Tender For Scardiothoracic Implants Ii , Silk 1 No 75Cm , Silk 1-0 R.C 75Cm , Silk 3-0 R.B. 75Cm , Silk 4-0 R.C. 75Cm , Silk 4-0 R.B. 75Cm , Umblical Tape 75Cm , Pacing Wire 2-0 18 Mm 75Cm , Pacing Wire 2-0 26 Mm 75Cm , Surgical Steel 4 No Cutting 48Mm ,, Jodhpur-Rajasthan

TDR : 54712235

Tender Notice
BOQ

11 Days Left

Jodhpur , Rajasthan

Tender Brief : Tender For Scardiothoracic Implants Ii , Silk 1 No 75Cm , Silk 1-0 R.C 75Cm , Silk 3-0 R.B. 75Cm , Silk 4-0 R.C. 75Cm , Silk 4-0 R.B. 75Cm , Umblical Tape 75Cm , Pacing Wire 2-0 18 Mm 75Cm , Pacing Wire 2-0 26 Mm 75Cm , Surgical Steel 4 No Cutting 48Mm ,

Document Fees
₹ 3500 /-

EMD
₹ 1200000.0 /-

Tender Value
₹ 6 Crore /-

Submission Date
07-04-2026

Competition Type
Indian

Bidding Type
Goods

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1	Silk 1 no 75cm
2	silk 1-0 R.C 75cm
3	Silk 3-0 R.B. 75cm
4	Silk 4-0 R.C. 75cm
5	Silk 4-0 R.B. 75cm
6	Umblical Tape 75cm
7	Pacing wire 2-0 18 mm 75cm
8	Pacing wire 2-0 26 mm 75cm
9	Surgical steel 4 no cutting 48mm
10	Surgical steel 4 no Blunt point R.B. 45MM
11	Surgical steel 5 no cutting 48 mm
12	Surgical steel 5 no Blunt point R.B. 45 mm
13	Surgical steel 6 no cutting 48 mm
14	Surgical steel 6 no Blunt point 45 mm
15	Polyester 2-0 10x75cm 17.5 mm
16	Polyester 2-0 10x75cm 17.5 mm 3x3x1.0 pledget
17	Polyester 2-0 10x75cm 26mm
18	Polyester 2-0 10x75cm 26mm 6x3x1.0 Pledget
19	Polyester 2-0 10x75cm 26mm 3x3x1.5 Pledget
20	Polyester 2-0 10x75cm 26mm 3x3x1.0 Pledget
21	Polyproplyne 2-0 17.5 mm D.A. 90 CM
22	Polyproplyne 2-0 17.5 mm D.A. 150 CM
23	Polyproplyne 2-0 26 mm D.A. 90 CM
24	Polyproplyne 2-0 26 mm D.A. 150 CM
25	Polyproplyne 3-0 17.5 mm D.A. 90 CM
26	Polyproplyne 3-0 25 mm D.A. 90 CM
27	Polyproplyne 3-0 26 MM D.A. 90 cm
28	Polyproplyne 4-0 13 MM D.A. 60 cm
29	Polyproplyne 4-0 16 MM D.A. 90 cm
30	Polyproplyne 4-0 17.5 mm D.A. 90 cm
31	Polyproplyne 4-0 17.5 mm D.A. 90 cm Pledget 3x3x1.5
32	Polyproplyne 4-0 20 mm D.A. 90 cm
33	Polyproplyne 4-0 26 mm D.A. 90 cm
34	Polyproplyne 4-0 26 mm D.A. 90 cm Pledget 3x3x.50
35	Polyproplyne 5-0 10 mm D.A. 60 cm
36	Polyproplyne 5-0 10 mm D.A. 75 cm
37	Polyproplyne 5-0 10 mm D.A. 60 cm Pledget 3x3x1.5
38	Polyproplyne 5-0 10 mm D.A. 75 cm Pledget 3x3x1.5
39	Polyproplyne 5-0 10 mm D.A. 75 cm Pledget 3x3x0.5
40	Polyproplyne 5-0 13 MM D.A. 60 cm pledget 3x3x1.5
41	Polyproplyne 5-0 13 MM D.A. 60 cm pledget 3x3x0.5
42	Polyproplyne 5-0 13 MM D.A. 75 cm pledget 3x3x0.5
43	Polyproplyne 5-0 13 MM D.A. 45 cm
44	Polyproplyne 5-0 13 MM D.A. 75 cm
45	Polyproplyne 5-0 16 MM D.A. 90 cm
46	Polyproplyne 5-0 16 MM D.A. 90 cm Pledget 3x3x1.5
47	Polyproplyne 5-0 20 MM D.A. 90 cm
48	Polyproplyne 6-0 10 MM D.A. 60 cm
49	Polyproplyne 6-0 10 MM D.A. 75 cm
50	Polyproplyne 6-0 10 MM D.A. 60 cm 3X3X1.5
51	Polyproplyne 6-0 10 MM D.A. 60 cm 3X3X0.5
52	Polyproplyne 6-0 13 MM D.A. 60 cm
53	Polyproplyne 6-0 13 MM D.A. 60 cm Black Needle
54	Polyproplyne 6-0 13 MM D.A. 45 cm
55	Polyproplyne 6-0 13 MM D.A. 75 cm
56	Polyproplyne 6-0 13 MM D.A. 90 cm
57	Polyproplyne 6-0 11 MM D.A. 60 cm
58	Polyproplyne 6-0 9 MM D.A. 60 cm
59	Polyproplyne 6-0 9 MM D.A. 75cm
60	Polyproplyne 7-0 9MM D.A. 60cm
61	Polyproplyne 7-0 9MM D.A. 75cm
62	Polyproplyne 7-0 9MM D.A. 60cm Black
63	Polyproplyne 7-0 9MM D.A. 60cm P V Needle
64	Polyproplyne 7-0 9MM D.A. 60cm C C Needle
65	Polyproplyne 7-0 10MM D.A. 60cm
66	Polyproplyne 7-0 8MM D.A. 60cm cc needdle
67	Polyproplyne 7-0 8MM D.A. 60cm P V Needle
68	Polyproplyne 7-0 8MM D.A. 60cm Black
69	Polyproplyne 8-0 6 MM D.A.60 cm
70	Polyproplyne 8-0 6.5 MM D.A.60 cm
71	Polyproplyne 8-0 9 MM D.A.60 cm
72	Polyproplyne 8-0 10 MM D.A.60 cm
73	Polyglactin 1 no R.B. 40 mm A.M. 90 cm
74	Polyglactin 1 no R.B. 40 mm A.M. 70 cm
75	Polyglactin 1 no R.B. 36 mm A.M. 120 cm
76	Polyglactin 1 no R.B. 36 mm A.M. 90 cm
77	Polyglactin 1 no.R.C. 40MM A.M. 90 cm
78	Polyglactin 1 no.Taper cut 40MM A.M. 90 cm
79	Polyglactin 1-0 no. R.B. 40MM A.M. 90 cm
80	Polyglactin 1-0 no.Taper cut 36MM A.M. 90 cm
81	Polyglactin 1-0 no.R.C. 36MM A.M. 90 cm
82	Polyglactin 1-0 no R.B. 30 mm A.M. 90 cm
83	Polyglactin 1-0 no R.B. 36 mm A.M. 90 cm
84	Polyglactin 2-0 R.B. 30 mm A.M. 90 CM
85	Polyglactin 2-0 R.B. 30 mm A.M. 70 CM
86	Polyglactin 2-0 R.B. 40 mm A.M. 90 CM
87	Polyglactin 2-0 R.C. 40 mm A.M. 90 CM
88	Polyglactin 2-0 R.B. 36 mm A.M. 90 CM
89	Polyglactin 3-0 R.C. 24 mm A.M. 70 CM
90	Polyglactin 3-0 R.B. 20 mm A.M. 90 CM
91	Polyglactin 4-0 R.B. 20 mm A.M. 70 CM
92	Polyglactin 5-0 R.B. 16 mm A.M. 45 CM
93	PGLA910 VIO 70CM 3-0 X 20MM 1/2 CIR TP
94	PGLA910 + VIO 90CM 2-0 X 30MM 1/2 CIR TP
95	POLYAMIDE BLK 70CM 2-0 X 45MM 3/8 CIR RC
96	POLY.P BLUE 90 CM 3-0 X 26MM 1/2 CIR TP DA CV
97	POLYAMIDE BLK 70CM 3-0 X 26MM 3/8 CIR RC
98	PGLA910 VIO 90CM 1X 40MM 1/2 CIR TIP HV
99	PDS VIO 150CM 1 X 50MM 1/2 CIR TP LP HV
