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| Sl. No. | Item Name |
| 1 | sps used in percatenous bladder with ballon complete set with silicone elastomer us-fda approved strictly size:8,12,16 fr |
| 2 | SPS-M used in percatenous bladder with ballon complete set with silicone elastomer US-FDA Approved strictly |
| 3 | SS-DPD WITH STOP COCK SET STRICTLY US-FDA APPROVED size:-12,14,16fr |
| 4 | UBD URETRACK FOR DILATION COMPLETE SET WITH DEVICE STRICTLY US-FDA APPROVED SIZE :-5 Fr/4cm, 5fr/10 cm LENGTH 70CM |
| 5 | TU- FOR DILATION COMPLETE SET WITH DEVICE STRICTLY US-FDA APPROVED 3.5/4frLENGTH70CMS |
| 6 | UDS-FOR STEP BY STEP INTRAMURAL TUNNEL AND URETER FOR MANIPULATION STRICTLY US-FDA APPROVED SIZE:-6,8,10,12,14,16 Fr LENGTH 60CMS |
| 7 | NT-Neprotrack for dilating stritly US-FDA Approved SIZE:-7/12fr LENGTH:55CMS |
| 8 | ARDS for progressive dilation for nephrostomy tract prior to precatinous SIZE:-8,10,12,14,16,18,20,24,26,28,30Fr LENGTH 30CMS |
| 9 | AM sheet used for maintaining tract Strictly US-FDA Approved SIZE:-20,22,24,26,28,30 Fr LENGTH 17CMS |
| 10 | Designed at a 130 degree angle to closely fit to the structure. Ensures angular stability by fixing the angle with plate to blade & shaft Accommodates standard 5.0 mm locking and shaft Minimizes the implant footprint , offering a compact alternative to three cannulated nailplate The implant offers up to 20 mm of controlled collapse, with end caps available in 6,8,10,12,14 and 16mm sizes 3.5 mm LCDCP plate 1 plate + 6 lock. Screw |
| 11 | Neuro Surgical Instrument - Smoke Evacuation System |
| 12 | A fully synthetic, biodegradable dermal regeneration dermal matrix/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 05x05cm |
| 13 | A fully synthetic, biodegradable dermal regeneration dermal matrix/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 06x08cm |
| 14 | A fully synthetic, biodegradable dermal regeneration dermal matrix/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 10x10cm |
| 15 | A fully synthetic, biodegradable dermal regeneration dermal matrix/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 10x20cm |
| 16 | A fully synthetic, biodegradable dermal regeneration dermal matrix/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 20x40cm |
| 17 | Biosynthetic skin protective layer as substitute which designed for advanced wound healing and burn management, providing an effective antimicrobial barrier to protect the wound and burn site while maintaining optimal moisture by balancing fluid and Gas level for faster healing. It should be biocompatible, suitable for use on partial- and full-thickness wounds, and capable of remaining in place throughout the healing process and promoting smooth development of new skin , it should be CE certified and manufactured under ISO 13485-certified quality management system. Size: 21 x 17 cm |
| 18 | Biosynthetic skin protective layer as substitute which designed for advanced wound healing and burn management, providing an effective antimicrobial barrier to protect the wound and burn site while maintaining optimal moisture by balancing fluid and Gas level for faster healing. It should be biocompatible, suitable for use on partial- and full-thickness wounds, and capable of remaining in place throughout the healing process and promoting smooth development of new skin , it should be CE certified and manufactured under ISO 13485-certified quality management system. Size: 8cm |
| 19 | Sterile wound irrigation solution containing 0.1 Percent Polyhexanide (PHMB) and 0.1 Percent Betaine surfactant, used for cleansing, moistening, and decontamination of acute and chronic wounds. Helps remove debris, slough, and biofilm without damaging healthy tissue. CE marked Class III Medical Device and FDA 510(k) cleared. Size: 1000ml |
| 20 | Sterile wound irrigation solution containing 0.1 Percent Polyhexanide (PHMB) and 0.1 Percent Betaine surfactant, used for cleansing, moistening, and decontamination of acute and chronic wounds. Helps remove debris, slough, and biofilm without damaging healthy tissue. CE marked Class III Medical Device and FDA 510(k) cleared.Size: 350ml |
| 21 | Sterile wound irrigation solution containing 0.1 Percent Polyhexanide (PHMB) and 0.1 Percent Betaine surfactant, used for cleansing, moistening, and decontamination of acute and chronic wounds. Helps remove debris, slough, and biofilm without damaging healthy tissue. CE marked Class III Medical Device and FDA 510(k) cleared.Size: 40ml |
| 22 | Dressing shall comprise 100 Percent native equine Type I collagen with an intact triple-helical conformation, ensuring optimal cellular signaling and ECM integration. Collagen mass per unit must be ≥150 mg, with zero excipients or denatured protein. The matrix must facilitate fibroblast chemotaxis, angiogenesis, and organized granulation. Product must demonstrate hemostatic function, exudate management, and microbial barrier properties. Size-10x10 CM |
| 23 | Dressing shall comprise 100 Percent native equine Type I collagen with an intact triple-helical conformation, ensuring optimal cellular signaling and ECM integration. Collagen mass per unit must be ≥150 mg, with zero excipients or denatured protein. The matrix must facilitate fibroblast chemotaxis, angiogenesis, and organized granulation. Product must demonstrate hemostatic function, exudate management, and microbial barrier properties. Size-5x5 CM |
| 24 | External device having single-component, 3-layer short stretch system with integrated epidermal contact, padding, and compression layers. It shall deliver sustained sub-bandage pressure of 40–60 mmHg with high working, low restingmaintain pressure for ≥7 days, and feature a built-in tension-limiting mechanism Safe-Loc to ensure uniform application. Fabric composition: 48 Percent polyamide, 42 Percent cotton, 6 Percent polyester, 4 Percent elastane. Size-10cmx6 mtr |
| 25 | External device having single-component, 3-layer short stretch system with integrated epidermal contact, padding, and compression layers. It shall deliver sustained sub-bandage pressure of 40–60 mmHg with high working, low resting maintain pressure for ≥7 days, and feature a built-in tension-limiting mechanism Safe-Loc to ensure uniform application. Fabric composition: 48 Percent polyamide, 42 Percent cotton, 6 Percent polyester, 4 Percent elastane. Size-8cmx6 mtr |
| 26 | Dressing shall be an open-cell polyurethane foam with uniform pore size (400–600 µm), compatible with advance NPWT systems. It must maintain dimensional stability and porosity under sustained negative pressure (-40 to -200 mmHg), enabling consistent exudate removal and promoting granulation tissue. Dressing must be sterile, latex-free, and CE-certified. Non-compatible or alternative foam types are strictly excluded. Size-Small,med,large |
| 27 | Dressing must be a sterile, self-adherent hydrocolloid composed of a hydrocolloid matrix (e.g., carboxymethylcellulose) laminated to a semi-permeable polyurethane film. It shall absorb low to moderate exudate, form a cohesive gel to maintain a moist wound environment, and support autolytic debridement. Dressing must remain intact for up to 7 days without maceration. Only dressings with proven occlusive properties and hydrocolloid integrity will be accepted. SIZE15X15 CM |
| 28 | Dressing must be a sterile, self-adherent hydrocolloid composed of a hydrocolloid matrix carboxymethylcelluloselaminated to a semi-permeable polyurethane film. It shall absorb low to moderate exudate, form a cohesive gel to maintain a moist wound environment, and support autolytic debridement. Dressing must remain intact for up to 7 days without maceration. Only dressings with proven occlusive properties and hydrocolloid integrity will be accepted.SIZE-10X10 CM |
| 29 | Dressing must be a sterile, self-adherent hydrocolloid composed of a hydrocolloid matrix (e.g., carboxymethylcellulose) laminated to a semi-permeable polyurethane film. It shall absorb low to moderate exudate, form a cohesive gel to maintain a moist wound environment, and support autolytic debridement. Dressing must remain intact for up to 7 days without maceration. Only dressings with proven occlusive properties and hydrocolloid integrity will be accepted. SIZE-20X20 CM |
| 30 | EU CE marked, EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test swaddle cloth with fluid absorbent nonwoven material Size 90x100 cm |
| 31 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test Bladder Scopy with perineal fenestration, centred Size 175x 90 cm |
