRAD® 100, 100S, NX® (Standard and Advanced cycles), 100NX® (Standard, Flex, Express and Duo cycles), AMSCO® V-PROâ„¢ 1 (Lumen cycle), AMSCO® V-PROâ„¢ 1 Plus (Lumen and Non Lumen cycles), and AMSCO® V-PROâ„¢ maX Low Temperature Sterilization System (Lumen, Non Lumen, and Flexible cycles) sterilizers. •Two year shelf life | As per column no.2 |
147 | • Process challenge device (PCD) that contains a 3-hour Readout Biological Indicator plus a Steam Chemical Integrator for Fast Turnaround Times for Load Releases • Class 5 Integrator Moving front Chemical integrators to verify all perimeters of steam sterilization together i.e. Time, Temperature and Quality of steam. Read out indicates Accept or Reject after processing. • Rapid BI Rapid readout biological indicators for steam sterilization containing a standardized, viable population of Bacillus stearothermophilus spores. The indicator detects the presence of viable spores by the production of fluorescence in one to three hours. Designed and certified as per ISO 11138 and EN 866. | As per column no.2 |
148 | • Test Packs for monitoring Vacuum formation in Autoclave chambers. • Test sheet along with penetration challenge material should be in a single easy handled pack. • Should be lead free • Weight per pack should be 110 to 125 gms • Early Warning Sheet indicates impending sterilizer failure earlier than the bowie dick test sheet | As per column no.2 |
149 | • Rapid readout biological indicators for steam sterilization containing a standardized, viable population of Bacillus stearothermophilus spores • The indicator detects the presence of viable spores within 1 hour in conjunction with Super Rapid Readout Incubator • Designed and certified as per ISO 11138 and EN 866. • Should be compatible with the pre Vacuum cycle of 132°C to 135°C, Should be compliant to ISO 11138-1:2006(en) Part 1 and ISO 11138-1:2006(en) Part 2 • Every box should contain Quality Assurance certificate with mention of Spore population, D- value & Z value • Should have a BSI Kitemark Certificate • Should have FDA clearance | As per column no.2 |
150 | • Moving front Chemical integrators, indicating Accept or Reject, to verify all perimeters of steam sterilization together i.e. Time, Temperature and Quality of steam. • Can be used for pack control monitoring of all 118-138ºC (245-280ºF) steam sterilization cycles Should be compliant to BS/ EN/ ISO 11140-1: 2005 • Should have 510 (k) registration • Should have a BSI Kitemark Certificate Pack of 500/box,2 box /case | As per column no.2 |
151 | The equipment must be a forced air warmer to deliver effective forced – air patient warming, It should be microprocessor based handy and with accurate temperature sensor system. Flicker-free operation defined as Meets IEC 61000-3-3 Standard, It should have audible and visual alarms in case of over temperature, It should have a washable protective hose cover, The equipment should be pole and bed mountable, Each equipment should be supplied with stand.Unit weight: 7KG, Airflow setting:2 speed, -adjustable Up to 44 CFM (20.8 L/s) | As per column no.2 |
152 | The equipment must be a forced air warmer to deliver effective forced – air patient warming, It should be microprocessor based handy and with accurate temperature sensor system. Flicker-free operation defined as Meets IEC 61000-3-3 Standard, It should have audible and visual alarms in case of over temperature, It should have a washable protective hose cover, The equipment should be pole and bed mountable, Each equipment should be supplied with stand.Unit weight: 4.5 KG, Airflow setting:One speed, non-adjustable Up to 44 CFM (20.8 L/s) | As per column no.2 |
153 | Full Body Blanket,Material that is soft, conformable, lightweight, and radiolucent,Uniform perforation pattern across the blanket surface ensures even convective warming,Non-inflated foot drapes guard against thermal injury to the heat-sensitive feet and lower legs,Patented blanket designs that provide even heat distribution Size 84 x 36 in (213 x 91 cm) | As per column no.2 |
154 | Pediatic full body blankes designed to bend in order to accommodate a wide range of surgical procedures and positions,soft, conformable, lightweight, and radiolucent,Non-inflated foot drapes guard against thermal injury to the heat- sensitive feet and lower legs and Patented blanket designs that provide even heat distribution Size 60 x 36 in (152 x 91 cm) | As per column no.2 |
155 | It is designed to bend in order to accommodate a wide range of surgical procedures and positions,Material that is soft, conformable, lightweight, and radiolucent and continuous adhesive strip to secures blanket to patient Size 60 x 36 in (152 x 91 cm) | As per column no.2 |
156 | Pediatric Long Blanket,Tube shape blanket which surrounds patient with warm air,It is designed to bend in order to accommodate a wide range of surgical procedures and positions.Size 74 x 8.5 in (188 x 21 cm) | As per column no.2 |
157 | It is designed to bend in order to accommodate a wide range of surgical procedures and positions,Material that is soft, conformable, lightweight, and radiolucent,Pass- through slit design allows for flexible patient positioning and accommodates the use of a drawsheet,Patented fluid outlets minimize pooling of fluids on the surface of the blanket Size 74 x 36 in (188 x 91 cm) | As per column no.2 |
158 | It is designed to bend in order to accommodate a wide range of surgical procedures and positions.two reselable hose ports and Patented fluid outlets minimize pooling of fluids on the surface of the blanket Size 60 x 32 in (152 x 81 cm) | As per column no.2 |
159 | It is designed to bend in order to accommodate a wide range of surgical procedures and positions,Should have integrated adhesive ,Foot Drape,and have large surgical access window Size 84 x 36 in (213 x 91 cm) | As per column no.2 |
160 | Lithotomy Underbody Blanket,Material that is soft, conformable, lightweight, and radiolucent,Advanced blanket designs warm the patient while providing full,Patented fluid outlets minimize pooling of fluids on the surface of the blanket unrestricted patient access64 x 36 in (160 x 91 cm) | As per column no.2 |
161 | Full Access Underbody Blanket ,Material that is soft, conformable, lightweight, and radiolucent,Advanced blanket designs warm the patient while providing full,Patented fluid outlets minimize pooling of fluids on the surface of the blanket unrestricted patient access,Size 84 x 36 in (221 x 91 cm) | As per column no.2 |
162 | Sterile Full Access Underbody Blanket,Material that is soft, conformable, lightweight, and radiolucent,Advanced blanket designs warm the patient while providing full,Patented fluid outlets minimize pooling of fluids on the surface of the blanket unrestricted patient access, Size 84 x 36 in (221 x 91 cm) | As per column no.2 |
163 | Multi Position Upperbody Blanket 622,Material that is soft, conformable, lightweight, and radiolucent,It is designed to bend in order to accommodate a wide range of surgical procedures and positions,Provides coverage for additional positions and accommodates a wider range of surgical procedures- supine, prone, and lateral, Beach chair, steep Trendelenburg (robotics), lithotomy, and plastic surgery position,Size 78 x 24 in (198 x 61 cm) | As per column no.2 |
164 | A non-invasive deep tissue body temperature monitoring sensor with a memory chip that facilitates a two hour continuous visual representation of the patient temperature trend on a control unit. The sensor should have a medical grade adhesive that is biocompatible with the human skin. Dimensions: 1.6inch diameter and 0.2 inches thickness. 25 units per case. Must be FDA CFG, ISO 13485, IEC and CE certified | As per column no.2 |
165 | A Non-invasive, temperature monitoring unit that can be used to continuously montior and record core temperature. The machine should have a memory display of at least 90 minutes. Weight of the control unit should be less than 150g and the length of the sensor cable should be over 350cm. | As per column no.2 |