100	PDS VIO 70CM 4-0 X 20MM 1/2 CIR TP LTP
101	PDS VIO 75CM 3-0 X 20MM 1/2 CIR TP DA
102	PDS VIO 90CM 1 X 40MM 1/2 CIR TP HV
103	POLY.P BLUE 70CM 2-0 X 30MM 1/2 CIR TP
104	POLY.P BLUE 70CM 0 X 30MM 1/2 CIR TP
105	POLY.P BLUE 70CM 0 X 30MM 1/2 CIR TP
106	POLY.P BLUE 70CM 1 X 40MM 1/2 CIR TP HV
107	POLY.P BLUE 90CM 2-0 X 30MM 1/2 CIR TP
108	POLY.P BLUE 90CM 4-0 X 25MM 1/2 CIR TC DA CV
109	POLY.P BLUE 90CM 0 X 30MM 1/2 CIR TP
110	POLY.P BLUE 90CM 0 X 30MM 1/2 CIR TP
111	POLY.P BLUE 70CM 4-0 X 16MM 1/2 CIR TP CV
112	POLY.P BLUE 70CM 3-0 X 25MM 1/2 CIR TP
113	POLY.P BLUE 70CM 1 X 30MM 1/2 CIR TP HV
114	POLY.P BLUE 70CM 1 X 30MM 1/2 CIR TP HV
115	POLY.P BLUE 75 CM 6-0 X 9MM 3/8 CIR TP DA CV
116	GUT CRMC 50CM 1 pre knot loop
117	PGLA910 VIO 90CM 1 X 40MM 1/2 CIR RC HV
118	PGLA910 VIO 90CM 2-0 X 40MM 1/2 CIR RC
119	PGLA910 VIO 35CM 1 X 23MM 1/2 CIR RC HV
120	PDS 1 no Loop
121	Absorbable Tacker
122	Absorbable tacker 30
123	Absorbable Tacker 20
124	Barb Sutures Polydiaxone 1-0 RB
125	Barb Sutures Poluglecaprone /Polyglactin 2-0
126	Barb sutures Polydiaxone 2-0
127	Barb(Polydiaxonone Violet) 30 cm 1-0 1/2 C.R.B.
128	Barb(Polydiaxonone Violet) 15 cm 1-0 1/2 C.R.B.
129	Barb(Polydiaxonone Violet) 30cm 1-0 1/2 C.R.B.
130	Barb(Polydiaxonone Violet) 45cm 1-0 1/2 C.R.B.
131	Barb(Polydiaxonone Violet) 45cm 2-0 1/2 C.R.B.
132	Barb(Polydiaxonone Violet) 45cm 2-0 1/2 C.R.B.
133	Barb(Polydiaxonone Violet) 25 cm 2-0 1/2 C.R.B.
134	Barb(Polydiaxonone Violet) 45cm 3-0 3/8 C. R.C.
135	Barb(Polydiaxonone Violet) 15 cm 3-0 1/2 C.R.B.
136	Barb(PGA-PCL UND) 36 cm 2-0
137	Barb(Polydiaxonone Violet) 30 cm 1-0
138	Barb(PGA-PCL UND) 30 cm 3-0
139	Barb(PGA-PCL UND) 30 cm 4-0
140	2 ml Fibrin sealant with synthetic Aprotinin 2ml Glu Dual tip syringe system and vialswith sterile water for reconstitution should be part of the package.
141	4ml Fibrin sealant with synthetic Aprotinin 4ml Glu Dual tip syringe system and vialswith sterile water for reconstitution should be part of the package.
142	10ml Fibrin sealant with synthetic Aprotinin 10 ml· Dual tip syringe system and vialswith sterile water for reconstitution should be part of the package.
143	5 ml Hemostatic matrix with thrombin 5 ml . Pre-filled syringe of Bovine-derivedSpherical Gelatin granule matrix along with a vial of human-derived Thrombin component (500IU/ml) & 0.9% Sodium Chloride
144	10 ml Hemostatic matrix with thrombin 10 ml. Pre-filled syringe of Bovine-derivedSpherical Gelatin granule matrix along with a vial of human-derived Thrombin component (500IU/ml) & 0.9% Sodium Chloride
145	Resorbable Collagen based Sealing Hemostat- Material of Construction: Bovine Collagenpatch, NHS-PEG 27mm * 27 mm
146	Resorbable Collagen based Sealing Hemostat- Material of Construction: Bovine Collagenpatch, NHS-PEG 45mm * 45 mm
147	Resorbable Collagen based Sealing Hemostat- Material of Construction: Bovine Collagenpatch, NHS-PEG : 45mm * 90 mm
148	Calcium free(BSS) Balanced Salt Solutions in non PVC Bag 500 ml for Infusion 500ml flexible bags; Osmolarity – 295 mOsm/l; Sodium Chloride - 5.26/l; Sodium Gluconate - 5.02/l; Sodium Acetate - 3.68g/l; Potassium Chloride - 0.37g/l; Magnesium Chloride -0.30g/l
149	TPN 1Ltr Peripheral (3 in one) for Periperal IV Emlusions 1000ml-1200ml with 80% Olive/20% Soya Lipid,Amino acids,glucose & Electrolytes. should contain Protein 20-45 gm/L Lipid 20-40gm/L Glucose 80-160 gm/L
150	TPN 1Ltr Central (3 in one) for Central IV Emlusions 1000ml-1200ml with 80% Olive/20% Soya Lipid,Amino acids,glucose & Electrolytes. should contain Protein 20-45 gm/L Lipid 20-40gm/L Glucose 80-160 gm/L
151	Sensors for Bio Reactance non invasive monitor
152	Small size garments for vest airway machine
153	Medium size garments for vest airway machine
154	Large size garmets for Vest airway machine
155	Elastomeric Pumps are non-electronic medication pumps ambulatory infusion therapy. Portable Elastomeric pump (single use) Fixed rate infusion 2ml/Hour , 130 ml fill volume,5-micron filter with non-kinking tube and blue winged cap .
156	Elastomeric Pumps are non-electronic medication pumps ambulatory infusion therapy. Portable Elastomeric pump (single use) Fixed rate infusion 5ml/Hour , 300 ml fill volume,5-micron filter with non-kinking tube and blue winged cap .
157	Elastomeric Pumps are non-electronic medication pumps ambulatory infusion therapy. Portable Elastomeric pump (single use) multivirate infusion LV 2-3-5ml/Hour , 300 ml fill volume,5-micron filter with non-kinking tube and blue winged cap .
158	Elastomeric Pumps are non-electronic medication pumps ambulatory infusion therapy. Portable Elastomeric pump (single use) multivirate infusion LV 5/7/12ml/Hour , 300 ml fill volume,5-micron filter with non-kinking tube and blue winged cap .