| 32 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test Size 75x 120 cm,Non-woven Under Skirt and Layer With high-absorbency, fluid-impermeable nonwoven material with polyethylene backing, featuring ultrasonic-sealed edges for leak prevention surgical drape standards for single-use . |
| 33 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test Wrapping paper 90x100 cm, Vertical Swathe 230x320, towel 4 pcs 30x20, transparent PE film,with integrated incise film,30 x 40 with integrated fluid collection pouch incl. sieve and drainage port,with two tube retainers for retaining tubes and cords, Instrument pouch 20x30 |
| 34 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test Back Table Cover-150 X 190,Towels-30 X 40,Instrument Table Cover- Mayo Stand 80 x 145,Adhesive Strip-50X50,Swathe with Fenestration,with integrated fluid collection pouch, with lateral gutters incl. sieve and drainage port,with integrated tube fixations |
| 35 | Integrated skin protection in textile fabric layer - Soft compression bandage as first layer (10 cm*3.5 Metre & cohesive bandage short stretch as second layer with safe lock system (10 cm*6 Metre)CE & ISO Certified |
| 36 | Cohesive short Strech bandage for phlebology and lymphology which should be length wise elastic (to about 60 Percent) 99 Percent cotton,1 Percent synthetic thread with microdot natural rubber coting Size -10cmx6meter CE & ISO Certified |
| 37 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test (Dry & Wet),Resistance to liquid penetration test, Cleanliness test. (Microbial & Particulate matter),Bursting strength ( Dry & Wet),Tensile strength test ( Dry & Wet),Linting test.LAP Drape, 3-layered, 225 x 320, Fenestration, oval, lengthwise, off-centre, self-adhesive 11 x 22 |
| 38 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test (Dry & Wet),Resistance to liquid penetration test, Cleanliness test. (Microbial & Particulate matter),Bursting strength ( Dry & Wet),Tensile strength test ( Dry & Wet),Linting test.Spinal Drape, 3-layered, 225 x 320, Fenestration, oval, lengthwise, off-centre, self-adhesive 11 x 22 |
| 39 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test (Dry & Wet),Resistance to liquid penetration test, Cleanliness test. (Microbial & Particulate matter),Bursting strength ( Dry & Wet),Tensile strength test ( Dry & Wet),Linting test.Back Table Cover-150 X 190,4 Towels-30 X 40,Instrument Table Cover- Mayo Stand 80 x 145,Adhesive Strip-9x50, Baby drape, fluid-absorbent nonwoven material 90 x 90,C-section drape, for the supine position, 230/200 x 312, with abdominal fenestration, 27 x 33 with integrated incise film, with integrated fluid collection pouch incl. drainage port, with armrest cove |
| 40 | CE,ISO,TUV,EN13795 approved with certified test for, Resistance to Microbial Penetration test (Dry & Wet)Resistance to liquid penetration test, Cleanliness test. (Microbial & Particulate matter),Bursting strength ( Dry & Wet),Tensile strength test ( Dry & Wet),Linting test,Back Table Cover-150 X 190,Towels-30 X 20,Instrument Table Cover- Mayo Stand 80 x 145,Adhesive Strip-9 X 25,Adhesive Drapes Side-75 x 90,Adhesive Drapes- Bottom-175 x 170,Adhesive Drapes- Top-140 x 240 |
| 41 | CE,ISO,TUV,EN13795 approved with certified test for, Resistance to Microbial Penetration test (Dry & Wet),Resistance to liquid penetration test, Cleanliness test. (Microbial & Particulate matter),Bursting strength ( Dry & Wet),Tensile strength test ( Dry & Wet),Linting test. Back Table Cover-150 X 190,Towels-30 X 20,Adhesive Strip-9 X 25,Instrument Table Cover- Mayo Stand |
| 42 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test (Dry & Wet),Resistance to liquid penetration test, Cleanliness test. (Microbial & Particulate matter),Bursting strength ( Dry & Wet),Tensile strength test ( Dry & Wet),Linting test. Back Table Cover-150 X 190,Towels-30 X 20,Adhesive Strip-9 X 25,Instrument Table Cover- Mayo Stand-80 x 145,OT Drape Sheet-150x150Stockinette-33x55,Adhesive Film Strips-10x50,Extremity Drape-200x300 |
| 43 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test (Dry & Wet),Resistance to liquid penetration test, Cleanliness test. (Microbial & Particulate matter),Bursting strength ( Dry & Wet),Tensile strength test ( Dry & Wet),Linting test.Knee arthroscopy drape,225 x 320 cm, elastic fenestrations,6 + 7 cm with integrated fluid collection pouch incl. drainage port,with integrated tube fixations and hook-and-loop fastener |
| 44 | Special SMMS Surgical Gowns (XL) , CE,ISO,TUV,EN13795 marked, closer types with cuff AAMI Level 4 - Blood Penetration test ASTM F1670 &Viral Penetration test ASTM F1671\\" - 170 cm Size XL Long |
| 45 | Graduated Compression stockings below knee having pressure 23-33mmHg at Ankle. Should Be made up of 62 Percent TACTEL,26 Percent Lycra,8 Percent cotton and 4 Percent SEACELL active.Sizes-M |
| 46 | Graduated Compression stockings below knee having pressure 23-33mmHg at Ankle. Should Be made up of 62 Percent TACTEL,26 Percent Lycra,8 Percent cotton and 4 Percent SEACELL active.Sizes-L |
| 47 | Graduated Compression stockings below knee having pressure 23-33mmHg at Ankle.Should Be made up of 62 Percent TACTEL,26 Percent Lycra,8 Percent cotton and 4 Percent SEACELL active.Sizes-XL |
| 48 | Graduated Compression stockings below knee having pressure 23-33mmHg at Ankle.Should Be made up of 62 Percent TACTEL,26 Percent Lycra,8 Percent cotton and 4 Percent SEACELL active.Sizes-XXL |
| 49 | Graduated compression stockings with Above Knee having pressure gradient 16-18mmhs/material composition 91 Percentnylon polyamide,9 Percent lycra elastane,Color coding with extra gussette Size S |
| 50 | Graduated compression stockings with Above Knee having pressure gradient 16-18mmhs/material composition 91 Percentnylon polyamide,9 Percent lycra elastane,Color coding with extra gussette Size M |
| 51 | Graduated compression stockings with Above Knee having pressure gradient 16-18mmhs/material composition 91 Percentnylon polyamide,9 Percent lycra elastane,Color coding with extra gussette Size L |
| 52 | Graduated compression stockings with Above Knee having pressure gradient 16-18mmhs/material composition 91 Percentnylon polyamide,9 Percent lycra elastane,Color coding with extra gussette Size XL |
| 53 | Graduated compression stockings with Above Knee having pressure gradient 16-18mmhs/material composition 91 Percentnylon polyamide,9 Percent lycra elastane,Color coding with extra gussette Size XXL |
| 54 | rectangular shape and rounded corners with monitoring window, having MVTR in the area of fixation: 964 g / 24 h / m² ,die-cut opening, lengthwise elasticity additional sterile cushioning pad with fixation size-5.5x6.5 CM,CE & ISO Certified |
| 55 | Rectangular shape with rounded corners pure nonwoven Canula fixator size 6x7.5 CM, having die-cut opening lengthwise elasticity up to 0.6 N / 12 mm and wound pad 20 x 20 mm, CE & ISO Certified |
| 56 | CVC Dressing with ergonomic shape film with porous adhesive coating, monitoring window large film-nonwoven laminate counter fixation element with V-shaped cutout lengthwise elasticity additional sterile cushioning pad size 9x11 CM,CE & ISO Certified |
| 57 | wide retention polyester wound dressing having polyacrylate strip patterned adhesive coating with MVTR more than 5000 g/m2/24hr and air permeability more than 4000 g/m2/24hr SIZE 10cmx2m,CE & ISO Certified |
| 58 | wide retention polyester wound dressing having polyacrylate strip patterned adhesive coating with MVTR more than 5000 g/m2/24hr and air permeability more than 4000 g/m2/24hr. SIZE 10cmx10m,CE & ISO Certified |
| 59 | EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test (Dry & Wet),Resistance to liquid penetration test, Cleanliness test. (Microbial & Particulate matter),Bursting strength ( Dry & Wet),Tensile strength test ( Dry & Wet),Linting test.1 T.U.R. drape, 175/260 x 210, with integrated leggings, 125 perineal fenestration -5suprapubic opening-8 with integrated fluid collection pouchincl. sieve and drainage port, with latex-free finger stall |
| 60 | Class 1 EC Medical Device with Accuracy and waterproof adhesive thermochromic temperature indicator with three colour code |