166 | Silver impregnated foam dressing Size/Packing | As per column no.2 |
167 | Silver impregnated foam dressing Size/Packing: | As per column no.2 |
168 | Latex Free Polyester Cast Bandage is water activated | As per column no.2 |
169 | Latex Free Polyester Cast Bandage is water activated | As per column no.2 |
170 | Cotton and Viscose Pad, Binds Bacteria, Microbes,Pus and Debris. With DACC | As per column no.2 |
171 | Cotton and Viscose Pad, Binds Bacteria, Microbes,Pus and Debris. With DACC | As per column no.2 |
172 | Nano crystalline silver dressing made up of Rayon polyester | As per column no.2 |
173 | Nano crystalline silver dressing made up of Rayon polyester | As per column no.2 |
174 | Sterile Transparent Dressings for IV Lines | As per column no.2 |
175 | Sterile Transparent Dressings for IV Lines | As per column no.2 |
176 | Chlorohexidine Gauze Dressing | As per column no.2 |
177 | Electrochemically processed aqueous gel based solution with patented technology tolerance irrigation solution Strictly US-FDA approved .packaging = 60ML bottle gel | As per column no.2 |
178 | Electrochemically processed aqueous gel based solution with patented technology maximise tolerance irrigation solution Strictly US-FDA approved .packaging = 100 ML bottle gel | As per column no.2 |
179 | Electrochemically processed aqueous gel based solutionwith patented technology maximise tolerance irrigation solution Strictly US-FDA approved .packaging =120 ML bottle gel | As per column no.2 |
180 | Electrochemically processed aqueous gel based solution with patented technology maximise tolerance irrigation solution Strictly US-FDA approved .packaging = 200 ML JAR | As per column no.2 |
181 | Electrochemically processed aqueous gel based solution with patented technology maximise tolerance irrigation solution Strictly US-FDA approved .packaging = 400 ML JAR | As per column no.2 |
182 | Electrochemically processed aqueous based solution with microcyn technology patented: maximise tolerance irrigation solution.Strictly US-FDA approved packaging:- = 100ml bottle | As per column no.2 |
183 | Electrochemically processed aqueous based solution with patented technology maximise tolerance irrigation solution.Strictly US-FDA approved packaging = 500 ml | As per column no.2 |
184 | Electrochemically processed aqueous based solution with patented technology maximise tolerance irrigation solution. Strictly US-FDA approved Packaging:- = 1000 ml bottle (1 litre) | As per column no.2 |
185 | Electrochemically processed aqueous based solution with with patented technology for disinfectant maximise tolerance irrigation solution. Strictly US-FDA approved Packaging:- = 1000 ml bottle (1 litre) | As per column no.2 |
186 | Electrochemically processed aqueous based solution with patented technology ecosafe disinfectant maximise tolerance irrigation solution. Strictly US-FDA approved. Packaging :- = 5 litre jerricane | As per column no.2 |
187 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 5cm x 5Cm |
188 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 10cm x 10Cm |
189 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 10cm x 120Cm |
190 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 20cm x 40Cm |
191 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 40cm x 40Cm |
192 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 20cm x 20Cm |
193 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 4cm x 15Cm |
194 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 4cm x 25Cm |
195 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 4cm x 35Cm |
196 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 3 days. 10cm x 20Cm |
197 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 7 days. 5cm x 5Cm |
198 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 7 days. 15cm x 15Cm |
199 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 7 days. 10cm x 12.5Cm |
200 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 7 days. 20cm x 40Cm |
201 | Anti microbial silver dressing with flexible polyester mesh open weave structure | Antimicrobial barrier dressing with Silcryst Nanocrystals Silver consisting of low adherent wound contact layer of flexible and strectable polyester mesh with open weave structure coated with high density nanocrystalline silver effective against MRSA & VRE. which releases 70-100ppm of silver continuously for 7 days. 40cm x 40Cm |
202 | Iodine impregnated Theatre Incise Drape | A hygiene film coated with acrylic adhesive impregnated with PVP Iodine laminated with Silicon paper. Size 60cm x 35cm |
203 | Iodine impregnated Theatre Incise Drape | A hygiene film coated with acrylic adhesive impregnated with PVP Iodine laminated with Silicon paper. Size 65cm x 45cm |
204 | Iodine impregnated Theatre Incise Drape | A hygiene film coated with acrylic adhesive impregnated with PVP Iodine laminated with Silicon paper. Size 15cm x 10cm |
205 | Iodine impregnated Theatre Incise Drape | A hygiene film coated with acrylic adhesive impregnated with PVP Iodine laminated with Silicon paper. Size 30cm x 15cm |
206 | Iodine impregnated Theatre Incise Drape | A hygiene film coated with acrylic adhesive impregnated with PVP Iodine laminated with Silicon paper. Size 30cm x 30cm |
207 | Iodine impregnated Theatre Incise Drape | A hygiene film coated with acrylic adhesive impregnated with PVP Iodine laminated with Silicon paper. Size 65cm x 55cm |
208 | Iodine impregnated Theatre Incise Drape | A hygiene film coated with acrylic adhesive impregnated with PVP Iodine laminated with Silicon paper. Size 90cm x 45cm |
209 | Iodine impregnated Theatre Incise Drape | A hygiene film coated with acrylic adhesive impregnated with PVP Iodine laminated with Silicon paper. Size 90cm x 60cm |
210 | Antimicrobial Silver Dressing with nanocrystalline technology | AS ABOVE size: 5cmx5cm |
211 | Hydrocellular Foam Silicone Gel Adhesive Dressing10cmx20cm | An advanced triple-layer construction which combines an absorbent hydrocellular pad sandwiched between a perforated Soft Gel adhesive wound contact layer and a highly permeable waterproof outer film. Triple- action technology absorbs, retains, and transpires exudate to provide optimal fluid management. Maintains optimal moisture balance - Provides an optimal moist wound environment for the promotion of faster healing. Comes off lightly - Gentle adhesive allows less painful dressing changes Easier application - Gel adhesive holds the dressing in place 10 cm x 20cm, |
212 | Adhesive Zinc Tape 2.5cm x 10mtr Roll | As per colomn No.2 |
213 | Adhesive Zinc Tape 10cm x 10mtr Roll | As per colomn No.2 |
214 | Mobile and single use negative pressure wound therapy system | Mobile , portable and single use negative pressure wound therapy system without cannister .waterproof dressing pad with silicone adhesive contact layer and super absorbent crystals contained with fibers which can retain 300 ml fluid.Size: 25cmx25cm |
215 | Suction sickle knife | Curved, with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Cutting tissue) |
216 | Suction sickle knife | curved,leur lock,17cm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Acoustic Neuroma) |
217 | Suction dissector for ear drum | single curved right 3 mm, 13 cm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Preparation and aspiration of the cholesteatoma on the eardrum(protympanum |
218 | Suction dissector for ear drum | single curved left 3 mm, 13 cm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Preparation and aspiration of the cholesteatoma on the eardrum(protympanum) |
219 | Suction dissector for ear drum | Extra fine, right with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Preparation and aspiration of the cholesteatoma on the eardrum(protympanum) |
220 | Suction dissector for ear drum | Extra fine,left with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Preparation and aspiration of the cholesteatoma on the eardrum(protympanum) |
221 | Suction microhatches | 45° 2.0 mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For cutting the stapes joint and lifting the foot plate) |