159	PLP Chemoport with titanium internal chamber with silicone catheter 8 Fr-8.5 Fr
160	A sterile translucent adhesion barrier membrane composed of sodium hyaluronate andcarboxymethyl cellulose full sheet 13x15 cm
161	A sterile translucent adhesion barrier membrane composed of sodium hyaluronate andcarboxymethyl cellulose full sheet 13x7.5 cm
162	Vac Dressing Medium NPWT Polyurethene foam dressingwith drape.Ruler. Sensatrac Technology Trac tubing.1 Ltr cainester for exudate collection.DGCI, FDA and CE certified. Company having manufacturing and import License. Compatible to existing machine
163	Vac Dressing Large NPWT Polyurethene foam dressingwith drape.Ruler. Sensatrac Technology Trac tubing.1 Ltr cainester for exudate collection.DGCI, FDA and CE certified. Company having manufacturing and import License. Compatible to existing machine
164	Cainester 500 ML. compatible to existing machine.
165	Human UC Dressing Allograft Strile Dehydrated human umblical cord derived membraneAllograft 5 cm x 3 cm
166	Human amniotic Allograft strile Dehydrated human amnion chorion menbrane withpolyhexamethylene biguanide 11 cm x 7 cm
167	Human amnion chorion with PHMB Powder strile dehydrated human amnion chorionand polyhexamethylene biguanide powder 3 gm 10 ML
168	Human amniotic allograft strile dehydrated human amnion chorion membrane withpolyhexamethylene biguanide 7 cm x 7 cm
169	Sterile Collagen sheets in meshed form. Pure Type 1&3 triple helical Membrane Bovine Origin preserved in a mixture of Iso Propyl alcohol and water Gamma sterilized and supplied in double sterile pouches. Biocompatible as per ISO 9001/ ISO13485 n10x10
170	Sterile Collagen sheets in Dry form. Pure Type 1&3 triple helical Membrane BovineOrigin Gamma sterilized and supplied in double sterile pouches. Biocompatible as per ISO 9001/ ISO13485 n 10x10
171	Sterile Collagen sheets in Dry form. Pure Type 1&3 triple helical Membrane BovineOrigin Gamma sterilized and supplied in double sterile pouches. Biocompatible as per ISO 9001/ ISO13485 n 10x20
172	Silicone sheet Pure Poly Siloxane based silicone scar management product in sheetform. 10x10
173	Biofil AB Sterils medicated collegan Particles 5 ML
174	Biofil AB Sterils medicated collegan Particles 10 ML
175	Urgotul Ag Silver 10x12 Lipido-Colloid technology contact layer impregnated with silver salts contact layer consists of silver healing Matrix made of polyester mesh impregnated with hydrocolloid particles( CMC) ,petroleum jelly, polymers and silver salts
176	Urgotul Ag Silver 15x20 Lipido-Colloid technology contact layer impregnated with silver salts contact layer consists of silver healing Matrix made of polyester mesh impregnated with hydrocolloid particles( CMC) ,petroleum jelly, polymers and silver salts
177	Urgotul Ag Silver 20x40 Lipido-Colloid technology contact layer impregnated with silver salts contact layer consists of silver healing Matrix made of polyester mesh impregnated with hydrocolloid particles( CMC) ,petroleum jelly, polymers and silver salts
178	Urgotul Border 8x8 Lipido-Colloid trechnology foam dressing with adhesive border self - adherent patented TLC matrixwound contact layer combined with absorbent polyurethane foam pad , a superabsorbent layer ,a vapour permeable waterproof outerfilm with soft silicone adhesive border
179	Urgotul Border 13x13 Lipido-Colloid trechnology foam dressing with adhesive border self -adherent patented TLC matrixwound contact layer combined with absorbent polyurethane foam pad , a superabsorbent layer ,a vapour permeable waterproof outerfilm with soft silicone adhesive border
180	Urgotul Border 20x20 Lipido-Colloid trechnology foam dressing with adhesive border self -adherent patented TLC matrixwound contact layer combined with absorbent polyurethane foam pad , a superabsorbent layer ,a vapour permeable waterproof outerfilm with soft silicone adhesive border
181	Urgotul Clean Ag 10x10 absorbent pad made of polyabsorbent fibres with an acrylic core, coated with a soft adherent healing matrix impregnated with silver (TLC-Ag: Technology Lipido-Colloid, composed of carboxymethyl cellulose particles, lipophilicsubstances and silver salts)
182	Urgotul Clean Ag 15x20 absorbent pad made of polyabsorbent fibres with an acrylic core, coated with a soft adherent healing matrix impregnated with silver (TLC-Ag: Technology Lipido-Colloid, composed of carboxymethyl cellulose particles, lipophilicsubstances and silver salts)
183	Transperint dressing with absorbant Pad fully transprent backing, hypoallergenic acrylicadhesive 5x7 cm.
184	Transperint dressing with absorbant Pad fully transprent backing, hypoallergenic acrylicadhesive 6x10 cm.
185	Transperint dressing with absorbant Pad fully transprent backing, hypoallergenic acrylicadhesive 9x25 cm.
186	Polyurethane film peripheral IV dressing for pediatric reinforced with soft cloth border and notch with pattern coated acrylic adhesive. It has a picture frame delivery system with 3 extra sterile tape strips for additional secural and and complies. Size: Size: 5cm x6cm.
187	Ventilator circuit 2 water trap with MDI Adoptor Plain. MD/5 Approved
188	Ventilator circuit with MDI Adoptor Single water trap. MD/5 Approved
189	Bain circuit Adult with tubing. MD/5 Approved
190	Bain circuit Pediatric with tubing. MD/5 Approved
191	DLT all Sizes
192	Pur-Xro 28G/1fr PICC catheter 1261.203 20cm length with stylet, spliting introducerneedle,securing wings, measuring tape and every cm marking , flow rate 0.7ml/min with 8 cm extension tubing and clamp
193	Pur-Xro 24G/2fr PICC detachable catheter 1284 30cm length with every cm marking , peelapart cannula, measuring tape and 10cm extention tube(flow rate 4.5ml/min.
194	Pur-xro 22G catheter 1212 with stight guidwire and introducer with integral extensionand clamp . Length 4,6,8,10,20cm
195	Radiopaqe wit EXPERT Technology, Contaning AgION™ antimicrobial agent CATHETER 40CM WITH 3.5, 4,5,8 FR COMPATIBLE FOR BOTH ARTERIAL AND VENUS ROUTE WITH FEMALE LUERLOCK SUPPLIED WITH STOPCOCK AND COLOUR CODED CLIP
196	XRO ICD Trocar drain with catheter for Pleural drainage of newborn Size 8Fr and 10 Fr.
197	Ultrasound guided Nerve stimulation needle with transparent hub and 50cm detachableextension.
198	Dialyzer with Tubing 1.4 Single use With Steam sterlization. Filter and Tubing Shouldbe same manufacterur
199	Dry Bicarbonate Bag 650 Gm Bibag. Compatible with fresenius Machine.
200	Citrosteril 5 Ltr Each 100 gm citro should have 21 gm citric acid. 1- hydrate lactic acid and malic acid.ph value in between 1.7 to 2.0 and have excellent removal oflimescaleand have disinfection and decalcification in one process.