| 61 | Central Venous Catheter adult 3 lumen 7Fr & 16 cm length with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 62 | Central Venous Catheter adult 3 lumen 7Fr & 15 cm length with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 63 | Central Venous Catheter adult 3 lumen 7Fr & 13 cm length with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 64 | Short Term Femoral Polyurithane Catheter with double lumen 11.5 Fr & 13 cm length, Soft PVC dilator for smooth insertion, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 65 | Short Term Jugular Polyurithane Catheter with double lumen 11.5 Fr & 13 cm length,Soft PVC dilator for smooth inserton, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 66 | Short Term Femoral Polyurithane Catheter with double lumen 12 Fr & 15 cm length, Soft PVC dilator for smooth insertion, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 67 | Short Term Jugular Polyurithane Catheter with double lumen 12 Fr & 15 cm length, Soft PVC dilator for smooth insertion,Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 68 | Short Term Femoral Polyurithane Catheter with triple lumen 12 Fr & 13 cm length, Soft PVC dilator for smooth insertion,Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 69 | Short Term Jugular Polyurithane Catheter with triple lumen 12 Fr & 13 cm length, Soft PVC dilator for smooth insertion, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 70 | Short Term Femoral Polyurithane Catheter with triple lumen 12 Fr & 16 cm length, Soft PVC dilator for smooth insertion,Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 71 | Short Term Jugular Polyurithane Catheter with triple lumen 12 Fr & 16 cm length, Soft PVC dilator for smooth insertion,Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 72 | trach Suction Tube - imported |
| 73 | CE approved advance system for inactivation of aerosolized virus through electromagnetic waves that resonate with virus outer shell until it breaks in open and close environment with PAC which cover 50 Sq mtr area. type1 |
| 74 | CE approved advance system for inactivation of aerosolized virus through electromagnetic waves that resonate with virus outer shell until it breaks in open and close environment with PAC which cover 50 Sq mtr area.type2 |
| 75 | CE approved advance system for inactivation of aerosolized virus through electromagnetic waves that resonate with virus outer shell until it breaks in open and close environment with PAC which cover 3 Sq mtr area.type1 |
| 76 | CE approved advance system for inactivation of aerosolized virus through electromagnetic waves that resonate with virus outer shell until it breaks in open and close environment with PAC which cover 3 Sq mtr area.type2 |
| 77 | Special SMMS Surgical Gowns (XL) : CE,ISO,TUV,EN13795 marked, closer types with cuff - Blood Penetration test ASTM F1670 &Viral Penetration test ASTM F1671\\" AAMI 3 |
| 78 | Transparent Carrier film 100 Percent polyurethane, skin-friendly polyacrylate adhesive with free of colophony and colophony derivatives and Wound pad with absorbent layer made of viscose/polyester, polyester/poly-ethylene wound contact 2.8x 2 Inch,CE & ISO Certified |
| 79 | Transparent Carrier film 100 Percent polyurethane, skin-friendly polyacrylate adhesive with free of colophony and colophony derivatives and Wound pad with absorbent layer made of viscose/polyester, polyester/poly-ethylene wound contact 4x3.2 Inch,CE & ISO Certified |
| 80 | Transparent Carrier film 100 Percent polyurethane, skin-friendly polyacrylate adhesive with free of colophony and colophony derivatives and Wound pad with absorbent layer made of viscose/polyester, polyester/poly-ethylene wound contact 4x6 Inch,CE & ISO Certified |
| 81 | Transparent Carrier film 100 Percent polyurethane, skin-friendly polyacrylate adhesive with free of colophony and colophony derivatives and Wound pad with absorbent layer made of viscose/polyester, polyester/poly-ethylene wound contact 4x8 Inch,CE & ISO Certified |
| 82 | Transparent Carrier film 100 Percent polyurethane, skin-friendly polyacrylate adhesive with free of colophony and colophony derivatives and Wound pad with absorbent layer made of viscose/polyester, polyester/poly-ethylene wound contact 4x10 Inch,CE & ISO Certified |
| 83 | Front fastetnig short stretch material strap, with block pattern for structural support, with liner easy for easy donning 2 step design with color coded velcro for calf M |
| 84 | Front fastetnig short stretch material strap, with block pattern for structural support, with liner easy for easy donning 2 step design with color coded velcro for calf L |
| 85 | Front fastetnig short stretch material strap, with block pattern for structural support, with liner easy for easy donning 2 step design with color coded velcro for calf XL |
| 86 | Turbojet Closed suction cathter MDI Port has Isolated turbo cleaning chamber for cleaning cathter tip with MDI Port.Catheter is made up of medical grade silicon.Catheter has jig-jag port for better Available in both Endotracheal and Trachiostomy verson can be used for 72 hourssuctioning.Tween Peep Seals.Available in both Endotracheal and Trachiostomy verson can be used for 72 hoursSizes 12TT |
| 87 | Turbojet Closed suction cathter MDI Port has Isolated turbo cleaning chamber for cleaning cathter tip with MDI Port.Catheter is made up of medical grade silicon.Catheter has jig-jag port for better Available in both Endotracheal and Trachiostomy verson can be used for 72 hourssuctioning.Tween Peep Seals.Available in both Endotracheal and Trachiostomy verson can be used for 72 hoursSizes,12ET |
| 88 | Turbojet Closed suction cathter MDI Port has Isolated turbo cleaning chamber for cleaning cathter tip with MDI Port.Catheter is made up of medical grade silicon.Catheter has jig-jag port for better Available in both Endotracheal and Trachiostomy verson can be used for 72 hourssuctioning.Tween Peep Seals.Available in both Endotracheal and Trachiostomy verson can be used for 72 hoursSizes,14ET |
| 89 | Turbojet Closed suction cathter MDI Port has Isolated turbo cleaning chamber for cleaning cathter tip with MDI Port.Catheter is made up of medical grade silicon.Catheter has jig-jag port for better Available in both Endotracheal and Trachiostomy verson can be used for 72 hourssuctioning.Tween Peep Seals.Available in both Endotracheal and Trachiostomy verson can be used for 72 hoursSizes,14TT |
| 90 | ANTIMICROBIAL FINE MIST FOGGING SOLUTION 5 LITERS ANTI CORRISIVE ce CERTIFIED FORMALDEHYDE FREE |
| 91 | HYDRA NEG WIRE 0.025 ANGULATED CE CERTIFIED /USFDA certified for ERCP |
| 92 | HYDRA NEG WIRE 0.025 J TIPCE CERTIFIED/USFDA certified for ERCP |
| 93 | HYDRA NEG WIRE 0.025 STRAIGHT CE CERTIFIED/USFDA certified for ERCP |
| 94 | HYDRA NEG WIRE 0.032 ANGULATED CE CERTIFIED/USFDA certified for ERCP |
| 95 | HYDRA NEG WIRE 0.032 J TIP CE CERTIFIED/USFDA certified for ERCP |
| 96 | HYDRA NEG WIRE 0.032 STRAIGNT CE CERTIFIED/USFDA certified for ERCP |
| 97 | HYDRA NEG WIRE 0.035 ANGULATED CE CERTIFIED/USFDA certified for ERCP |
| 98 | HYDRA NEG WIRE 0.035 J TIP CE CERTIFIED/USFDA certified for ERCP |
| 99 | HYDRA NEG WIRE 0.035 STRAIGHT CE CERTIFIED/USFDA certified for ERCP |
| 100 | Cassettes for Plasma Sterilization Machine 1x2 cassettes per box, the plastic cassettes should contain approx 58-59.5 Percent hydrogen peroxide sterilant., -Each cassette should contain 10 cells of 1.8 ml of Hydrogen peroxide, Each cassette should run atleast 5 cycles, -Expiry date should be approx 6 months from the date of manufacturing -Colour bar must indicate exposure to leakage (in case of H2O2 leak) -it should change colour from yellow to red -It should be compatible to Sterrad 100 NX. |
| 101 | Chemical Indicator tape on exposure of hydrogen peroxide post sterilization result in recognizable color change from red to yellow. The product must be endorsed by USFDA/510K or European CE. (Pack of 1000 strips) |
| 102 | Chemical Indicator tape on exposure of hydrogen peroxide post sterilization result in recognizable color change from red to yellow. Adhesive strength studies should confirm that the tape has adequate preprocessing and post-processing adhesive properties to support and extension of the product to 22 months. This should be endorsed by USFDA/510k or European CE. (Pack of 6) |
| 103 | TYVEK Pouch Roll 7.5 cm X 70 m(Pack of 6) with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. It should be validated to use in Sterrad Plasma Sterilizer. |
| 104 | TYVEK Pouch Roll 10 cm X 70 m (Pack of 6) with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE It should be validated to use in Sterrad Plasma Sterilizer. |
| 105 | TYVEK Pouch Roll 15 cm X 70 m (Pack of 4) with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CEIt should be validated to use in Sterrad Plasma Sterilizer. |
| 106 | TYVEK Pouch Roll 20 cm X 70 m (Pack of 4) with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE It should be validated to use in Sterrad Plasma Sterilizer. |
| 107 | TYVEK Pouch Roll 25 cm X 70 m (Pack of 4) with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE It should be validated to use in Sterrad Plasma Sterilizer. |
| 108 | TYVEK Pouch Roll 35 cm X 70 m (Pack of 2) with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE It should be validated to use in Sterrad Plasma Sterilizer. |