222 | Suction micro hook | 45° 1.5 mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For cutting the stapes joint and lifting the foot plate) |
223 | Suction micro hook | 45° 1.0 mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For cutting the stapes joint and lifting the foot plate) |
224 | Preyer suction finder | dull (To examine antrum) |
225 | Suction round cut knife | Outside,2.5mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For removing the eardrum) |
226 | Suction round cut knife | Outside,2.0mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For removing the eardrum) |
227 | Suction round cut knife | Inside,2.5 mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent |
228 | Suction knife | Suction opening on right with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For removing the eardrum) |
229 | Suction knife | Suction opening on left with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (Ear canal section, preparation of meatal flap) |
230 | Suction dissector | dull,right angled with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent ( To remove the cholesteatoma) |
231 | Suction dissector | dull,left bent with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (To remove the cholesteatoma) |
232 | Suction dissector for attik | right side 6 mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For preparation and aspiration of cholesteatoma) |
233 | Suction dissector for attik | left side 6 mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For preparation and aspiration of cholesteatoma) |
234 | Suction dissector for sinus tympani | right side 6 mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Preparation and aspiration of the cholesteatoma in the hypotympanum) |
235 | Suction dissector for sinus tympani | left side 6 mm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Preparation and aspiration of the cholesteatoma in the hypotympanum) |
236 | Suction Curette | Curette with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For removal of bone structure) |
237 | Suction Curette | curved, leur lock,17cm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Acoustic Neuroma) |
238 | Suction dissector | right curved, leur lock,17cm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Acoustic Neuroma) |
239 | Suction dissector | left curved, leur lock,17cm with inbuilt controlled suction and 360 degree rotatable luer lock with 55 degree bent (For Acoustic Neuroma) |
240 | System Screen Basket for Panetti Instruments | with removable lid, 24x24x4.5 cm |
241 | Suction adapter | rotatable,55° bent, leur lock,male,hose attachment (Rotatable connecting element to the hose) |
242 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size:5x5 cm | As per colomn No.2 |
243 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size: 8x5 cm | As per colomn No.2 |
244 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size:8x8cm | As per colomn No.2 |
245 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size: 10x10cm | As per colomn No.2 |
246 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size: 8*8*1cm | As per colomn No.2 |
247 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size:S5*5 cm | As per colomn No.2 |
248 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size: 5x5x1cm | As per colomn No.2 |
249 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size: 3.5X3.5x1cm | As per colomn No.2 |
250 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size:1x4cm | As per colomn No.2 |
251 | Haemostatic Dressing in Sponge/Pad form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof packing. Manufactured in India, GMP & ISO 13485. Certified by European CE Mark / USFDA Size:1x8cm | As per colomn No.2 |
252 | Advance wound dressing Non Woven Highly absorbent, haemostatic gelling fibre composed of 100% Natural Biopolymer with a net positive charge, Gamma sterilised & moisture proof packing. Manufactured in India GMP & ISO 13485 certified. Size:10x10cm | As per colomn No.2 |
253 | Advance wound dressing Non Woven Highly absorbent, haemostatic gelling fibre composed of 100% Natural Biopolymer with a net positive charge, Gamma sterilised & moisture proof packing. Manufactured in India GMP & ISO 13485 certified. Size: 10x5cm | As per colomn No.2 |
254 | Advance wound dressing Non Woven Highly absorbent, haemostatic gelling fibre composed of 100% Natural Biopolymer with a net positive charge, Gamma sterilised & moisture proof packing. Manufactured in India GMP & ISO 13485 certified. Size: 2.5X30cm | As per colomn No.2 |
255 | Advance wound dressing Non Woven Highly absorbent, haemostatic gelling fibre composed of 100% Natural Biopolymer with a net positive charge, Gamma sterilised & moisture proof packing. Manufactured in India GMP & ISO 13485 certified. Size: 15x15cm | As per colomn No.2 |
256 | Advance wound dressing Non Woven Highly absorbent, haemostatic gelling fibre composed of 100% Natural Biopolymer with a net positive charge, Gamma sterilised & moisture proof packing. Manufactured in India GMP & ISO 13485 certified. Size: 20x30cm | As per colomn No.2 |
257 | Advance wound dressing Non Woven Highly absorbent, haemostatic gelling fibre composed of 100% Natural Biopolymer with a net positive charge, Gamma sterilised & moisture proof packing. Manufactured in India GMP & ISO 13485 certified. Size: 45x45cm | As per colomn No.2 |
258 | Haemostatic dressing Highly Absorbent in Z- Fold form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof Vacuum packing. Manufactured in India, GMP & ISO 13485. Certified European CE Mark. Rolled Gauze Size: 7.6 cm x 50 cm | As per colomn No.2 |
259 | Haemostatic dressing Highly Absorbent in Z- Fold form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof Vacuum packing. Manufactured in India, GMP & ISO 13485. Certified European CE Mark. Rolled Gauze Size: 7.6 cm x 100 cm | As per colomn No.2 |
260 | Haemostatic dressing Highly Absorbent in Z- Fold form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof Vacuum packing. Manufactured in India, GMP & ISO 13485. Certified European CE Mark. Rolled Gauze Size: 7.6 cm x 150cm | As per colomn No.2 |
261 | Haemostatic dressing Highly Absorbent in Z- Fold form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof Vacuum packing. Manufactured in India, GMP & ISO 13485. Certified European CE Mark. Rolled Gauze Size: 7.6*300 cm | As per colomn No.2 |
262 | Haemostatic dressing Highly Absorbent in Z- Fold form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof Vacuum packing. Manufactured in India, GMP & ISO 13485. Certified European CE Mark. Z-fold Size: 7.6*100 cm | As per colomn No.2 |
263 | Haemostatic dressing Highly Absorbent in Z- Fold form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof Vacuum packing. Manufactured in India, GMP & ISO 13485. Certified European CE Mark. Z-fold Size: 7.6*150 cm | As per colomn No.2 |
264 | Haemostatic dressing Highly Absorbent in Z- Fold form made of 100% Natural Biopolymer with a Net Positive Charge, Gamma Sterilized & Moisture proof Vacuum packing. Manufactured in India, GMP & ISO 13485. Certified European CE Mark. Z-fold Size: 7.6*300 cm | As per colomn No.2 |
265 | Electrochemically solution with Hypochrous acid and sodium hyochloride solution with neutral PH non toxic Human skin friendly and wound irrigation size-500 ml | As per colomn No.2 |
266 | Electrochemically solution with Hypochrous acid and sodium hyochloride solution with neutral PH non toxic Human skin friendly and wound irrigation size-1000 ml | As per colomn No.2 |
267 | DISPOSABLE BLADE FOR Mcgrath VIDEO ALRYNGOSCOPE | Blade should be disposable , Blade should be suited for Mcgrath Video Laryngoscope, Size range : 1, 2, 3, 4, Special size for difficult intubation : Size X, Blade material should be Fog - Free medical grade polymer |
268 | Battery For Mcgrath Video Laryngoscope | Battery Should be Lithium, Battery should have 3.6V, Battery shuld be suited for Mcgrath Video Laryngoscope |