201	Diasafe
202	Femoral Introducer sheath 4, 5, 6, 7, 8, 9, 10, 11 Fr with punture needle. Hydrophillic coated.11 cm Long. 18 G x 7 cm Long needle. 0.032 to 0.038 guide wire compatible. Cross cut valve to prevent back leak and air aspiration.Integral side port 3 way stopcock..suture eyefor securing sheath.Kink resistantdialator hub Lock mechanism
203	Radial Introducer sheath 4, 5, 6, 7, 8, 9, 10, 11 Fr with punture needle. Hydrophillic coated.11 cm Long. 18 G x 7 cm Long needle. 0.032 to 0.038 guide wire compatible. Cross cut valve to prevent back leak and air aspiration.Integral side port 3 way stopcock..suture eyefor securing sheath.Kink resistantdialator hub Lock mechanism
204	Femoral Introducer sheath 7 and 8 fr with punture needle. Hydrophillic coated. up to 75 cm Long. 18 G x 7 cm Long needle. 0.032 to 0.038 guide wire compatible. Cross cut valve to prevent back leak and air aspiration.Integral side port 3 way stopcock..suture eyefor securing sheath.Kink resistantdialator hub Lock mechanism
205	Femoral Introducer sheath 7 and 8 fr with punture needle. Hydrophillic coated. up to 95 cm Long. 18 G x 7 cm Long needle. 0.032 to 0.038 guide wire compatible. Cross cut valve to prevent back leak and air aspiration.Integral side port 3 way stopcock..suture eyefor securing sheath.Kink resistantdialator hub Lock mechanism
206	Hydrophilic coated Guide wire 260 cm Exchange Length.Should available in 0.025, 0.032, 0.035, 0.038. Angled and Straight Tip. Fixed and movable core CE certified
207	Hydrophilic coated Guide wire 150 cm .Should available in 0.025, 0.032, 0.035, 0.038.Angled and Straight Tip. Fixed and movable core CE certified
208	PTFE Guide wire 260 cm Exchange Length Extra stiff (Amplatzer type).Should available in 0.025, 0.032, 0.035, 0.038. Angled and Straight Tip. Fixed and movable core CE certified
209	ACT Crtidge Compatable with existing machine (medtronic)
210	Snare Adult
211	Snare
212	Catheter MPA
213	catheter MA
214	Catheter Pigtail
215	Angioseal
216	Diagnostic Tiger cath
217	Diagnostic Tiger cath
218	Flexible Digital uretero renoscope sleek. Digital CMOS imager chip on tip tech. 0°view. Field view 110°.depth of field 2mm-50mm+working length 650 to 670mm.working channel 3.3 fr or more. Compatible with laser Lithotripsy. Sterad sterlizatio method.
219	Digital semi rigid ureterorenoscope Ace. Digital CMOS imager chip on tip tech.6° view. Field view 110°. .depth of field 2mm-50mm+working length 400 to 450mm.working channel 3.5 fr or more. Compatible with laser Lithotripsy. Sterad sterlizatio method.
220	Flexible Digital cystonephroscope CN+S. Digital CMOS imager chip on tip tech. 0°view. Field view 110°.depth of field 2mm-50mm+working length 380mm.working channel 2 MM or more. Compatible with laser Lithotripsy. Sterad sterlizatio method.
221	Valvoplasty balloon catheters size 10-22 mm nominal pressure < 4 ATM
222	Balloon in Balloon BIB Catheters USFDA
223	Z Med type Balloon for Aortic Coarctation
224	CP stent uncovered Without Balloon Mounted 8zig
225	CP stent uncovered Without Balloon Mounted 10zig
226	CP stent uncovered With Balloon Mounted 8zig
227	CP stent uncovered With Balloon Mounted 10zig
228	CP stent covered Without Balloon Mounted 8zig
229	CP stent covered Without Balloon Mounted 10zig
230	CP stent covered With Balloon Mounted 8zig
231	CP stent covered With Balloon Mounted 10zig
232	Long sheath
233	Devil sheath
234	Mechanical Rotatable Heart Valves for both Aortic and Mitral Heart position available in sizes 17 mm to 33mm. Bi-leaflet and rotatable. protrusion of leaflets from the housing is 3.4mm.wall clearance – 6.6mm 85°. U.S FDA approved.Pyrolytic carbon. Patentedbutterfly upstream pivot design
235	Aortic Tissue Bioprosthetic Biological heart valves for Aortic Heart position available in sizes 19mm-27mm. Good Fluroscopic visibility. VIV ready future intervention. Triple composite porcine . Anti-calcification treatment Linx AC Technology. Lowest profile 9mm. U.S FDA approved.Low Pressure glutarldehyde fixation. Polyester ring.Reduceleaflet stress.
236	Mitral Tissue Bioprosthetic Biological heart valves for Mitral Heart position available in sizes 25mm-33mm. Triple composite porcine valves. Anti-calcification treatment Linx Technology. U.S FDA approved.Low Pressure glutarldehyde fixation. Good fluoroscope visibility.VIV ready future intervention.Lowest profile 9mm.Polyester ring.Ratcheting system.Scalloped inflow surface.
237	Annuloplasty Tricuspid Ring TARP Available in sizes 25mm to 35mm. tricuspid and mitral repair. double velour cuff . Full flexible ring can be tailored.Posterior support.Flexible design.Secure ergonomic holder and handle.Open holder facilitates.US. FDA approved
238	Mitral semi-Rigid SARP Ring has three-dimensional Flexibility. preserve the physiologic movement of the valve annulus.Sewing ring fabric: Polyester Double Velour.Core: Polyethylene.sizes 24mm-40mm. Secure ergonomic holder and handle quickly attach and detach to save time during implant.Solid, one-piece inner core resists needle penetration and reduces the potential for suturing through the core.USFDA
239	mitral Rigid RASR Ring Repair solutions available in both flexible as well as rigid forms. rigid ring is a full 3D ring which creates natural saddle shape. titanium alloy core.polyester cuff..unique triangular core.U.S FDA approved rings.sizes 22mm to34mm.
240	Conduit Double-velour woven fabric offers excellent sealing handling and healing characteristics.Collagen impregnation provides uniform tissue in-growth and biocompatibility. Rotatable valve attached. Cuff Configuration. US. FDA approved.sizes:19mm to 33 mm
241	Vessel harvesting system
242	The Endoscopic Harvesting System should be designed for use in conjunction with the 7mm Endoscope. Harvesting Cannula should havefour lumens to house the Endoscope, C-Ring, Distal Lens Washer Tube & BiSECTOR Bipolar Ligating Forceps for ligation & division of vessel branches.C-Ring/Distal lens washer should be independently controlled by a C-BiSECTOR can be extended/retracted through the main cannula by inserting it into the Tool Adapter Port, and rotated independently.Bipolar coagulation should be achieved using electrosurgical energy.Short Port Blunt Tip Trocar (BTT) should be provided which is used toprovide a port of access for insertion of endoscopic instruments into an incision site.syringe should be provided for inflation/deflation of the Balloon.
243	Silver knitted acetate collagen-coated polyester graft. Knitted, Woven.antimicrobial.reduce the risk of graft-related infection Silver acetate does not promote bacterial resistance Validated intended use with rifampicin loading.bovine collagen.Water permeability ≤ 5ml • cm-2 • min-1@120 mmHg Sizes 40 CM 6,7,8,10,
244	Silver knitted acetate collagen-coated polyester graft. Knitted, Woven.antimicrobial.reduce the risk of graft-related infection Silver acetate does not promote bacterial resistance Validated intended use with rifampicin loading.bovine collagen.Water permeability ≤ 5ml • cm-2 • min-1@120 mmHg Sizes 70 CM 6,7,8,10,
245	Silver Knitted Bifurgated acetate collagen-coated polyester graft. Knitted, Woven.antimicrobial.reduce the risk of graft-related infection Silver acetate does not promote bacterial resistance Validated intended use with rifampicin loading.bovine collagen.Water permeability ≤ 5ml • cm-2 • min-1@120 mmHg Sizes 50 cm 12x6, 14x7,16x8, 18x9
246	Heart Stablizer Thin mount with a constant low profile design for an optimized work area.Stabilizer allows a vertical drop of the FLEXLINK arm into the chest cavity.Proprietary technology provides 180º side-to-side range of motion of the arm.Integrated channels secure tubing away from the work area
247	Hearrt Positioner Active suspension technology allows normal cardiac motion and maintains stable hemodynamics.Tissue-conforming suction cup uses gentle vacuum to securely lift and hold the heart.Designed for apical or nonapical placement