| 109 | Biological indicator with fluorescence abstract technology able to give results in 15 to 30 min. Should have chemical indicator on top for Biological Indicator(BI) confirmation with barcode/QR code for Identification and tracking. The BI Should be Compatible with quoted Plasma Sterilizer. Resistance characteristics of Biological Indicator - Tested at 5 mg/L hydrogen peroxide; D-value 5mg/L: ≥ 1 second, using two D-value methods (Survivor Curve and Fraction Negative) per ISO 11138-1 which should be endorsed by USFDA/510K or European CE. (Pack of 30) |
| 110 | BI Reader with ability to read BI to obtain fluorescence in 15 mins at the incubation temperature of 57 ± 2⁰C. Should have barcode reader to track and identify the Biological indicator. Should have a compatible printer for report documentation. Should have audio visual alarm with touch screen for user interface and command. Should have USB/ ethernet connection for data management. Should have USFDA/ 510K/ European CE. (Pack of 1) |
| 111 | TYVEK Self seal Pouch 3” X 8” with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE (Pack of 500) It should be validated to use in Sterrad Plasma Sterilizer. |
| 112 | TYVEK Self seal Pouch 4” X 10.25” with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE (Pack of 500)It should be validated to use in Sterrad Plasma Sterilizer. |
| 113 | TYVEK Self seal Pouch 6” X 12.5” with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE It should be validated to use in Sterrad Plasma Sterilizer. |
| 114 | TYVEK Self seal Pouch 4” X 14” with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE (Pack of 500) It should be validated to use in Sterrad Plasma Sterilizer. |
| 115 | TYVEK Self seal Pouch 8” X 16” with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE (Pack of 500) It should be validated to use in Sterrad Plasma Sterilizer. |
| 116 | TYVEK Self seal Pouch 6” X 16.5” with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE (Pack of 500) It should be validated to use in Sterrad Plasma Sterilizer. |
| 117 | TYVEK Self seal Pouch 10” X 19” with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE (Pack of 400) It should be validated to use in Sterrad Plasma Sterilizer. |
| 118 | TYVEK Self seal Pouch 12.5” X 22” with inbuilt Chemical Indicator strip should be compatible for use in Plasma Sterilizer which should be endorsed by USFDA/510K or European CE. Tyvek of grade 4057B should be provided with three independent barriers. In Vivo testing pouch should demonstrate that the pouch samples after processing in sterilizer should meet the acceptance criteria as per ISO 10993-11 and 10993-10 and can be safely used. Seal strength test, microbial barrier properties, burst test and peel open test demonstrated acceptable material compatibility characteristics of the Tyvek Pouches/Rolls after processing in the Plasma Sterilizer which should be endorsed by USFDA/510K or European CE (Pack of 400) It should be validated to use in Sterrad Plasma Sterilizer. |
| 119 | Instrument Tray of size 12”X 4”X2” designed to encase surgical instruments for sterilization in steam, ethylene oxide and Plasma sterilization system. The tray is designed with a high perforation area on the lid, base and side panels to enhance diffusion of sterilant during sterilization. The hole size and spacing is the same in all trays to enable the use of a common design instrument tray mats and holders. The material compatibility studies should include residual testing of trays following ETO sterilization, material compatibility of the tray with steam sterilization processing and material compatibility of the tray in Plasma sterilization system which should be validated by USFDA/510K or European CE It should be validated to use in Sterrad Plasma Sterilizer. |
| 120 | Instrument Tray of size 18”X4”X2” designed to encase surgical instruments for sterilization in steam, ethylene oxide and Plasma sterilization system. The tray is designed with a high perforation area on the lid, base and side panels to enhance diffusion of sterilant during sterilization. The hole size and spacing is the same in all trays to enable the use of a common design instrument tray mats and holders. The material compatibility studies should include residual testing of trays following ETO sterilization, material compatibility of the tray with steam sterilization processing and material compatibility of the tray in Plasma sterilization system which should be validated by USFDA/510K or European CE (Pack of 2) |
| 121 | Instrument Tray of size 24”X 4”X2” designed to encase surgical instruments for sterilization in steam, ethylene oxide and Plasma sterilization system. The tray is designed with a high perforation area on the lid, base and side panels to enhance diffusion of sterilant during sterilization. The hole size and spacing is the same in all trays to enable the use of a common design instrument tray mats and holders. The material compatibility studies should include residual testing of trays following ETO sterilization, material compatibility of the tray with steam sterilization processing and material compatibility of the tray in Plasma sterilization system which should be validated by USFDA/510K or European CE (Pack of 2) |
| 122 | Instrument Tray of size 12”X 8”X2” designed to encase surgical instruments for sterilization in steam, ethylene oxide and Plasma sterilization system. The tray is designed with a high perforation area on the lid, base and side panels to enhance diffusion of sterilant during sterilization. The hole size and spacing is the same in all trays to enable the use of a common design instrument tray mats and holders. The material compatibility studies should include residual testing of trays following ETO sterilization, material compatibility of the tray with steam sterilization processing and material compatibility of the tray in Plasma sterilization system which should be validated by USFDA/510K or European CE (Pack of 2) |
| 123 | Instrument Tray of size 18”X8”X2” designed to encase surgical instruments for sterilization in steam, ethylene oxide and Plasma sterilization system. The tray is designed with a high perforation area on the lid, base and side panels to enhance diffusion of sterilant during sterilization. The hole size and spacing is the same in all trays to enable the use of a common design instrument tray mats and holders. The material compatibility studies should include residual testing of trays following ETO sterilization, material compatibility of the tray with steam sterilization processing and material compatibility of the tray in Plasma sterilization system which should be validated by USFDA/510K or European CE (Pack of 2) |
| 124 | Instrument Tray of size 24”X 8”X 2” designed to encase surgical instruments for sterilization in steam, ethylene oxide and Plasma sterilization system. The tray is designed with a high perforation area on the lid, base and side panels to enhance diffusion of sterilant during sterilization. The hole size and spacing is the same in all trays to enable the use of a common design instrument tray mats and holders. The material compatibility studies should include residual testing of trays following ETO sterilization, material compatibility of the tray with steam sterilization processing and material compatibility of the tray in Plasma sterilization system which should be validated by USFDA/510K or European CE |
| 125 | Instrument Tray of size 11”X 10.6”X 4” designed to encase surgical instruments for sterilization in steam, ethylene oxide and Plasma sterilization system. The tray is designed with a high perforation area on the lid, base and side panels to enhance diffusion of sterilant during sterilization. The hole size and spacing is the same in all trays to enable the use of a common design instrument tray mats and holders. The material compatibility studies should include residual testing of trays following ETO sterilization, material compatibility of the tray with steam sterilization processing and material compatibility of the tray in Plasma sterilization system which should be validated by USFDA/510K or European CE (Pack of 2) |
| 126 | Instrument Tray of size 23”X 11”X 4” designed to encase surgical instruments for sterilization in steam, ethylene oxide and Plasma sterilization system. The tray is designed with a high perforation area on the lid, base and side panels to enhance diffusion of sterilant during sterilization. The hole size and spacing is the same in all trays to enable the use of a common design instrument tray mats and holders. The material compatibility studies should include residual testing of trays following ETO sterilization, material compatibility of the tray with steam sterilization processing and material compatibility of the tray in Plasma sterilization system which should be validated by USFDA/510K or European CE (Pack of 2) |