269 | Reusable Nellcor Covidien spo2 sensor Adult (DS100A) for Nellcor Pulse oximeter | Sensor should be Reusable, Patient type : Adult, Sensor should be original Nellcor Covidien, Sensor should be suited for Nellcor covidien pulse oximeter |
270 | Reusable Nellcor Covidien spo2 sensor Neonatal (DY-S) for Nellcor Pulse oximeter | Sensor should be Reusable, Patient type : NEONATAL, Sensor should be original Nellcor Covidien, Sensor should be suited for Nellcor covidien pulse oximeter |
271 | Reusable Nellcor Covidien spo2 sensor PEDIATRIC (FLEXMAX-P) for Nellcor Pulse oximeter | Sensor should be Reusable, Patient type : PEDIATRIC, Sensor should be from silicon, Sensor should be original Nellcor Covidien, Sensor should be suited for Nellcor covidien pulse oximeter |
272 | Disposable Nellcor Covidien spo2 sensor for neonatal for Nellcor Pulse oximeter | Sensor shuld be original nellcor covidien, Sensor shuold be suited for nellcor covidien pulse oximeter, Sensor should be Disoapoble, Technolgy : Oximax, Patient type : Ne, Sensor shuold be soft for fragile skinonatal /pediatric, Sensor should be non adhesive |
273 | BIS SENSOR -QUOTRO | Sensor should be 4 electrode, Sensor should be suitable for Covidien Bis Monitor, Sensor should be LATEX Free, Sensor should be disposable, Peel-¬and- ¬stick simplicity |
274 | Disposable Blanket For Covidien Patient warmer | Blanket should be Disposable, Blanket should be Suited for Covidien Warm touch Patient warmer, size : Full Body, Upper Body , Lower body, Pediatric, Should be latex free, The blanket is soft and flexible to permit custom draping for almost any procedure, Quick-connect reduces the risk of tearing the blanket when the hose nozzle is inserted., Quilted construction prevents billowing, promotes uniform airflow and helps the blanket conform to the patients body. |
275 | Disposable Sampling line for Micro stream Capnograph | Sampling line should be disposable, Should be suitable for Medtronic Micro stream Capnograph, Should available in range of : Intubated & Non Intubated separate, Integrated, single-piece airway gas sampling lines comprised of the patient cannula or airway adapter, water trap and a sterilizing grade filter that is designed to reduce the risk of biohazard contamination of the patient monitor., Uni-junctionâ„¢ technology is designed to ensure proper sampling for patients who alternate between oral and nasal breathing.F88, Should have Integrated nepheon filter |
276 | Pediatric - Airway Balloon Catheter- 5mm x 24mm | • It should have a non- compliant Balloon with puncture resistance, the design maintains consistent diameter through multiple dilations. • It should have a working length of 42.5 CMS. • It should have a flexible shaft with stylet optimised for airway anatomy. • Airway Balloons should have atraumatic balloon & stylet tip to crosses narrow stenosis. • Airway Balloon should have stylet to help enhanced support & manoeuvrability. • Airway Balloon should have malleable shaft can be custom – shaped for easy access & direct visualization. • Airway Balloon should reach its stated size at minimum of 12 atm to 16 atm and should withstand 17 atm pressures as per sizes of the Airway balloons. • Balloon Catheter should be approved by credible authorities for further safety of patients. |
277 | Pediatric - Airway Balloon Catheter- 7mm x 24mm | • It should have a non- compliant Balloon with puncture resistance, the design maintains consistent diameter through multiple dilations. • It should have a working length of 42.5 CMS. • It should have a flexible shaft with stylet optimised for airway anatomy. • Airway Balloons should have atraumatic balloon & stylet tip to crosses narrow stenosis. • Airway Balloon should have stylet to help enhanced support & manoeuvrability. • Airway Balloon should have malleable shaft can be custom – shaped for easy access & direct visualization. • Airway Balloon should reach its stated size at minimum of 12 atm to 16 atm and should withstand 17 atm pressures as per sizes of the Airway balloons. • Balloon Catheter should be approved by credible authorities for further safety of patients. |
278 | Pediatric - Airway Balloon Catheter- 9mm x 24mm | • It should have a non- compliant Balloon with puncture resistance, the design maintains consistent diameter through multiple dilations. • It should have a working length of 42.5 CMS. • It should have a flexible shaft with stylet optimised for airway anatomy. • Airway Balloons should have atraumatic balloon & stylet tip to crosses narrow stenosis. • Airway Balloon should have stylet to help enhanced support & manoeuvrability. • Airway Balloon should have malleable shaft can be custom – shaped for easy access & direct visualization. • Airway Balloon should reach its stated size at minimum of 12 atm to 16 atm and should withstand 17 atm pressures as per sizes of the Airway balloons. • Balloon Catheter should be approved by credible authorities for further safety of patients. |
279 | Adult - Airway Balloon Catheter-10mm x 40mm | • It should have a non- compliant Balloon with puncture resistance, the design maintains consistent diameter through multiple dilations. • It should have a working length of 42.5 CMS. • It should have a flexible shaft with stylet optimised for airway anatomy. • Airway Balloons should have atraumatic balloon & stylet tip to crosses narrow stenosis. • Airway Balloon should have stylet to help enhanced support & manoeuvrability. • Airway Balloon should have malleable shaft can be custom – shaped for easy access & direct visualization. • Airway Balloon should reach its stated size at minimum 12 atm to 16 atm and should withstand 17 atm pressures as per sizes of the Airway balloons. • Balloon Catheter should be approved by credible authorities for further safety of patients |
280 | Adult - Airway Balloon Catheter-12mm x 40mm | • It should have a non- compliant Balloon with puncture resistance, the design maintains consistent diameter through multiple dilations. • It should have a working length of 42.5 CMS. • It should have a flexible shaft with stylet optimised for airway anatomy. • Airway Balloons should have atraumatic balloon & stylet tip to crosses narrow stenosis. • Airway Balloon should have stylet to help enhanced support & manoeuvrability. • Airway Balloon should have malleable shaft can be custom – shaped for easy access & direct visualization. • Airway Balloon should reach its stated size at minimum 12 atm to 16 atm and should withstand 17 atm pressures as per sizes of the Airway balloons. • Balloon Catheter should be approved by credible authorities for further safety of patients |
281 | Adult - Airway Balloon Catheter-14mm x 40mm | • It should have a non- compliant Balloon with puncture resistance, the design maintains consistent diameter through multiple dilations. • It should have a working length of 42.5 CMS. • It should have a flexible shaft with stylet optimised for airway anatomy. • Airway Balloons should have atraumatic balloon & stylet tip to crosses narrow stenosis. • Airway Balloon should have stylet to help enhanced support & manoeuvrability. • Airway Balloon should have malleable shaft can be custom – shaped for easy access & direct visualization. • Airway Balloon should reach its stated size at minimum 12 atm to 16 atm and should withstand 17 atm pressures as per sizes of the Airway balloons. • Balloon Catheter should be approved by credible authorities for further safety of patients |
282 | Adult - Airway Balloon Catheter-16mm x 40mm | • It should have a non- compliant Balloon with puncture resistance, the design maintains consistent diameter through multiple dilations. • It should have a working length of 42.5 CMS. • It should have a flexible shaft with stylet optimised for airway anatomy. • Airway Balloons should have atraumatic balloon & stylet tip to crosses narrow stenosis. • Airway Balloon should have stylet to help enhanced support & manoeuvrability. • Airway Balloon should have malleable shaft can be custom – shaped for easy access & direct visualization. • Airway Balloon should reach its stated size at minimum 12 atm to 16 atm and should withstand 17 atm pressures as per sizes of the Airway balloons. • Balloon Catheter should be approved by credible authorities for further safety of patients |