248	Oxynator 1.5 Ltr
249	Oxynator 4 Ltr
250	Hemofilter Adult
251	Hemofilter Ped.
252	CABG KIT ON PUMP annexure 1
253	Double Valve Surgery Kit annexure 2
254	Toff Surgery Kit annexure 3
255	LB St. & LB Bifurgated The World only dilatation resistant ,gelatin sealed , Koper knitted polyester vascular graft. dramatically reduced dilatation , superb handling , unique rifampicin ionic bonding options , comprehensive range includes supported design .Gelsoft Plus
256	LB Bifurgateed bifurcate grafts has unique hydrolysable gelatin inpregnation , proventwillweave base fabric , superb handling , Excellent suture retention , Cardiothoracic and abdominal aplications . Gelweave
257	LB St. grafts has unique hydrolysable gelatin inpregnation , proven twillweave base fabric, superb handling , Excellent suture retention , Cardiothoracic and abdominal aplications. Gelweave St
258	Branch Design ,Aortic Arch graft Antegrade flow made easy by the perfusion side branch may offer 1) reduced incident of temporary neurological deficits , preventive effect against embolic stroke , potential for reduced operating time . Gelweave Plexus (4Branches)
259	Frozen Elephent trunk Gelatin Coating to achieve hemostasis & prevent ozzing, Antegrade Perfusion Branch, shorter circulatory time, -Ring Stent for better conformability to angulated descending Aorta, - Sienna Collar to achieve distal anstomosis, Plexus braches separtely for supra aortic vessel anastomosis, Delivery System- Ineer Melleable shaft allow to suit for different anatomy,- Guide wire Port to ensure the True Lumen insertion for dissection, - Short Handle to allow better visualization of Operation field. Thoraflex Hybrid.
260	Venous Sinus self expanding nitinol stent. Hybrid designfor radial force with high flexibility.electro polishing.radiopaque marker.Anti jump technique.braided sheath and flexible tip.rounded edges.independent ring system.high vessel wall.flash link.open cell design.Introducer 10Fr. Guide wire 0.035\\". 10,,12, 14, 16, 18, MM 60/80/120/150 MM.100 cm
261	Venous Sinus XL self expanding nitinol stent. use in IVC, SVC, and Aorta. close cell design.High radial strength.Tantalum marker .Anti jump technique.Radiopaque marker.braided sheath and flexible tip.0.035\\". 14 & 16mm stent should have 6F profile. 18mm and above stent should have 10 F profile. 14, 16, 18, 20, 22, 24, 26, 28, 30, 32,34, 36 mm 40/50/60/80/100 mm X 100 cm
262	Venous sinus obliquus self expanding nitinol stent High flexible with good strength.power crown. Homogeneous force distribution.Anchor ring. For venous obstruction closeto the bifurcation of the inferior vena cava. Anti jump technique..Introducer 10F. gUIDEWIRE 0.035\\" 14, 16 80/100/150 MM
263	Variable/Adjustable Compression Wraps are designed to aide people living with lymphedema, chronic edema, non Elastic Adjustable and reusable compression therapy wrap mimics the 50% overlap pre shaped curved straps for Upper limb (all Sizes)
264	Variable/Adjustable Compression Wraps are designed to aide people living with lymphedema, chronic edema, non Elastic Adjustable and reusable compression therapy wrap mimics the 50% overlap pre shaped curved straps for both hand & leg(All sizes)
265	A Latex Free Two-Component-System consists of an paddingcompression bandage which facilitates the wok flow and a cohesive compression bandage with patented Safe Lock Technology works on High working pressure & low resting pressure and is also washable & resuable. consisting of soft compression bandage (10 cm x 3.5 m) as first layer ;cohesive compression bandage (10 cm x 6 m) assecond layer.
266	Compression System for treatment of lymphological indications of upper and lower extremities consisting of 2 soft compression bandage , Elastic conforming bandages 4 cm x 4 m,Soft comression bandages 10 cm x 2.5 m x 0.2 cm,Foam Rubber pad bandage 10 cm x 1 m x 1 cm,short Strech bandage 6 cm x 5 m,short Strech bandage 8 cm x 5 m,short Strech bandage 10 cm x 5 m, short Strech bandage12 cm x 5 m
267	100% cotton wrap having lengthwise elasticity about 90%,high air permeability,textured fabric,cream colored,can be washed up to 50 times at 90 degree celcius 6 cmx5 mtr
268	100% cotton wrap having lengthwise elasticity about 90%,high air permeability,textured fabric,cream colored,can be washed up to 50 times at 90 degree celcius 10cmx5 mtr
269	100% cotton wrap having lengthwise elasticity about 90%,high air permeability,textured fabric,cream colored,can be washed up to 50 times at 90 degree celcius 8 cmx5 mtr
270	Bileaflet Prosthetic Heart Valve with curved leaflets - It Should be Curved Pyrolytic Carbon Leaflets. Aerofoil Housing Profile. Innovative Hinge Mechanism. Titanium Housing coated with Carbofilm. Soft Carbofilm coated swing ring. Should have an opening angle of 80 Degree. Should be FDA/CE approved. Should be in use universally for at least 15 years. Should be available in aortic and mitral all sizes.
271	BIEAFLET AORTIC VALVE WITH CONDUIT - Should have dacron/polyester. Should be collagen/gelatin impregnated to control hemostasis and reduce the hemorrhagic complications. Should have mechanical and bioprosthetic heart valve with low pressure gradients and leaflet opening 75 degree and more. Should have minimum taper conduit to facilitate strong coronary anastomosis. Should not have any pleats to allow easier positioning and attachment of the coronary arteries.Wide range of sizes 19mm to 33mm. Should have both CE and FDA approval. Dacron/Polyester graft 24mm to 34mm.
272	Tricuspid Ring 3D Rigid – Annuloplasty ring for tricuspid repair. Should be rigid three dimensional annuloplasty ring incomplete in shape to avoid interference to conduction system. Height should be less than 3.5mm. Additional septal lateral compression. Should have titanium core encapsulated with silicon and covered with polyester.Size – 26mm – 34mm. Should be US FDA/CE approved.
273	Mitral ring semi rigid – Composite annuloplasty ring for mitral. Semi rigid remodeling ring with anterior flexibility, posterior semi rigid. Should have polyester knit covering silicon core. Eyelet design to avoid ring dehiscense alloy encapsulated with silicon core and has polyester knit covering.Size – 26mm – 34mm. Should be US FDA/CE approved.
274	Pericardium Heart Valve with Carbofilm coated sewing cuff (MITRAL)The valve should be Bovine pericardium made of double sheet structure of Pericardium. The Leaflet of valve should be fixed on a flexible polymeric stent can tolerate under back pressure of 2.000mmHg The sweing cuff should be coated with Carbofilm to improve hemo-compatibilty.The tissue should be fixed with Glutraldehyde and then neutralized with Homocystic acid. It should be stored in a paraben solution and should not require rinsing of the valve.Size 25 to 31mm
275	Bovine Pericardium Heart Valve with Crown Design (AorticThe Leaflet of valve should be fixed on a flexible polymeric stent can tolerate under back pressure of 2.000mmHg2. Low Profile Height3. Sweing Cuff Diameter should be less4. The tissue anti calcification treatment should be fixed with Octanediol solution5. The tissue Used in the valve should be 100% Bovine Pericardium only. Size 19-29mm
276	Radiofrequency induced thermotherapy based catheter for the treatment of all grades of different kinds of varicose veins from the very small spider veins and perforating veins to Great Saphenous Vein (GSV), Catheters and the needles are connected to the central unit which generates the high frequency signal. Tissue is heated between 80ºC and 120ºC using catheter. Catheter should visual and audible indication for pull-back. All types of catheters should be use in single generator/machine for treatment of different kinds varicose veins,