| 127 | ENDOSCOPE HOLDER 0.4\\" x 0.8\\" x 0.4” designed to encase ENDOSCOPE for in instrument trays. The product must be USFDA or European CE certified. (Pack of 4) |
| 128 | ENDOSCOPE HOLDER 0.8\\" x 0.4\\" x 0.8” designed to encase ENDOSCOPE for in instrument trays. The product must be USFDA or European CE certified. (Pack of 4) |
| 129 | ENDOSCOPE HOLDER 0.2\\" x 0.8\\" x 0.2” designed to encase ENDOSCOPE for in instrument trays. The product must be USFDA or European CE certified. (Pack of 4) |
| 130 | ENDOSCOPE HOLDER 0.8\\" x 0.2\\" x 0.8” designed to encase ENDOSCOPE for in instrument trays. The product must be USFDA or European CE certified. (Pack of 4) |
| 131 | ENDOSCOPE HOLDER 0.4\\" x 0.4\\" x 0.4” designed to encase ENDOSCOPE for in instrument trays. The product must be USFDA or European CE certified. (Pack of 4) |
| 132 | ENDOSCOPE HOLDER 0.6\\" x 0.6\\" x 0.6” designed to encase ENDOSCOPE for in instrument trays. The product must be USFDA or European CE certified. (Pack of 4) |
| 133 | ENDOSCOPE HOLDER 0.2\\" x 0.2\\" x 0.2” designed to encase ENDOSCOPE for in instrument trays. The product must be USFDA or European CE certified. (Pack of 4) |
| 134 | Holding Bar designed to encase ENDOSCOPE for in instrument trays. The product must be USFDA or European CE certified. (Pack of 4) |
| 135 | Tray with lid and liner for manual cleaning and high level disinfection. The trays have to heat resistant up to 134 degree celsius. They have to be made with glas filled polypropylene for superior durability. Size 740 mm x 220 mm x 132 mm equal to 14.1 liters |
| 136 | Tray with lid and liner for manual cleaning and high level disinfection. The trays have to heat resistant up to 134 degree celsius. They have to be made with glas filled polypropylene for superior durability. 449mm Diameter by 222mm equal to 17.5 liters |
| 137 | Tray with lid and liner for manual cleaning and high level disinfection. The trays have to heat resistant up to 134 degree celsius. They have to be made with glas filled polypropylene for superior durability. Size 594 mm x 381 mm x 141 mm equal to 19.8 liters |
| 138 | A Low foaming with mild pH solution enzymatic anionic detergent with rust inhibitors used for manual as well as automated system containing four enzymes viz; Bacterial Protease, lipase, Amylase and cellulase. Manual soak time for highly soiled instruments should be less than 4 minutes. The product has to be biodegradable. |
| 139 | Liquid Reagent used for high level disinfection with 2.45 Percent w/v Glutaraldehyde and MEC level of 1.5 Percent with a powder activator. Should have validated test strips with the manufacturer to test MEC/efficacy of the same manufacturer. The solution should be recommended by minimum 3 leading IFUs of reputed telescopes manufacturers (e.g. Richard Wolf, Karl Storz, Olympus, Stryker, Smith & Nephew, etc.) for reporecessing their telescopes. 1 jar of 5 ltrs to be quoted. |
| 140 | 0.55 Percent orthophthalaldehyde with pH 7.2 -7.8 and water soluble with immersion time for high level disinfection not higher than five minutes; Should have validated test strips with the manufacturer to test MEC/efficacy of the same manufacturer. The solution should be recommended by the leading IFUs of minimun three reputed telescope manufacturers (e.g. Karl Storz, Olympus, Stryker, Smith & Nephew, etc.) for reporecessing their scopes. 1 jar of 5 ltrs to be quoted. |
| 141 | Cassettes for Plasma Sterilization Machine -1x5 cassettes per box, the plastic cassettes should contain approx 58-59.5 Percent hydrogen peroxide sterilant., -Each cassette should contain 10 cells of 1.8 ml of Hydrogen peroxide, Each cassette should run atleast 5 cycles, -Expiry date should be approx 6 months from the date of manufacturing -Colour bar must indicate exposure to leakage (in case of H2O2 leak) -it should change colour from yellow to red -It should be compatible to Sterrad Machines |
| 142 | Automatic Reader for Self-Contained BiologicalIndicators1. Universal BI reader for Steam, ETO and VH2O2 equipped with a built-in ampoule crusher to activate the biological indicators within the reader which eliminates the need for a separate tool and a color touchscreen display that allows direct user interaction, real-time monitoring of incubation status, temperature conditions, alerts, and system functions2. It should have minimum 12 wells for incubation3. Complete BI PCD records with build-in system printer each time an incubation is completed, allowing for easy result management and compliance documentation4. The BI reader must have an integrated data storage system capable of storing 200+ results and displaying historical BI test results on the device itself. 5. The reader must also support direct printing of stored results from the reader without requiring any external software, web application, or network connection.6. Faster BI readout time in steam sterilization monitoring should be 20 minutes 7. It should be USFDA endorsed product8. Compatible BIs to have minimum 24 months shelf life from the date of manufacturing |
| 143 | Steam BI with readout time in less than or equal to 20 mins1. A self-contained biological indicator(SCBI) inoculated with viable 106 Geobacillus stearothermophilus bacterial spores and is intended formonitoring the efficacy of steam sterilization processes. On each Steam Biological Indicator is a chemical process indicator that changes color from pink to brownwhen exposed to steam.2. It should been designed for quick and easy monitoring of vacuum assisted and gravity displacement steam sterilization cycles at 132-135 °C (269.6-275 °F).3. SCBI should have Type 1 chemical indicator on label, allowing the user to differentiate between biological indicators that have been processed (brown) versus unprocessed (pink) biological indicators.4. Fluorescence readout: 20 minutes Readout must be carried out in the compatible universal reader for Steam, ETO and VH2O2 equipped with a built-in ampoule crusher, color touchscreen display, built in printer and ability to store 200+ test results. 5. It should comply with ISO 11138-1 & ISO 11138-3 6. The product should be endorsed by USFDA7. The total shelf life from manufacturing should be minimum 2 years Price should be quoted for 1 unit. |
| 144 | Steam BI with readout time in less than or equal to 60 mins1. A self-contained biological indicator(SCBI) inoculated with viable 106 Geobacillus stearothermophilus bacterial spores and is intended formonitoring the efficacy of steam sterilization processes. On each Steam Biological Indicator is a chemical process indicator that changes color from pink to brownwhen exposed to steam.2. It should been designed for quick and easy monitoring of vacuum assisted and gravity displacement steam sterilization cycles at 121-135 °C (249.8-275 °F).3. SCBI should have Type 1 chemical indicator on label, allowing the user to differentiate between biological indicators that have been processed (brown) versus unprocessed (pink) biological indicators.4. Fluorescence readout: 60 minutes Readout must be carried out in the compatible universal reader for Steam, ETO and VH2O2 equipped with a built-in ampoule crusher, color touchscreen display, built in printer and ability to store 200+ test results. 5. It should comply with ISO 11138-1 & ISO 11138-3 6. The product should be endorsed by USFDAThe total shelf life from manufacturing should be minimum 2 years Price should be quoted for 1 unit. |
| 145 | EO BI with readout time in less than or equal to 4 hours1. A self-contained biological indicator(SCBI) inoculated with viable 106 Bacillus Atropheus bacterial spores and is intended for monitoring the efficacy of ethylene oxide sterilization processes cycle 55 ˚C for 240 minutes, 600 mg/l, RH 60 Percent.2. SCBI should have Type 1 chemical indicator on label, allowing the user to differentiate between biological indicators that have been processed (brown) versus unprocessed (green) biological indicators.3. Fluorescence readout: 60 minutes Readout must be carried out in the compatible universal reader for Steam, ETO and VH2O2 equipped with a built-in ampoule crusher, color touchscreen display, built in printer and ability to store 200+ test results. 4. It should comply with ISO 11138-1 & ISO 11138-3 5. The product should be endorsed by USFDA6. The total shelf life from manufacturing should be minimum 2 years Price should be quoted for 1 unit. |