283 | Balloon inflation device – Inflation Device. | • It should have an ergonomic piston handle for safe and controlled inflation/deflation of Airway balloon catheter. • It should have clear grading of different pressure levels. • It should have high pressure connector tubing to connect to the balloon catheter. • It should be compatible with different Airway balloon catheters. • It should have clear high pressure cylinder barrel to indicate the level of saline/ fluid inside the inflation device. • It should have a piston locking system to prevent accidental inflation/deflation of the Airway balloon catheter. • It should be approved by credible authorities for further safety of patients. |
284 | Lumbo Sacral Belt(US FDA Certified – Registration No -):- Should be made from extra strong highly porous orthopaedic webbing containing heat resistant rubber & having high modulus of elasticity. Should have ALLIGATOR TABS at the edge of the hook loop closures for nice holding grip &aesthetics. Should have ANTI SKID holder strap for easy closure of the belt. Tough & Flexi Nylon Bars & Polypropylene Strips should be provided at the back for good immobilisation. Double pull elastic mechanism for firm grip & extra compression to the L.S region. Sizing should be S = 28†- 34†(Small) | As per colomn No.2 |
285 | Lumbo Sacral Belt(US FDA Certified – Registration No -):- Should be made from extra strong highly porous orthopaedic webbing containing heat resistant rubber & having high modulus of elasticity. Should have ALLIGATOR TABS at the edge of the hook loop closures for nice holding grip &aesthetics. Should have ANTI SKID holder strap for easy closure of the belt. Tough & Flexi Nylon Bars & Polypropylene Strips should be provided at the back for good immobilisation. Double pull elastic mechanism for firm grip & extra compression to the L.S region. Sizing should be M = 34†- 40†(Medium) | As per colomn No.2 |
286 | Lumbo Sacral Belt(US FDA Certified – Registration No -):- Should be made from extra strong highly porous orthopaedic webbing containing heat resistant rubber & having high modulus of elasticity. Should have ALLIGATOR TABS at the edge of the hook loop closures for nice holding grip &aesthetics. Should have ANTI SKID holder strap for easy closure of the belt. Tough & Flexi Nylon Bars & Polypropylene Strips should be provided at the back for good immobilisation. Double pull elastic mechanism for firm grip & extra compression to the L.S region. Sizing should be L = 40†- 46†(Large) | As per colomn No.2 |
287 | Lumbo Sacral Belt(US FDA Certified – Registration No -):- Should be made from extra strong highly porous orthopaedic webbing containing heat resistant rubber & having high modulus of elasticity. Should have ALLIGATOR TABS at the edge of the hook loop closures for nice holding grip &aesthetics. Should have ANTI SKID holder strap for easy closure of the belt. Tough & Flexi Nylon Bars & Polypropylene Strips should be provided at the back for good immobilisation. Double pull elastic mechanism for firm grip & extra compression to the L.S region. Sizing should be XL = 46†- 52†(XL) | As per colomn No.2 |
288 | Lumbo Sacral Belt(US FDA Certified – Registration No -):- Should be made from extra strong highly porous orthopaedic webbing containing heat resistant rubber & having high modulus of elasticity. Should have ALLIGATOR TABS at the edge of the hook loop closures for nice holding grip &aesthetics. Should have ANTI SKID holder strap for easy closure of the belt. Tough & Flexi Nylon Bars & Polypropylene Strips should be provided at the back for good immobilisation. Double pull elastic mechanism for firm grip & extra compression to the L.S region. Sizing should be XXL = 52†- 58â€. (XXL) | As per colomn No.2 |
289 | Contoured L.S.Support (US FDA Certified – Registration No -):- Should be made from extra strong Orthopaedic webbing containing Heat Resistant Rubber. The malleable light weight Aluminium back splints should be contoured to ensure effective immobilisation, correct posture & should be customizable for accurate shape & enhanced immobilisation. Should have Double Pull Elastic Mechanism for firm grip & extra compression to the L.S.region. Sizing should be S = 28†- 34†(Small) | As per colomn No.2 |
290 | Contoured L.S.Support (US FDA Certified – Registration No -):- Should be made from extra strong Orthopaedic webbing containing Heat Resistant Rubber. The malleable light weight Aluminium back splints should be contoured to ensure effective immobilisation, correct posture & should be customizable for accurate shape & enhanced immobilisation. Should have Double Pull Elastic Mechanism for firm grip & extra compression to the L.S.region. Sizing should be M = 34†- 40â€, (Medium) | As per colomn No.2 |
291 | Contoured L.S.Support (US FDA Certified – Registration No -):- Should be made from extra strong Orthopaedic webbing containing Heat Resistant Rubber. The malleable light weight Aluminium back splints should be contoured to ensure effective immobilisation, correct posture & should be customizable for accurate shape & enhanced immobilisation. Should have Double Pull Elastic Mechanism for firm grip & extra compression to the L.S.region. Sizing should be L = 40†- 46â€, (Large) | As per colomn No.2 |
292 | Contoured L.S.Support (US FDA Certified – Registration No -):- Should be made from extra strong Orthopaedic webbing containing Heat Resistant Rubber. The malleable light weight Aluminium back splints should be contoured to ensure effective immobilisation, correct posture & should be customizable for accurate shape & enhanced immobilisation. Should have Double Pull Elastic Mechanism for firm grip & extra compression to the L.S.region. Sizing should be XL = 46†- 52†(XL) | As per colomn No.2 |
293 | Contoured L.S.Support (US FDA Certified – Registration No -):- Should be made from extra strong Orthopaedic webbing containing Heat Resistant Rubber. The malleable light weight Aluminium back splints should be contoured to ensure effective immobilisation, correct posture & should be customizable for accurate shape & enhanced immobilisation. Should have Double Pull Elastic Mechanism for firm grip & extra compression to the L.S.region. Sizing should be XXL = 52†- 58â€. (XXL) | As per colomn No.2 |
294 | LumboLacepull Brace ( US FDA Certified – Registration No -):- Should be made from very high quality ventilated fabric with TWO WAY lacepull mechanism to provide multiplying effect. Should elongate the thoracic cavity & thereby decompress the IVD’s. Anatomic back panel to provide an excellent fitting rigid immobilisation & excellent fitting. Should have a front panel to house the rigid back panel for enhanced decompression of the IVD’s. [Universal (28†- 44â€) AND Special (44†- 52â€)] | As per colomn No.2 |
295 | Rib Belt (US FDA Certified – Registration No -):- Should be made from exxtra strong Orthopaedic webbing & extra porous material to ensure adequate compression, good immobilisation & patient comfort. Should be able to compress & hold the incision during coughing bouts & alleviate pain. Additional ETHAFOAM PAD to be provided for strong localized grip at the fracture site so as to ensure improved immobilisation & healing. (Small) | As per colomn No.2 |
296 | Rib Belt (US FDA Certified – Registration No -):- Should be made from exxtra strong Orthopaedic webbing & extra porous material to ensure adequate compression, good immobilisation & patient comfort. Should be able to compress & hold the incision during coughing bouts & alleviate pain. Additional ETHAFOAM PAD to be provided for strong localized grip at the fracture site so as to ensure improved immobilisation & healing. (Medium) | As per colomn No.2 |