277	Bovine pericardial patch - 8 cm x 8 cm, should be glutaraldehyde free. Should be storedin buffer solution.
278	Bovine pericardial patch - 6 cm x 6 cm, should be glutaraldehyde free. Should be storedin buffer solution.
279	Bovine pericardial patch - 4 cm x 4 cm, should be glutaraldehyde free. Should be storedin buffer solution.
280	All in one Closed IV catheter system with pre-attached high pressure extension set (up to 300PSI); with two split septum, closed system needle-less connectors; catheter made up of vailone with indwelling time of up to 144 hrs.; needle tip encapsulated in plastic cap for NSI prevention; ‘insta-flash’ technology for instant flash back. 20,22G
281	Dual port Closed needless connector with split spetum and transparent housing
282	Prefilled Terminally sterile single use device for flushing of catheters with heparinized saline,minimizing break loose contamination, pre labelled and pre color coded, avoiding medication error, 10 ml diameter barrel size, reducing increased flush pressure, Heparin is high molecular weight heparin, unfractionated, compliance to USP standard. 5ml 100IU
283	Prefilled Terminally sterile single use device for flushing of catheters with 0.9% saline solution having standard 10 ml syringe diameter with design to minimize syringe induces reflux. Should be latex & PVC free.The saline should be preservative free. 10 ml
284	Prefilled Terminally sterile single use device for flushing of catheters with 0.9% saline solution having standard 10 ml syringe diameter with design to minimize syringe induces reflux. Should be latex & PVC free.The saline should be preservative free. 5 ml
285	Prefilled Terminally sterile single use device for flushing of catheters with heparinized saline,minimizing break loose contamination, pre labelled and pre color coded, avoiding medication error, 10 ml diameter barrel size, reducing increased flush pressure, Heparin is high molecular weight heparin, unfractionated, compliance to USP standard. 5ml 10 IU
286	Sternum and ribs lock plateShould be available in different sizes and shapes to be supplied with Applier (gun). Sample based selection. should be US FDA approved
287	Sternum and ribs lock screw2.4mm and 2.7mm diameter cancellous self drilling locking screws with applier. Should be available in different sizes Sample based selection. should be US FDA approved
288	ePTFE CV patch - They are soft and pliable for easy surgical positioning and multidirectional oriented node fiber structure they have exceptional strength. Available in 0.4mm and 0.6mm thickness & 3cm x 6cm and 5cm x 7.5cm width, usage in cardiac and peripheral repairs. No preclotting and excellent biocompatibility
289	Eptfe PERICARDIAL Membrane – 6.0 CM X 12.0 CMS X 0.1MM
290	Eptfe PERICARDIAL Membrane – 12.0 CM X 12.0 CMS X 0.1MM
291	Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV2
292	Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV3
293	Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV4
294	Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV5
295	Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV6
296	Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV7
297	PTA Dilatation Catheter is a semi-compliant balloon catheter consisting of an over the wire (OTW) catheter with an angioplasty balloon fixed at the distal tip. Two radiopaque markers delineate the working length of the balloon and aid in balloon placement. in tended to dilate stenoses in theperipheral arteries, to treat obstructive lesions of native or synthetic AV fistulae and/ or re-expand endoluminal stent graft elements in the iliac arteries. 3-12 diameter rangeand 20-300 balloon length.
298	PTA Dilatation Catheters are recommended for use in percutaneous transluminal angioplasty (PTA) of the renal, popliteal, tibi al, femoral, and peroneal arteries. To facilitate catheter advancement through the vasculature and the vessel stenosis,Dual Layer Hydrophilic Coating is present on the distal segment of the shaft and the balloon
299	Should be use in Percutaneous Transluminal Angioplasty of the femoral, iliac, and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. High performance balloon catheter consisting of an overthe-wire catheter with a balloon fixed at the distal tip. The proprietary ultra non-compliant, low profile balloon is designed to provide consistent balloon diameters and lengths even at high pressures. Two radiopaque markers delineate the working length of the balloon and aid in balloon placement. The coaxial catheter includes a tapered atraumatic tip to facilitate advancement of the catheter to and through the stenosis
300	Should be for the treatment of atherosclerotic lesions in common and external iliac arteries with reference vessel diameters between 4.5 mm and 12.0 mm, and lesion lengths up to 100 mm. Balloon Expandable Vascular Covered Stent is comprised of an electropolished balloon-expandable stent made from 316L stainless steel, encapsulated between two layers of ePTFE. The covered stent is supplied pre- mounted on an over- the-wire delivery system with a non-compliant balloon
301	CO2 angiogaphy system. It should be preset to 1.3bar. It should enable a safe withdrawal of pure medical CO2 from gas bottles. It should be a two stage valve system. It should maintain a safe and constant pressure. It should feature a safety and release valve. Its connectors should be available in various International Standards. It should have a 1.5m length gas pipe line with connection to the CO2 pressure relief valve. It should have a special stop cock with 90degrees rotary valve for injection and loading procedure. It should have a dose chamber adjustable in 20ml steps with a locking slider for fixing the desired volume setting. It should have a 1.5m length connection tube to the patient
302	Distaflo cuff bypass graft are carbon imregnated inside and promotes natural hemodynamics, taper by 2mm over distal end. Flex small beading for torturous anatomy and 18mm arteriotomy for improved flow and increase wall shear stress with SmoothLaminar flow available in 60,70,80 cm lengths
303	Soft tissue retractor and protector with green and white rings
304	Perfadex solution for Lung Transplant
305	Cell saver Kit Compatable with existing machine
306	ECMO Disposable Kit compatible with existing machine
307	Eco Active:Photocatalytic dispersion anti bacterial Paint free from Biocides and PesticidesIt Should Produce anti bacterial, anti viral, anti fungal on the surfaces like, furniture, glass, door, walls floor, tilesColor should transluscent,or Semi transparentShould clean Air & Surfaces deodorise and should purifies the air and gives permanent effect for One year with detailed proofNo flammable, waterborne Invisible Ones applied Density 1.01 kg/lDoes not create a film, Yield : around 20m2/lt, Application temperature between 5 to 35 degree and /protect from frostTest Report from International acclaimed Certified Lab to be submitted. Product shouldbe Make In India. The product should be European CE Certified. The company should be EN 1499:2013
308	Alcohol based, quat based rapid surface wipes for gadgets and instruments for surface cleaning with minimum effectivity time on pathogens @ 30 seconds to 5 minutes only and ready to use. The wipe size should be min. 20cm x 25cm.Composition: -Each 100gm contains:1- propanol 30gm2- propanol 45gmDidecyle dimethyl ethyl ammonium chloride - 0.5gm n-Alkyl dimethylbenzyle ammonium chloride - 0.5gm poly hexa methylene Bigunide Hydrochloride- 0.5gm• ?with corrosion inhibitors and chelating agents &inert ingredientsTest report from NABL certified laboratory to be submitted. The product should be CE/IS certified. The product should be as per EN1500:2013 & ISO 9001
309	Antimicrobial Sponge – It should be a single use sterile sponge impregnated with 4% chlorhexidine Gluconate Antiseptic Solution for Surgical hand disinfection and skin antisepsis. It should have microbicidal activity against all gram negative and gram- positive bacteria, viruses and fungi.Composition: -Chlorhexidine Gluconate-20% v/v with organic surfactant and free from SLS with moisturiser and skin softener.• ?Test report from NABL certified laboratory to be submitted. The product should be CE/IS certified. The product should be as per EN1500:2013 & ISO 9001.
310	Quat Base Aldehyde free, bleach free, rapid surface disinfectant for medical Instruments & Electronic Devices.Composition: -Each 100gm contains:1- propanol 30gm2- propanol 45gmDidecyle dimethylethyl ammonium chloride - 0.5gm n-Alkyl dimethylbenzyle ammonium chloride - 0.5gm poly hexa methylene Bigunide Hydrochloride- 0.5gm• ?With corrosion inhibitors and chelating agents& inert Ingredients.• ?Should be effective against a wide variety of pathogenic microorganisms including bacteria antibiotic resistant bacteria, virus, fungus, mould etc.• ?Test report from NABL certified laboratory to be submitted. The product should be CE/IS certified. The product should be as per EN1500:2013 & ISO 9001.