| 146 | Steam Type 4 Multi-Variable Chemical Indicator1. It should be single-use chemical indicator that consist of one-side laminated perforated paper double strips printed with indicator ink. These indicators should be designed to monitor steam sterilization processes within loads, ensuring an acceptable exposure to the sterilizing agent during the sterilization process. A highly sensitive yellow ink should be used to turn to dark brown/black when the indicator is exposed to steam considering the critical process variables (steam, time, and temperature) which provides additional quality assurance.2. The material should be heavy metal-free and not made with natural rubber latex3. It should feature an easy-to-scan barcode for automatic entry of lot and expiration dates into instrument tracking systems.4. It should comply with ISO 11140-1:2014 (Type 4) 5. The product should be endorsed by USFDA6. The total shelf life from manufacturing should be minimum 60 months Price should be quoted for 1 unit. |
| 147 | Steam Type 5 Migrating Integrator1.Steam Type 5 Migrating Integrator should be single-use moving front chemical indicators for monitoring steam sterilization processes. These indicators ensure an adequate control of the effectiveness of steam sterilization processes by monitoring all critical parameters. Steam Type 5 Migrating Integrator should consist of a special paper wick and a steam and temperature sensitive chemical pellet contained in a paper/film/foil laminate. The chemical pellet should melt and migrate as a dark bar along the paper wick. The migration should be visible through a zone marked ACCEPT or REJECT, thus indicating whether sterilization conditions were met. The extent of migration depends on steam quality, time and temperature. The ACCEPT result is reached when a theoretical spore population reaches its kill time, indicating integration condition has been reached. This condition should be calibrated with the kill time of a 106 Geobacillus stearothermophilus ATCCR 7953 spores population, calculated in BIER (Biological Indicator Evaluator Resistometer).1. It should feature an easy-to-scan barcode for automatic entry of lot and expiration dates into instrument tracking systems.2. It should comply with ISO 11140-1:2014 (Type 5) 3. The product should be endorsed by USFDAThe total shelf life from manufacturing should be minimum 60 months Price should be quoted for 1 unit. |
| 148 | Steam Type 5 Ink Integrator1. Steam Type 5 Ink Integrator should be single-use unique point chemical indicators that consist of paper strips printed with indicator ink. They should be designed for steam sterilization processes, ensuring an adequate control of the effectiveness of sterilization processes. Yellow ink should turn to black when a theoretical spore population reaches its kill time, indicating the integration condition has been reached. This condition should be calibrated with the kill time of a 106 Geobacillus stearothermophilus ATCCR 7953 spore population, calculated in BIER (Biological Indicator Evaluator Resistometer).2. The material should be heavy metal-free and not made with natural rubber latex3. It should feature an easy-to-scan barcode for automatic entry of lot and expiration dates into instrument tracking systems.4. It should comply with ISO 11140-1:2014 (Type 5) 5. The product should be endorsed by USFDA6. The total shelf life from manufacturing should be minimum 60 months Price should be quoted for 1 unit. |
| 149 | Bowie Dick Test Card1. Bowie-Dick Test Card indicator should be supplied with a reusable holder. Bowie-Dick Test Card (73196) should be used to evaluate the effectiveness of air removal during pre-vacuum steam sterilization cycles operating at 134 °C (273.2 °F), 3.5 minutes / 132 °C, 4 minutes (269.6 °F). Bowie-Dick Test Card air-removal indicator card should be used with its reusable holder. The indicator should uniformly turn from purple to green when processed correctly. If a heterogeneous color change occurs in the indicator, it is an indication of the presence of residual air in the chamber and, therefore, sterilizer malfunction. Cycle information can be recorded on the back of the indicator, thus allowing a permanent record of the process.2. The Bowie-Dick Test Card should comply with ISO 11140-1:2014 and ISO 11140-4:2007 standards.3. It should feature an easy-to-scan barcode for automatic entry of lot and expiration dates into instrument tracking systems.4. The product should be endorsed by USFDAThe total shelf life from manufacturing should be minimum 60 months Steam Type 5 Ink Integrator1. Steam Type 5 Ink Integrator should be single-use unique point chemical indicators that consist of paper strips printed with indicator ink. They should be designed for steam sterilization processes, ensuring an adequate control of the effectiveness of sterilization processes. Yellow ink should turn to black when a theoretical spore population reaches its kill time, indicating the integration condition has been reached. This condition should be calibrated with the kill time of a 106 Geobacillus stearothermophilus ATCCR 7953 spore population, calculated in BIER (Biological Indicator Evaluator Resistometer).2. The material should be heavy metal-free and not made with natural rubber latex3. It should feature an easy-to-scan barcode for automatic entry of lot and expiration dates into instrument tracking systems.4. It should comply with ISO 11140-1:2014 (Type 5) 5. The product should be endorsed by USFDA5. The total shelf life from manufacturing should be minimum 60 months Price should be quoted for 1 unit. |
| 150 | Bowie Dick Test Pack1. Bowie-Dick Test Pack should detect air leaks, inadequate air removal and steam penetration level in vacuum-assisted steam sterilizers. The Bowie-Dick Test Pack should consist of a chemical indicator sheet (125 mm x 125 mm) between porous material sheets and wrapped forming a package, with a steam indicator label. The central sheet, with a regular pattern, corresponds to a Bowie-Dick classic indicator, i.e. BD Test Sheet. The central sheet chemical indicator changes from yellow to dark brown/black when processed. Any unexpected color change, such as lighter areas in the center of the sheet or different colors in the edges (i.e., a non-uniform color change) indicates an air pocket during the cycle due to sterilizer malfunction.2. The Bowie-Dick Test Pack should comply with ISO 11140-1:2014 and ISO 11140-4:2007 standards.3. It should feature an easy-to-scan barcode for automatic entry of lot and expiration dates into instrument tracking systems.4. The product should be endorsed by USFDAThe total shelf life from manufacturing should be minimum 60 months. Price should be quoted for 1 unit. |
| 151 | Germicidal whole body washing. Octenidine based wash lotion with neutral pH aqua,cocamidopropylamine oxide, PEG-7 glyceryl cocoate,glycerin, hydroxyethyl-cellulose, lactic acid, containsallantoin 500 ML |
| 152 | Hygienic Hand disinfection &Surgical Hand Disinfection Each 100 g contains:2-propanol IP: 45 g / Isopropanol1-propanol: 30 g /n- propanolEthyl-hexadecyl-dimethyl-ammonium-ethylsulphate: 0.2 g Emollient and Moisturiser with skin protecting substances 500 ml Bott with dispenserPasses EN 13727, EN13624, EN14476, EN1500, EN12791 Standards Shelf life 2 Years. Pack size 5 Ltr. |
| 153 | Hygienic Hand disinfection &Surgical Hand Disinfection Each 100 ml contains Ethanol IP 79.9 Percent v/v in a gel basePasses EN standards including EN 1500, EN 12791, EN 13727, EN 13624, EN 14476 Selflife 2 years. Pack Size 1250 ML |
| 154 | For Antimicrobial Hand Washing,Surgical hand washing Body washing and showering. Chlorhexidine Gluconate Solution IP 20 Percent v/v(equivalent to Chlorhexidine Gluconate 4 Percent w/v)Passes EN 1499 Standards Selflife 2 years Pack Size 1250 Ml. |
| 155 | For Antimicrobial Hand Washing,Surgical hand washing Body washing and showering. Povidone-Iodine IP 7.5 Percent w/v(equivalent to 0.75 Percent w/v available Iodine)with Emollient & moisturiserPasses EN-1040 Standard Self Life 2 Years Pack size 500 ML. |
| 156 | Pre & post-surgical skin antisepsis. Chlorhexidine Gluconate Solution IP 2.5 Percent v/v(equivalent to Chlorhexidine Gluconate 0.5 Percent w/v)Ethanol IP 70 Percent v/v Passes EN-1040 Selflife 2 Years Packsize 500 ML |
| 157 | Treatment of bacterial or mycotic skin infection Povidone-Iodine IP 10 Percent w/v (1.0 Percent w/v available Iodine) U.S.P equivalent to 1 Percent available IodinePasses EN-1040 Selflife 2 years Pack size 500 ML. |