297 | Rib Belt (US FDA Certified – Registration No -):- Should be made from exxtra strong Orthopaedic webbing & extra porous material to ensure adequate compression, good immobilisation & patient comfort. Should be able to compress & hold the incision during coughing bouts & alleviate pain. Additional ETHAFOAM PAD to be provided for strong localized grip at the fracture site so as to ensure improved immobilisation & healing. (Large) | As per colomn No.2 |
298 | Rib Belt (US FDA Certified – Registration No -):- Should be made from exxtra strong Orthopaedic webbing & extra porous material to ensure adequate compression, good immobilisation & patient comfort. Should be able to compress & hold the incision during coughing bouts & alleviate pain. Additional ETHAFOAM PAD to be provided for strong localized grip at the fracture site so as to ensure improved immobilisation & healing. (XL) | As per colomn No.2 |
299 | Taylor’s Brace URBANE (US FDA Certified – Registraion No -):- Should be made from a very light weight triple layered fabric with a system of INTERCONNECTED HOLES for excellent ventilation& patient comfort. Light weight Spinal braces to provide full support & comprehensive coverage to thoraco – lumbar – sacrum spinal section. Immobilisation of the spine should be achieved in Neutral position with 2 rigid para spinal bars which prevent both flexion & hyperextension. Thoracic horizontal splints to prevent rotation of upper torso & pelvic splints to envelope the pelvis for rigid immobilisation of the entire vertebral column. (Universal short, Universal long, Special short,Special long) | As per colomn No.2 |
300 | Collar Soft Firm Density (US FDA Certified – Registration No -):- Should be made from very high density PU foam and have an anatomic design to enure uniform support, better immobilisation& quick relief. Should have a perforated collar body &hypoallergnic cotton stockinet for improved venilation, comfort & compliance. Should have long hook loop tape to ensure snug fitting & easy application (Small) | As per colomn No.2 |
301 | Collar Soft Firm Density (US FDA Certified – Registration No -):- Should be made from very high density PU foam and have an anatomic design to enure uniform support, better immobilisation& quick relief. Should have a perforated collar body &hypoallergnic cotton stockinet for improved venilation, comfort & compliance. Should have long hook loop tape to ensure snug fitting & easy application (Medium) | As per colomn No.2 |
302 | Collar Soft Firm Density (US FDA Certified – Registration No -):- Should be made from very high density PU foam and have an anatomic design to enure uniform support, better immobilisation& quick relief. Should have a perforated collar body &hypoallergnic cotton stockinet for improved venilation, comfort & compliance. Should have long hook loop tape to ensure snug fitting & easy application (Large) | As per colomn No.2 |
303 | Collar Soft Firm Density (US FDA Certified – Registration No -):- Should be made from very high density PU foam and have an anatomic design to enure uniform support, better immobilisation& quick relief. Should have a perforated collar body &hypoallergnic cotton stockinet for improved venilation, comfort & compliance. Should have long hook loop tape to ensure snug fitting & easy application (XL) | As per colomn No.2 |
304 | Cervical Collar Soft with Support (US FDA Certified – Registration No -):-Should be made from high density PU Foam for improved support, cushioning & long functional life. Should be HYPOALLERGENIC with high GSM cotton stockinet for improved comfort. The LDPE sheet should be thick with ROUNDED EDGES to ensure rigid immobilisation without a bite. The YELETS provided for improved ventilation & comfort should be RUST PROOF. (Small) | As per colomn No.2 |
305 | Cervical Collar Soft with Support (US FDA Certified – Registration No -):-Should be made from high density PU Foam for improved support, cushioning & long functional life. Should be HYPOALLERGENIC with high GSM cotton stockinet for improved comfort. The LDPE sheet should be thick with ROUNDED EDGES to ensure rigid immobilisation without a bite. The YELETS provided for improved ventilation & comfort should be RUST PROOF. (Medium) | As per colomn No.2 |
306 | Cervical Collar Soft with Support (US FDA Certified – Registration No -):-Should be made from high density PU Foam for improved support, cushioning & long functional life. Should be HYPOALLERGENIC with high GSM cotton stockinet for improved comfort. The LDPE sheet should be thick with ROUNDED EDGES to ensure rigid immobilisation without a bite. The YELETS provided for improved ventilation & comfort should be RUST PROOF. (Large) | As per colomn No.2 |
307 | Cervical Collar Soft with Support (US FDA Certified – Registration No -):-Should be made from high density PU Foam for improved support, cushioning & long functional life. Should be HYPOALLERGENIC with high GSM cotton stockinet for improved comfort. The LDPE sheet should be thick with ROUNDED EDGES to ensure rigid immobilisation without a bite. The YELETS provided for improved ventilation & comfort should be RUST PROOF. (XL) | As per colomn No.2 |
308 | Cervical Orthosis PLASTAZOTE (US FDA Certified – Registration No -):-Should be made from eco friendly, durable, hypoallergenic, lightweight &eay to clean PLASTAZOTE material. Should hav a frontal opening toallow use of Tracheostomy tube. It should be a 2 piece anatomical design to improve immobilisation, comfort & ease of application. (CH) | As per colomn No.2 |
309 | Cervical Orthosis PLASTAZOTE (US FDA Certified – Registration No -):-Should be made from eco friendly, durable, hypoallergenic, lightweight &eay to clean PLASTAZOTE material. Should hav a frontal opening toallow use of Tracheostomy tube. It should be a 2 piece anatomical design to improve immobilisation, comfort & ease of application. (Small) | As per colomn No.2 |
310 | Cervical Orthosis PLASTAZOTE (US FDA Certified – Registration No -):-Should be made from eco friendly, durable, hypoallergenic, lightweight &eay to clean PLASTAZOTE material. Should hav a frontal opening toallow use of Tracheostomy tube. It should be a 2 piece anatomical design to improve immobilisation, comfort & ease of application. (Medium) | As per colomn No.2 |
311 | Cervical Orthosis PLASTAZOTE (US FDA Certified – Registration No -):-Should be made from eco friendly, durable, hypoallergenic, lightweight &eay to clean PLASTAZOTE material. Should hav a frontal opening toallow use of Tracheostomy tube. It should be a 2 piece anatomical design to improve immobilisation, comfort & ease of application. (Large) | As per colomn No.2 |
312 | Cervical Orthosis PLASTAZOTE (US FDA Certified – Registration No -):-Should be made from eco friendly, durable, hypoallergenic, lightweight &eay to clean PLASTAZOTE material. Should hav a frontal opening toallow use of Tracheostomy tube. It should be a 2 piece anatomical design to improve immobilisation, comfort & ease of application. (XL) | As per colomn No.2 |
313 | Universal Shoulder Immobiliser (US FDA Certified – Registration No -):- Should be made from 3 layered PUF fused fabric for durability, soft feel, plush looks & wrinkle free property. Should be a 2 piece design with the pouch offering a proper support, correct posture, higher immobilisation & easy application. Should have an Arm Restraint Band for additional locking & enhanced immbilisation of the arm & shoulder. Should have double sraps at the shoulder so that the load is divided uniformly & improves comfort. (Universal / Special) | As per colomn No.2 |
314 | Elastic Shoulder Immobiliser (US FDA Certified – Registration No -):- Should have a scientific design providing 6 way immobilisation, proper ventilation, comfort and be able to be used in patients confined to bed OR with open shoulder wounds. Should have additional shoulder cups for improv immobilisation, grip on injured shoulder & enhance patient confidence. (Small) | As per colomn No.2 |