311	Steriletransperantpolyurethaneadhesivecoatedsurgicalfilmwithsilverion Resistance to pH neutral water body fluid, detergent and alcohol Transparent and breathable surface and hold drape securely in place Efficiencyupto24hrTest Report from NABL Certified Lab to be submitted. The product should be CE/ISCertified . The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001
312	Sterile transperant polyurethane adhesive coated surgical film with povidone iodine Resistance to pH neutral water body fluid, detergent and alcoholTransparent and breathable surface and hold drape securely in place Efficiencyupto24hrTest Report from NABL Certified Lab to be submitted. The product should be CE/IS Certified . The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries
313	Sodium per Carbonate 43 gm. Tetraacetyleehtylenediamine 22gm. Oxygen Based Bleeching Agents>30% Non Ionic Surfactants <5% Phosphates <5%EDTA and salts thereof, enzymes perfumes <5%Test Report from NABL Certified Lab to be submitted. The product should be CE/IS Certified. The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries
314	Composition:Phosphoric acid 25% and cleaner.Instrument strains rust remover with chelating agent with amphoteric solution compatible with manual and ultrasonic machine.Test Report from NABL Certified Lab to be submitted. The product should be CE/ISCertified . The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001
315	Composition:ChlorohexidineGluconate 20% v/w with organic surfactants and free from SLS with moisture and skin softenerTest Report from NABL Certified Lab to be submitted. The product should be CE/IS Certified . The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries
316	NANOSOL GEL POLYMER60%C14, 30% C16,5% C12, 5% C18,…….10%68%C12,32% C14………10%INERT INGREDIENT ………80%USEPA registration number mandatory.USEPA certificate claim on N-Corona virus to be submitted.Test Report from Internationally acclaimed Certified Lab to be submitted. The product should be CE/ISO Certified. The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries. Certificate should be authorized by a Member of Multilateral recognition arrangement. American / European Certificate of Free sale mandatory. Product should be registered under FIFRA Section 3(c.)9 under the Provisions of PR Notice 98-10.
317	Enzymatic detergent consists of neutral ph. or low Alkaline to which one or more enzyme have been added tosurfactant and stabilizing agent. Protease, LipaseAmylase Cellulose.Test Report from NABL Certified Lab to be submitted. The product should be CE/IS Certified. The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries.
318	NaBo3-nH2o 50% w/wAldehyde free,Biodegradable, safe and non-Hazardous. It can be used for sterilization in all medicaldevice and instrumentTest Report from NABL Certified Lab to be submitted. The product should be CE/IS Certified. The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries.
319	Chlorhexidine Gluconate 2% W/v Isopropyl Alcohol 70% v/vTest Report from NABL Certified Lab to be submitted. The product should be CE/IS Certified. The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries
320	Composition: ChlorohexidineGluconate 20% v/w with organic surfactants and free from SLS with moisture and skin softener Test Report from NABL Certified Lab to be submitted. The product should be CE/IS Certified The company should be EN 1499:2013 Certified fo Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries and EN 12791:2016, ISO 9001:2015 and ISO 13485:2016 certicates should be attached. 500 ML
321	Paraffin Ip grade, non ionic surfactant contains butane, base should be highly purified mineral oil, for optimum lubrication Test Report from NABL Certified Lab to be submitted. The product should be CE/IS Certified. The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries. Pack size - 400ml and EN 12791:2016, ISO 9001:2015 and ISO 13485:2016 certicates should be attached. 400 ML
322	Pentazyme SolutionMulti-Enzyme Synergistic Blend (Pentazyme Complex): Incorporates five targeted enzymes—mannanase (for mannans), cellulase (for cellulose), xylanase (for hemicellulose), pectinase (for pectins), and beta-glucosidase (for final sugar release)—optimized in a proprietary ratio for 30-50% faster breakdown of lignocellulosic plant materials compared to single-enzyme products. This enables efficient decomposition in diverse applications, such as accelerating home composting or enhancing biofuel feedstock processing.pH-Adaptive Activation Technology: Engineered to activate optimally across a broad pH range (4.0-9.0) without needing buffers, allowing seamless integration into acidic soils, neutral cleaning solutions, or alkaline industrial processes. This reduces user preparation time and ensures consistent efficacy in variable environments, with stability up to 50°C for hot composting scenarios. Pack Size 1 Ltr. EN 12791:2016, ISO 9001:2015 and ISO 13485:2016 certificates should be attached. 1 Ltr
323	Advanced Fenton Booster Technology O3Di-hydrogen dioxide 24% and CH3CO3H 4.5 w/v, complies with CDC guidelines 2019, S. aureus ATCC 6538, E. hirae ATCC 10541, P. aeruginosa ATCC 15442, Candida Albicans, Mycobacterium Tuberculosis and Bacillus subtilis ATCC 6633, contact time less than 10 mins reports should be attached. Pack size 750 ML. EN 12791:2016, ISO 9001:2015 and ISO 13485:2016 certificates should be attached. 750 ml
324	Amino acid 5% 250ml without sorbitol and xylitol
325	L- arginine 10 gm sachet ( L- arginine 3.5 gm)
326	Integra is cannula without injection port with 10cm extension line .
327	Polyvinylidene Fluoride Monofilament 3/8 circle taper cutting , KL double armed , 6/0,10mm,60cm, dark blue monofilament Weavenit knitted of poly( ethylene terephtalate) , Pledget 23.50.4. Should be USFDA approved.
328	Polyvinylidene Fluoride Monofilament 3/8 circle taper cutting , KL double armed , 6/0,10mm,75cm, dark blue monofilament Weavenit knitted of poly( ethylene terephtalate) , Pledget 23.50.4. Should be USFDA approved.
329	Polyvinylidene Fluoride Monofilament 3/8 circle taper cutting , KL double armed , 5/0,13mm,75cm, dark blue monofilament Weavenit knitted of poly( ethylene terephtalate) , Pledget 23.50.4. Should be USFDA approved.
330	Polyvinylidene Fluoride Monofilament 3/8 circle taper cutting , KL double armed , 5/0, 13mm,75cm, dark blue monofilament Weavenit knitted of poly( ethylene terephtalate ),Pledget 350.4. Should be USFDA approved.