| 158 | Prophylactic casuality proceduresTreatment of bacterial or mycotic skin infection & Pre-surgical handwashing. Available Iodine 1 Percent w/v in an Aqueous <5 sodium Iodide, <1 surfactant base, <88 water Shelf Life of 5 YearsPasses EN-1040 Pack Size 500 ML |
| 159 | Cleaning and care of skin germicidal whole body washing. Octenidine based wash mitts with pratical hand dimension, tested as per European Norms containing octenidine HCL,aqua, glycerine, cocamidopropylamine oxide, sodium lactate, allantoin, ethylhexyl glycerine Selflife 1 year Pack size 10 Mitts Per Packet |
| 160 | Pre-Surgical and Post-Surgical Skin Antisepsis Chlorhexidine Gluconate Solution IP 10 Percent v/v (equivalent to Chlorhexidine Gluconate 2 Percent w/v) Isopropyl Alcohol IP 70 Percent v/vPasses EN 13727, EN 13624 and EN 14476 Standards Selflife 2 Years Pack Size 500 ML |
| 161 | Pre-Surgical and Post-Surgical Skin Antisepsis Chlorhexidine Gluconate Solution IP 10 Percent v/v (equivalent to Chlorhexidine Gluconate 2 Percent w/v) Ethanol IP 80 Percent v/v Selflife 2 Years Packsize 500 ML |
| 162 | Critical Area Fumigation Stabilized formulation of Hydrogen Peroxide 10 Percent v/vSilver 0.01 Percent w/v for critical area fumigation and surface disinfection, Non- toxic, Non-irritating, eco-friendly, 1 Litre Passes EN-1040 Selflife 2 years |
| 163 | Critical surface disinfection Each 100 g contains Didecyldimethyl Ammonium Chloride: 7.0 gCorrosion inhibitors, Fragrance, Excipients q.s. (alcohol free, aldehyde free) 2 years 10 months 500 ML |
| 164 | Emergency Disinfection Each 100 g contains Ethanol IP: 10.0 g2-propanol IP: 9.0 g/ isopropanol1-propanol: 6.0 g/ n-propanolprovided with convenient hand sprayer; Passes EN-1040 Pack Size 500 ML |
| 165 | Instant Disinfection of alcohol-compatible, high touchsurfaces in hospitalsIsopropyl Alcohol I.P. 70 Percent v/v, Surfactant, Corrosion Inhibitor,Stabilizer & Fragrance. Meets Latest NCDC and WHO GuidelinesPasses EN-1040 Selflife 3 Years Packsize 500 ML |
| 166 | High level Disinfection & Cleaning in One. 100 g of granules contain the following active ingredients: 43 g sodium per carbonate, 22 g tetraacetylethylenediamine.Passes EN 13624, EN 13727, EN 14348, EN 14561, EN 14562, EN 14563, EN 13704 and EN 14476 Standards Self life Inactivated Solution : 2 yearsActivated Solution: 1 day Pack Size1.5 kg Box |
| 167 | Sterilization Sal Reel 15cm x 200mt Iodine Test Pass. Should be have Indicator Strip on the same Pack Size 1 Reel |
| 168 | Sterilization Sal Reel 30cm x 200mt Iodine Test Pass. Should be have Indicator Strip on the same Pack Size 1 Reel |
| 169 | Sterilization Sal Reel 25cm x 200mt Iodine Test Pass. Should be have Indicator Strip on the same Pack Size 1 Reel |
| 170 | Sterilization Sal Reel 40cm x 200mt Iodine Test Pass. Should be have Indicator Strip on the same Pack Size 1 Reel |
| 171 | Ahlstrom 35 GSM Non Wovan With Hydro Head CM (limit 55 to 65) Trap Tear MD (limit 4500 to 5500) 100x100 cm (1/pic) |
| 172 | Ahlstrom 35 GSM Non Wovan With Hydro Head CM (limit 55 to 65) Trap Tear MD (limit 4500 to 5500) 120x120cm (1/pic) |
| 173 | 100 Percent Cotton made Doctor Apron with 2 Pockets on each side,half sleeve,made of 265 gsm cotton material |
| 174 | 60 Percent Cotton and 40 Percent Polyester made Doctor Scrub Shut for Male,'V' Neck, with one pocket on right hand side - size - small |
| 175 | 60 Percent Cotton and 40 Percent Polyester made Doctor Scrub Shirt for Male, 'V' Neck, With one pocket on right hand side - Size - Large |
| 176 | 60 Percent Cotton and 40 Percent Polyester made Doctor Scrub Shirt for Male, 'V' Neck, With one pocket on right hand side - Size - Extra Large |
| 177 | 60 Percent Cotton and 40 Percent Polyester made Doctor Scrub Shirt for Female, Narrow 'V' Neck, With one pocket on right hand side - Size - Small |
| 178 | 60 Percent Cotton and 40 Percent Polyester made Doctor Scrub Shirt for Female, Narrow 'V' Neck, With one pocket on right hand side - Size - Medium |
| 179 | 60 Percent Cotton and 40 Percent Polyester made Doctor Scrub Shirt for Female, Narrow 'V' Neck, With one pocket on right hand side - Size - Large |
| 180 | 60 Percent Cotton and 40 Percent Polyester made Doctor Scrub Shirt for Female, Narrow 'V' Neck, With one pocket on right hand side - Size - Extra Large |
| 181 | 60 Percent Cotton and 40 Percent Polyester made OT Gown with stockinet on wrist end, should be wrapping thread, Knee length |
| 182 | 30 Percent Cotton and 70 Percent Polyester made Patient Gown for Male, Should be in 2 Piece, Should be with White & Blue Vertical Stripes, With Elastic in lower |
| 183 | 30 Percent Cotton and 70 Percent Polyester made Patient Gown for Female, Should be in 1 Piece, Gown Type with thread for tie on back side, Should be with White & Pink Vertical Stripes, Should be with velcro on back side |
| 184 | 1x1 mtr Plain Drape for Surgery Room, Should be made up of 75 Percent Cotton & 25 Percent Polyester |
| 185 | 1.5x1.5 mtr Plain Drape for Surgery Room, Should be made up of 75 Percent Cotton & 25 Percent Polyester |
| 186 | 2x2 mtr Plain Drape for Surgery Room, Should be made up of 75 Percent Cotton & 25 Percent Polyester |
| 187 | 1x1 mtr Hole Drape for Surgery Room, Should be made up of 75 Percent Cotton & 25 Percent Polyester, Should have Hole on Incision site of at least 6\\"x6\\", Borders of Hole should be covered with Polypropylene material of 120gsm & Should be properly stitched |
| 188 | 1.5x1.5 mtr Hole Drape for Surgery Room, Should be made up of 75 Percent Cotton & 25 Percent Polyester, Should have Hole on Incision site of at least 9\\"x9\\", Borders of Hole should be covered with Polypropylene material of 120gsm & Should be properly stitched |
| 189 | 2x2 mtr Hole Drape for Surgery Room, Should be made up of 75 Percent Cotton & 25 Percent Polyester, Should have Hole on Incision site of at least 12\\"x12\\", Borders of Hole should be covered with Polypropylene material of 120gsm & Should be properly stitched |
| 190 | Manman BCDR Electrical Driving Unit 90W |
| 191 | Manman BCDR Electrical Drill Handpiece with Manman chuck 1200 |
| 192 | Manman Chuck Key 6 mm |
| 193 | Manman BCDR Electrical Reaming Handpiece AO Coupling 400 |
| 194 | Manman BCDR Electrical Pistol Grip Sagittal Saw Handpiece |
| 195 | Manman BCDR Electrical Sagittal Saw Blade Set (Set of 5) |
| 196 | Manman Intramedullary Guide Wire Set (Set of 3) |
| 197 | Manman Transfer Tube |
| 198 | Intercoastal Drainage BAG (Chest-Drain Bag) |
| 199 | Central Venous Catheter adult 3 lumen 7Fr & 16 cm length with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 200 | Central Venous Catheter adult 3 lumen 7Fr & 15 cm length with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 201 | Central Venous Catheter adult 3 lumen 7Fr & 13 cm length with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 202 | Central Venous Catheter 3Fr & 5cm Single lumen with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 203 | Central Venous Catheter 4Fr & 6cm/8cm Double lumen with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 204 | Central Venous Catheter 4.5 Fr & 6cm /8cm Double lumen with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 205 | Central Venous Catheter 5Fr & 8cm/ 10 cm Triple lumen with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 206 | Central Venous Catheter 5Fr & 8cm/10cm Triple lumen with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 207 | Central Venous Catheter 6Fr & 15cm Triple lumen with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 208 | Short Term Femoral Polyurithane Catheter with double lumen 11.5 Fr & 13 cm length, Soft PVC dilator for smooth insertion, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 209 | Short Term Jugular Polyurithane Catheter with double lumen 11.5 Fr & 13 cm length,Soft PVC dilator for smooth inserton, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 210 | Short Term Femoral Polyurithane Catheter with double lumen 12 Fr & 15 cm length, Soft PVC dilator for smooth insertion, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 211 | Short Term Jugular Polyurithane Catheter with double lumen 12 Fr & 15 cm length, Soft PVC dilator for smooth insertion,Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 212 | Short Term Femoral Polyurithane Catheter with triple lumen 12 Fr & 13 cm length, Soft PVC dilator for smooth insertion,Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 213 | Short Term Jugular Polyurithane Catheter with triple lumen 12 Fr & 13 cm length, Soft PVC dilator for smooth insertion, Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 214 | Short Term Femoral Polyurithane Catheter with triple lumen 12 Fr & 16 cm length, Soft PVC dilator for smooth insertion,Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 215 | Short Term Jugular Polyurithane Catheter with triple lumen 12 Fr & 16 cm length, Soft PVC dilator for smooth insertion,Non kinking guide wire made up of 45 Percent titanium & 55 Percent nickel, with CE,ISO & HTCert certified |