315 | Elastic Shoulder Immobiliser (US FDA Certified – Registration No -):- Should have a scientific design providing 6 way immobilisation, proper ventilation, comfort and be able to be used in patients confined to bed OR with open shoulder wounds. Should have additional shoulder cups for improv immobilisation, grip on injured shoulder & enhance patient confidence. (Medium) | As per colomn No.2 |
316 | Elastic Shoulder Immobiliser (US FDA Certified – Registration No -):- Should have a scientific design providing 6 way immobilisation, proper ventilation, comfort and be able to be used in patients confined to bed OR with open shoulder wounds. Should have additional shoulder cups for improv immobilisation, grip on injured shoulder & enhance patient confidence. (Large) | As per colomn No.2 |
317 | Elastic Shoulder Immobiliser (US FDA Certified – Registration No -):- Should have a scientific design providing 6 way immobilisation, proper ventilation, comfort and be able to be used in patients confined to bed OR with open shoulder wounds. Should have additional shoulder cups for improv immobilisation, grip on injured shoulder & enhance patient confidence. (XL) | As per colomn No.2 |
318 | Elastic Shoulder Immobiliser (US FDA Certified – Registration No -):- Should have a scientific design providing 6 way immobilisation, proper ventilation, comfort and be able to be used in patients confined to bed OR with open shoulder wounds. Should have additional shoulder cups for improv immobilisation, grip on injured shoulder & enhance patient confidence. (XXL) | As per colomn No.2 |
319 | Clavicle Brace Velcro (US FDA Certified – Registration No -):- Reverse buckle fastening with hook loop tapes to offer better tightening & grip and PU foam padding to ensure no underarm rashes. Figure of 8 design with lateral vctor for ensuring linear union of the bone, easy application & tightening of the braace. (CH) | As per colomn No.2 |
320 | Clavicle Brace Velcro (US FDA Certified – Registration No -):- Reverse buckle fastening with hook loop tapes to offer better tightening & grip and PU foam padding to ensure no underarm rashes. Figure of 8 design with lateral vctor for ensuring linear union of the bone, easy application & tightening of the braace. (Small) | As per colomn No.2 |
321 | Clavicle Brace Velcro (US FDA Certified – Registration No -):- Reverse buckle fastening with hook loop tapes to offer better tightening & grip and PU foam padding to ensure no underarm rashes. Figure of 8 design with lateral vctor for ensuring linear union of the bone, easy application & tightening of the braace. (Medium) | As per colomn No.2 |
322 | Clavicle Brace Velcro (US FDA Certified – Registration No -):- Reverse buckle fastening with hook loop tapes to offer better tightening & grip and PU foam padding to ensure no underarm rashes. Figure of 8 design with lateral vctor for ensuring linear union of the bone, easy application & tightening of the braace. (Large) | As per colomn No.2 |
323 | Clavicle Brace Velcro (US FDA Certified – Registration No -):- Reverse buckle fastening with hook loop tapes to offer better tightening & grip and PU foam padding to ensure no underarm rashes. Figure of 8 design with lateral vctor for ensuring linear union of the bone, easy application & tightening of the braace. (XL) | As per colomn No.2 |
324 | Clavicle Brace Velcro (US FDA Certified – Registration No -):- Reverse buckle fastening with hook loop tapes to offer better tightening & grip and PU foam padding to ensure no underarm rashes. Figure of 8 design with lateral vctor for ensuring linear union of the bone, easy application & tightening of the braace. (XXL) | As per colomn No.2 |
325 | Pouch Arm Sling Baggy (US FDA Certified – Registration No -):- Shoul be made from 3 layered PU bonded fabric for better durability, soft feel & wrinkle free property. The design should ensure maximum support & coverage of the arm and be able to accomodate bulky casts/bandges. Should have a THUMB CRADLE to reduce thumb fatigue and an adjustable ETHAFOAM shoulder pd to take the load& improve comfort. Adjustable sling should optimise positioning of the arm. (CH) | As per colomn No.2 |
326 | Pouch Arm Sling Baggy (US FDA Certified – Registration No -):- Shoul be made from 3 layered PU bonded fabric for better durability, soft feel & wrinkle free property. The design should ensure maximum support & coverage of the arm and be able to accomodate bulky casts/bandges. Should have a THUMB CRADLE to reduce thumb fatigue and an adjustable ETHAFOAM shoulder pd to take the load& improve comfort. Adjustable sling should optimise positioning of the arm. (Small) | As per colomn No.2 |
327 | Pouch Arm Sling Baggy (US FDA Certified – Registration No -):- Shoul be made from 3 layered PU bonded fabric for better durability, soft feel & wrinkle free property. The design should ensure maximum support & coverage of the arm and be able to accomodate bulky casts/bandges. Should have a THUMB CRADLE to reduce thumb fatigue and an adjustable ETHAFOAM shoulder pd to take the load& improve comfort. Adjustable sling should optimise positioning of the arm. (Medium) | As per colomn No.2 |
328 | Pouch Arm Sling Baggy (US FDA Certified – Registration No -):- Shoul be made from 3 layered PU bonded fabric for better durability, soft feel & wrinkle free property. The design should ensure maximum support & coverage of the arm and be able to accomodate bulky casts/bandges. Should have a THUMB CRADLE to reduce thumb fatigue and an adjustable ETHAFOAM shoulder pd to take the load& improve comfort. Adjustable sling should optimise positioning of the arm. (Large) | As per colomn No.2 |
329 | Pouch Arm Sling Baggy (US FDA Certified – Registration No -):- Shoul be made from 3 layered PU bonded fabric for better durability, soft feel & wrinkle free property. The design should ensure maximum support & coverage of the arm and be able to accomodate bulky casts/bandges. Should have a THUMB CRADLE to reduce thumb fatigue and an adjustable ETHAFOAM shoulder pd to take the load& improve comfort. Adjustable sling should optimise positioning of the arm. (XL) | As per colomn No.2 |
330 | Pouch Arm Sling Baggy (US FDA Certified – Registration No -):- Shoul be made from 3 layered PU bonded fabric for better durability, soft feel & wrinkle free property. The design should ensure maximum support & coverage of the arm and be able to accomodate bulky casts/bandges. Should have a THUMB CRADLE to reduce thumb fatigue and an adjustable ETHAFOAM shoulder pd to take the load& improve comfort. Adjustable sling should optimise positioning of the arm. (XXL) | As per colomn No.2 |
331 | Cast Shoe Rocker Sole (US FDA Certified – Registration No -):- Should be VERY LIGHT WEIGHTwiht strong & durable upper to protect the cast from getting soiled OR mechanicaal damage. Should have a quick drying material wih enhanced aesthetics. The ROCKER SOLE is to ensure that the user does not have a FLAT FOOTING on the proximal OR distal axis of the feet so as to enhance the balance, restore normal Gait & early Ambulation. (Small) | As per colomn No.2 |
332 | Cast Shoe Rocker Sole (US FDA Certified – Registration No -):- Should be VERY LIGHT WEIGHTwiht strong & durable upper to protect the cast from getting soiled OR mechanicaal damage. Should have a quick drying material wih enhanced aesthetics. The ROCKER SOLE is to ensure that the user does not have a FLAT FOOTING on the proximal OR distal axis of the feet so as to enhance the balance, restore normal Gait & early Ambulation. (Medium) | As per colomn No.2 |
333 | Cast Shoe Rocker Sole (US FDA Certified – Registration No -):- Should be VERY LIGHT WEIGHTwiht strong & durable upper to protect the cast from getting soiled OR mechanicaal damage. Should have a quick drying material wih enhanced aesthetics. The ROCKER SOLE is to ensure that the user does not have a FLAT FOOTING on the proximal OR distal axis of the feet so as to enhance the balance, restore normal Gait & early Ambulation. (Large) | As per colomn No.2 |
334 | Cast Shoe Rocker Sole (US FDA Certified – Registration No -):- Should be VERY LIGHT WEIGHTwiht strong & durable upper to protect the cast from getting soiled OR mechanicaal damage. Should have a quick drying material wih enhanced aesthetics. The ROCKER SOLE is to ensure that the user does not have a FLAT FOOTING on the proximal OR distal axis of the feet so as to enhance the balance, restore normal Gait & early Ambulation. (XL) | As per colomn No.2 |
335 | Pouch Arm Sling Urbane (US FDA Certified – Registration No -):- Should be made fom triple layered light weight fabric with a well ventilated system of interconnected holes. Should accomodate bulky casts and provide maximum support to the injured arm. Should have super soft cushion adjustable pad to ensure a very high level of comfort & least pressure on the shoulders. Y clamp hook fasteners to ensure customized sizing of the sling (Small) | As per colomn No.2 |
336 | Pouch Arm Sling Urbane (US FDA Certified – Registration No -):- Should be made fom triple layered light weight fabric with a well ventilated system of interconnected holes. Should accomodate bulky casts and provide maximum support to the injured arm. Should have super soft cushion adjustable pad to ensure a very high level of comfort & least pressure on the shoulders. Y clamp hook fasteners to ensure customized sizing of the sling (Medium) | As per colomn No.2 |
337 | Pouch Arm Sling Urbane (US FDA Certified – Registration No -):- Should be made fom triple layered light weight fabric with a well ventilated system of interconnected holes. Should accomodate bulky casts and provide maximum support to the injured arm. Should have super soft cushion adjustable pad to ensure a very high level of comfort & least pressure on the shoulders. Y clamp hook fasteners to ensure customized sizing of the sling (Large) | As per colomn No.2 |
338 | Pouch Arm Sling Urbane (US FDA Certified – Registration No -):- Should be made fom triple layered light weight fabric with a well ventilated system of interconnected holes. Should accomodate bulky casts and provide maximum support to the injured arm. Should have super soft cushion adjustable pad to ensure a very high level of comfort & least pressure on the shoulders. Y clamp hook fasteners to ensure customized sizing of the sling (XL) | As per colomn No.2 |
339 | Ankle Binder (US FDA Certified – Registration No -):- Should have a 3D knitting with a mellowed heel spot to ensure snug fitting, strong compression, comfortable ankle movement & perfect conformance to the complex anatomy of the ankle. Should have an elasticized wrap in figure of 8 to stabilize the ankle, control inversion/aversion & PF. Should contain dermophillic cotton to ensure comfort in all weather conditions and Nylon outside to ensure durability & aesthetics. (Small) | As per colomn No.2 |
340 | Ankle Binder (US FDA Certified – Registration No -):- Should have a 3D knitting with a mellowed heel spot to ensure snug fitting, strong compression, comfortable ankle movement & perfect conformance to the complex anatomy of the ankle. Should have an elasticized wrap in figure of 8 to stabilize the ankle, control inversion/aversion & PF. Should contain dermophillic cotton to ensure comfort in all weather conditions and Nylon outside to ensure durability & aesthetics. (Medium) | As per colomn No.2 |
341 | Ankle Binder (US FDA Certified – Registration No -):- Should have a 3D knitting with a mellowed heel spot to ensure snug fitting, strong compression, comfortable ankle movement & perfect conformance to the complex anatomy of the ankle. Should have an elasticized wrap in figure of 8 to stabilize the ankle, control inversion/aversion & PF. Should contain dermophillic cotton to ensure comfort in all weather conditions and Nylon outside to ensure durability & aesthetics. (Large) | As per colomn No.2 |
342 | Ankle Binder (US FDA Certified – Registration No -):- Should have a 3D knitting with a mellowed heel spot to ensure snug fitting, strong compression, comfortable ankle movement & perfect conformance to the complex anatomy of the ankle. Should have an elasticized wrap in figure of 8 to stabilize the ankle, control inversion/aversion & PF. Should contain dermophillic cotton to ensure comfort in all weather conditions and Nylon outside to ensure durability & aesthetics. (XL) | As per colomn No.2 |
343 | Ankle Brace (US FDA Certified – Registration No -):- Should be made of PUF fused, matte fabric body to ensure durability, high cushioning, enhanced comfort & pleasing aesthetics. Should provide triple stabilization through hook loop closure, lace tightening & rigid splinting to ensure firm protection. Apart from strong immobilization of both dorsi & plantar flexion movements, it should provide sufficient room for the malleolus. (CH) | As per colomn No.2 |
344 | Ankle Brace (US FDA Certified – Registration No -):- Should be made of PUF fused, matte fabric body to ensure durability, high cushioning, enhanced comfort & pleasing aesthetics. Should provide triple stabilization through hook loop closure, lace tightening & rigid splinting to ensure firm protection. Apart from strong immobilization of both dorsi & plantar flexion movements, it should provide sufficient room for the malleolus. (Small) | As per colomn No.2 |
345 | Ankle Brace (US FDA Certified – Registration No -):- Should be made of PUF fused, matte fabric body to ensure durability, high cushioning, enhanced comfort & pleasing aesthetics. Should provide triple stabilization through hook loop closure, lace tightening & rigid splinting to ensure firm protection. Apart from strong immobilization of both dorsi & plantar flexion movements, it should provide sufficient room for the malleolus. (Medium) | As per colomn No.2 |
346 | Ankle Brace (US FDA Certified – Registration No -):- Should be made of PUF fused, matte fabric body to ensure durability, high cushioning, enhanced comfort & pleasing aesthetics. Should provide triple stabilization through hook loop closure, lace tightening & rigid splinting to ensure firm protection. Apart from strong immobilization of both dorsi & plantar flexion movements, it should provide sufficient room for the malleolus. (Large) | As per colomn No.2 |
347 | Ankle Brace (US FDA Certified – Registration No -):- Should be made of PUF fused, matte fabric body to ensure durability, high cushioning, enhanced comfort & pleasing aesthetics. Should provide triple stabilization through hook loop closure, lace tightening & rigid splinting to ensure firm protection. Apart from strong immobilization of both dorsi & plantar flexion movements, it should provide sufficient room for the malleolus. (XL) | As per colomn No.2 |
348 | PF Night Splint Derotation (US FDA Certified – Registration No -):- Should have a highly functional design wherein degree of dorsiflexion can be customized. Molded foot casing to ensure full protection to ankle & foot and maintain ankle in neutral position. Should have a removable DEROTATION BAR to arrest the rotation of leg in post operative care. Should be light in weight with bilateral symmetry that can be used as a night splint & an ambulatory day splint. (Small, Medium, Large) | As per colomn No.2 |
349 | PF Night Splint Derotation (US FDA Certified – Registration No -):- Should have a highly functional design wherein degree of dorsiflexion can be customized. Molded foot casing to ensure full protection to ankle & foot and maintain ankle in neutral position. Should have a removable DEROTATION BAR to arrest the rotation of leg in post operative care. Should be light in weight with bilateral symmetry that can be used as a night splint & an ambulatory day splint. (Medium) | As per colomn No.2 |
350 | PF Night Splint Derotation (US FDA Certified – Registration No -):- Should have a highly functional design wherein degree of dorsiflexion can be customized. Molded foot casing to ensure full protection to ankle & foot and maintain ankle in neutral position. Should have a removable DEROTATION BAR to arrest the rotation of leg in post operative care. Should be light in weight with bilateral symmetry that can be used as a night splint & an ambulatory day splint. (Large) | As per colomn No.2 |
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