| 216 | Biosynthetic skin protective layer as substitute which designed for advanced wound healing and burn management, providing an effective antimicrobial barrier to protect the wound and burn site while maintaining optimal moisture by balancing fluid and Gas level for faster healing. It should be biocompatible, suitable for use on partial- and full-thickness wounds, and capable of remaining in place throughout the healing process and promoting smooth development of new skin , it should be CE certified and manufactured under ISO 13485-certified quality management system. Size: 8cm |
| 217 | A fully synthetic, biodegradable dermal regeneration dermal matri-/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 06-08cm |
| 218 | A fully synthetic, biodegradable dermal regeneration dermal matri-/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 10-10cm |
| 219 | A fully synthetic, biodegradable dermal regeneration dermal matri-/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 10-20cm |
| 220 | A fully synthetic, biodegradable dermal regeneration dermal matri-/Implant, 100 Percent synthetic, Non-collagenous and non-biological, bi-layer dermal substitute with Non-bio degradable transparent sealing membrane.enabling two-stage reconstruction with visual neodermis formation which suitable for full-thickness wounds including burns, trauma, diabetic and post-oncologic defects 20-40cm |
| 221 | Complete Trocar system 13 mm with working length of 110-120 mm with sterilizable silicone flap and fle-ible tip with pin holes near the tip for safety outlet of CO2- 1 no’s with shaft and tip sufficiently fle-ible to permit insertion of curved instruments and sufficiently firm to ensure access to the operation area-1 no’s Item Coated must be CE approved from EU notified body or USFDA Approved |
| 222 | 380-512 Mhz UHF split Band 16 channel analog Handheld |
| 223 | Castro- vijo scissors |
| 224 | Sprite Lamp |
| 225 | A.C.Maintenar |
| 226 | Autoclave label Roll 500 label |
| 227 | B.P. Cuff Medium, 1 Nos. |
| 228 | Bains circuit, 1 Nos. |
| 229 | Bowl S.S. Large, 1 Nos. |
| 230 | Bowl S.S. Small, 1 Nos. |
| 231 | Bowman's lacrimal probe 00 Size, 1 Nos. |
| 232 | Bowman's lacrimal probe 01-size , 1 Nos. |
| 233 | Bowman's lacrimal probe 2 size, 1 Nos. |
| 234 | BP(bardparker) Handle No.3 for knief holding |
| 235 | BP(bardparker) Handle No. 4 for knief holding |
| 236 | Castroviego scissiors 8\\" curved on flat Jewellers forcep 8\\" ISI CE certified |
| 237 | Castrovie's conjunctiva's scissor stainless steel , 1 Nos. |
| 238 | Cats Paw Retractor |
| 239 | Cautrey Boll point Stainless steel, 1 Nos. |
| 240 | Chalazion Clamp Stainless steel, 1 Nos. |
| 241 | Chemical indicator tape to monitor ETO sterilization by indicating a colour change of Yellow /Green to Red for easy identification of processed and unprocessed loads/ packs. Applicable to both warm and cool temperature cycles run at 37 degree C or >50 degree C. 3/4\\" x 55Mtr. Roll. |
| 242 | Cornea holder forcep round tipped ball point 8\\" Jewellers forcep 8\\" ISI CE certified |
| 243 | Corneal scissor small micro curved, 1 Nos. |
| 244 | Corneal scissors(paediatric) Stainless steel, 1 Nos. |
| 245 | Cornio scleral scissors small titanium, 1 Nos. |
| 246 | Curved small scissor R+ & L+ Stainless steel, 1 Nos. |
| 247 | Dastoor's superior rectus forceps(paediatric) Stainless steel, 1 Nos. |
| 248 | Dastoors's Superior rectus Holding forceps Stainless steel, 1 Nos. |
| 249 | Digital BP instrument ISI, 1 Nos., CE certified |
| 250 | Disposable corneal trephine 5.5mm. No.5.5, 1 Nos. |
| 251 | Disposable corneal trephine 5mm No. 5, 1 Nos. |
| 252 | Disposable corneal trephine 6.5mm. No.6.5, 1 Nos. |
| 253 | Disposable corneal trephine 6mm No.6, 1 Nos. |
| 254 | Disposable corneal trephine 7.5mm. No.7.5, 1 Nos. |
| 255 | Disposable corneal trephine 7mm. No.7, 1 Nos. |
| 256 | Disposable corneal trephine 8mm. No.8, 1 Nos. |
| 257 | Drape Plastic (100 cm X 80 cm) , 1 Nos. |
| 258 | Dress. Aborsbant cotton wool I.P. 500 gm (ISI MARK)500gm. Pac. |
| 259 | Dress. Aborsbant gauge (ISI Mark) 18 Mtr. x 60 cm Than1 Than. |
| 260 | Dress. Adhesive zinc tape u.s.p.10 cm x 10 mtr. cylinder of 3 roll1 Spool x 3 Roll. |
| 261 | Dress. Adhesive zinc tape u.s.p.5 cm x 10 mtr Cylinder of 6 roll1 Spool x 6 Roll. |
| 262 | Dress. Adhesive zinc tape u.s.p.7.5 cm x 10 mtr Cylinder of 4 roll1 Spool x 4 Roll. |
| 263 | Dress. Bandage Cloth (ISI Mark) 20 Mtr. x 100 cm Than1 Than. |
| 264 | Dress. Elastoplast Adhesive Bandage size 10 cm x 2.7 mtr. Pkt of 1 Roll, 1 Nos. |
| 265 | Drum Dressing SS 225 mm x 225 mm, 1 Nos. With ISI Mark |
| 266 | Drum Dressing SS 275 mm x 240 mm, 1 Nos. With ISI Mark |
| 267 | Drum Dressing SS 350 mm x 130 mm, 1 Nos. With ISI Mark |
| 268 | Drum Dressing SS 350 mm x 240 mm, 1 Nos. With ISI Mark |
| 269 | Dressing drum 6'' X 6\\" |
| 270 | Dressing drum 6'' X 10\\" |
| 271 | Dyna Plast, ISI certified |
| 272 | E.C.G. Electrodes Disposable , 1 Nos. |
| 273 | ECG Paper Roll Size 50 mm x 20 Mtr. Roll |
| 274 | Fine Scissor(4\\") ,Curved |
| 275 | Fine Scissor(4\\") ,Straight |
| 276 | Freers PERIOSTEUN Elevator |
| 277 | Kidney Tray S.S. 8\\" 10\\", 1 Nos., ISI mark |
| 278 | Kuglens lens manipulator Stainless steel, 1 Nos. |
| 279 | Kuglens lens manipulator Stainless steel, Ball type, 1 Nos. |
| 280 | Lim's forceps (paediatric) Stainless steel, 1 Nos. |
| 281 | Lim's Forceps Stainless steel, 1 Nos. |
| 282 | Surgical Rubber gloves with ISI Mark 4148-1989 with latest amendment size : 6'', 1 Pair. CECERTIFIED |
| 283 | Surgical Rubber gloves with ISI Mark 4148-1989 with latest amendment size : 6.½'', 1 Pair. CECERTIFIED |
| 284 | Surgical Rubber gloves with ISI Mark 4148-1989 with latest amendment size : 7'', 1 Pair. CECERTIFIED |
| 285 | Surgical Rubber gloves with ISI Mark 4148-1989 with latest amendment size : 7½'', 1 Pair. CECERTIFIED |
| 286 | Vannas scissors straight, 1 Nos. |
| 287 | (a)Lance tip 15 degree |
| 288 | (b)Crescent bevel up |
| 289 | (c)Keratome 2.8 mm bevel up |
| 290 | (d) Enlarger 5.2 mm bevel up |
| 291 | 1) GREEN Squint hook |
| 292 | 10x10cm Adh Eye Drapes presterile |
| 293 | 2) JAMESON Squint hook |
| 294 | 2ml Disposable syringe |
| 295 | 5ml Disposable syringe with Additional rubber capping |
| 296 | 6-0 Silk suture |
| 297 | ACIOL |
| 298 | adson-brown tissue forceps |
| 299 | Air injection canula 27 & 28 |
| 300 | Ala double hook with octagonal handle |
| 301 | Alligolw micro ear forcep |
| 302 | Anterior Chamber Intra Ocular Lens |
| 303 | Anterior chamber Maintainer |
| 304 | Antrum curett |
| 305 | Antrum grasping forceps |
| 306 | Antrum punch left side downward and forward cutting |
| 307 | Antrum punch right side downward and forward cutting |
| 308 | AUFRICHT nasal retractor |
| 309 | B.P. Blade No.11 |
| 310 | B.P. Blade No.15 |
| 311 | Ball point cautery |
| 312 | Bard Parker handle no 3&4 |
| 313 | BELLUCCI scissor |
| 314 | BENJAMIN-LINDHOLM operating laryngoscope for newborn baby and infants |
| 315 | BIPOLAR coagulating forceps |
| 316 | blade no 11 |
| 317 | blade no 15 |
| 318 | blade non-sterile package of 100 |
| 319 | BRINER bipolar suction cannula |
| 320 | Capsular Polisher |
| 321 | Capsular tension ring No. 11 & 13 |
| 322 | Capsulorhexis forceps |
| 323 | Capsulotomy scissors |
| 324 | Castrovijo caliper - Straight, Curved |
| 325 | Cat's Paw Retractor |
| 326 | CAUTERY PENCIL BIPOLAR |
| 327 | CAUTERY PENCIL MONOPOLAR HAND SEITCH |
| 328 | Chalazion clamp |
| 329 | Chalazion scoop |
| 330 | Corneal scissors –Castroviejo |
| 331 | COTTLE crossbar osteotome straight |
| 332 | cottle bone cutter |
| 333 | COTTLE chisel |
| 334 | cottle chisel flat width 4mm |
| 335 | COTTLE columella clamp length 11cm |
| 336 | COTTLE crossbar osteotme curved |
| 337 | cottle crossbar osteotme, graduated straight |
| 338 | cottle elevator double ended |
| 339 | cottle lower lateral forceps |
| 340 | COTTLE metal mallet |
| 341 | cottle nasal knife |
| 342 | COTTLE nasal speculum |
| 343 | COTTLE retractor |
| 344 | cottle retractor, 2 prongs, blunt probe on left |
| 345 | cottle retractor, 2 prongs, blunt probe on right |
| 346 | cottle retractor, double ended |
| 347 | COTTLE scissor ,curved,length 10.5 cm |
| 348 | COTTLE scissors ,curved,length 10.5 cm |
| 349 | cotton applicators |
| 350 | CRAIG septum forceps |
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