331	Polyamide 6.6 treated monofilament 3/8 circle Taper point/ round body, 4/0 DA, 16mm,80 cm < RB
332	Polyamide 6.6 treated monofilament 3/8 circle Taper point/ round body, 4/10 DA,20mm, 80 cm < RB < RB
333	Polyamide 6.6 treated monofilament 3/8 circle Taper point/ round body, 5/0 DA, 16mm,80 cm < RB
334	Polyamide 6.6 treated monofilament 3/8 circle Taper point/ round body, 6/0 DA, 10mm,80 cm < RB
335	Drape with size 55cm x 45 cm (Ahesive Area). Should be Gamma Sterilize. Should be polyurethane adhesive coated surgical film with povidone iodine. Transparent and breathable surface and hold drape securely in place. Test report from NABL certified lab to be submitted. The product should be CE/IS certified lab. The company should be EN 1499:2013. It Should be ISO 13485:2016 & ISO 9001:2015 approved. Certificate of Registrations issued by United Registrar of Systems. Document recognized by Member of Multilateral Recognition Arrangement. Certified by UKAS Management Systems
336	RFA catheter for the treatment of all grades of different kinds of varicose veins from the very small spider veins and perforating veins, Fistulas, haemorrhoids and fistulas.Catheters and the needles are connected to the central unit which generates the high frequency signal. Tissue is heated between 80ºC and 120ºC using catheter. Catheter should visual and audible indication for pull-back. All types of catheters should be use in single generator/machine for treatment of different kinds varicose veins, spider vein, hemorrhoids and fistulas
337	Dual Sheath 9Fr and 11Fr, ideal for Denali retrieval. Kink Resistant Nitinol Construction with Radiopaque Loop for Enhanced Visibility, 90° loop snare for proper loop placement with Precise 1:1 torque facilitates easy filter hook capture, Marker Bands for Accurate Positioning Convenient all-in-one kit includes new coaxial sheaths and hemostatic valve
338	Adhesive for treatment of varicose vein. It should be five (5) cc of the adhesive (a specially formulated n-butyl-2-cyanoacrylate) is contained within a screwed-capped vial. It should have dispenser gun consists of a pistol type, ergonomic handle with an integrated barrel and trigger. Each depression of the trigger delivers a controlled 0.10 cc (range: 0.06–0.12 cc) amount of adhesive. It should be 5 Fr with an effective length of 91 cm, laser markings at 3 cm and 85 cm from the tip, and high echogenic visibility. It should have introducer 7 Fr with an effective length of 80 cm and 10 mm spaced, circumferential markings along its length for measuring retraction length during the procedure. It should have dilator is 5 Fr with an effective length of 87 cm. It should have 3-cc syringes are graduated Monoject Luer Lock Syringes, each with a standard threaded luer lock connector. It should have dispenser tips are each comprised of a stainless steel, 1.5 mm ID, 3.8 cm length hypotube with a luer lock connector. It should have guidewire is a 0.035-inch, 180-cm J-wire guidewire
339	A non-adhesive liquid embolic agent comprised of EV0H (ethylene vinyl alcohol) copolymer dissolved in DMS0 (dimethyl sulfoxide), and suspended micronized tantalum powder. Liquid Embolic System should be available in one product formulation, 34L (8% EVOH). It should be with Liquid Embolic System EVOH & DMSO Compatible syringes to inject DMS0 and EVOH 34 L (8% EVOH)
340	It should have a uniqueness of both strength and flexibility combined. Item should have sterile packing. It should be a self-expanding and made of nitinol. It should have unique hybrid design which combines outstanding radial force with high flexibility which is necessary to overcome venous obstructions. It should have seamless and high grade electro polished. It should have anti-jump technique for exact stent placement The application device should be with radiopaque markers. It should have power crown. It should have a high flexibility and homogeneous force distribution. It should have Anchor ring. It should have braided sheath and atraumatic tip. It should be designed for treating venous obstructions close to the bifurcation of the inferior vena cava. It‘s design should offer the possibility to place the stent directly at the bifurcation. It should have Introducer Compatibility – 10F. It should have Guidewire Compatibility – 0.035 Inch. It should be available in various sizes :- 14/16/18 x 80/100/150mm
341	Item should have sterile packing. It should be a self-expanding and made of nitinol. It should have unique hybrid design which combines outstanding radial force with high flexibility which is necessary to overcome venous obstructions. It should have seamless and high grade electro polished. It should not have stent shortening during placement. The application device should be with radiopaque markers. It should have anti-jump technique for exact stent placement. It should have braided sheath and flexible tip. It should have independent ring system. It should have high vessel wall covering and homogeneous force distribution. It should have flash-links. It should have open cell design. It should have Introducer Compatibility – 10F. It should have Guidewire Compatibility – 0.035 Inch. It should be available in various sizes :- 12/14/16/18 x 60/80/100/120/150mm
342	It should be a self-expanding Nitinol stent. It should be indicated for use in IVC, SVC and Aorta. It should have a closed cell design. It should have high radial strength. It should not have significant stent shortening or lengthening. It should have Tantalum markers on stent for end visibility. It should have Anti-jump technique for exact stent placement. It should come with 6F application device for a smallest puncture site and also in 10F. The Application device should be with radiopaque markers. It should have braided sheath and flexible tip. It should have Atraumatic soft tip. Introducer Compatibility – 6F / 10F. Guidewire compatibility – 0.035 Inch. It should be available in various sizes:6F-14/16X30,40,60,80,100mm & 10F-18/20/22/24/2628/30/32 X 40/60/80,100mm
343	Varixio capsules for sclerotherapy by combining automation, safety, standardization, and superior foam quality, making it an ideal solution for effective and minimally invasive treatment of varicose veins. Sterile, single-use capsules that allow preparation of up to 10 ml of sclerosant foam for the treatment of varicose veins, haemorrhoids, and venousmalformations
344	Cryo ablation catheter for patients with lung cancer treatment. It should prosense cryoablation system provides a minimally-invasive solution for treating tumors with minimal discomfort and scarring. It should utilize the Liquid Nitrogen (LN2) based prosense Cryoablation System to be a promising treatment for tumors <1.8cm in size. Furthermore, LN2 systems have higher power and lower cost when compared to argongas cryoablation systems
345	Self-expanding frame, Supra-annular valve design, Bovine Pericardial Valve Proprietary Anti-calcification tissue treatmentExtended internal sealing skirtTwo rows of Radio-opaque markers on valve frame for implantation guidance Varying radial force frame – optimal forces at 3 parts of the frameLarge cell design in midframe for Coronary arteries access - Cell size of ≥ 15 French in mid-frameHighly flexible design and easy navigation CE & DCGI CertificationDelivery Catheter should have color-coded indicators for deployment guidance Ability to recapture, reposition and retrieve from upto 80% deployment level Atleast 5 Published studies and 250 patients data
346	ACCESSORIES KIT for TAVI
347	Temporary biosynthetic wound dressing - Denatured porcine dermal collagen is bonded to the nylon/ silicone membrane to provide a flexible and conformable dressing with adherence properties and a hydrophilic surface. Ultrathin, semi permeable, perforated silicone membrane that is mechanically bonded to a flexible knitted tri filament nylonfabric.13X13 CM
348	Temporary biosynthetic wound dressing - Denatured porcine dermal collagen is bonded to the nylon/ silicone membrane to provide a flexible and conformable dressing with adherence properties and a hydrophilic surface. Ultrathin, semi permeable, perforated silicone membrane that is mechanically bonded to a flexible knitted tri filament nylonfabric.13X38CM
349	Temporary biosynthetic wound dressing - Denatured porcine dermal collagen is bonded to the nylon/ silicone membrane to provide a flexible and conformable dressing with adherence properties and a hydrophilic surface. Ultrathin, semi permeable, perforated silicone membrane that is mechanically bonded to a flexible knitted tri filament nylonfabric.25X38 CM
350	Temporary biosynthetic wound dressing - Denatured porcine dermal collagen is bonded to the nylon/ silicone membrane to provide a flexible and conformable dressing with adherence properties and a hydrophilic surface. Ultrathin, semi permeable, perforated silicone membrane that is mechanically bonded to a flexible knitted tri filament nylonfabric. 38X50 CM
351	Transparent Film Roll – 10cm x 10mtr
352	Temporary biosynthetic wound dressing - Denatured porcine dermal collagen is bonded to the nylon/ silicone membrane to provide a flexible and conformable dressing with adherence properties and a hydrophilic surface. Ultrathin, semi permeable, perforated silicone membrane that is mechanically bonded to a flexible knitted tri filament nylon fabric. Gloves- Paediatric
353	Temporary biosynthetic wound dressing - Denatured porcine dermal collagen is bonded to the nylon/ silicone membrane to provide a flexible and conformable dressing with adherence properties and a hydrophilic surface. Ultrathin, semi permeable, perforated silicone membrane that is mechanically bonded to a flexible knitted tri filament nylon fabric. Gloves- Small
354	Temporary biosynthetic wound dressing - Denatured porcine dermal collagen is bonded to the nylon/ silicone membrane to provide a flexible and conformable dressing with adherence properties and a hydrophilic surface. Ultrathin, semi permeable, perforated silicone membrane that is mechanically bonded to a flexible knitted tri filament nylon fabric. Gloves- Medium
355	Temporary biosynthetic wound dressing - Denatured porcine dermal collagen is bonded to the nylon/ silicone membrane to provide a flexible and conformable dressing with adherence properties and a hydrophilic surface. Ultrathin, semi permeable, perforated silicone membrane that is mechanically bonded to a flexible knitted tri filament nylon fabric. Gloves- Large
356	VAC DRESSING - small polyurethane foam with ruler, drape and soft port.USFDA/CEcertified compatible with Renasys edge system
357	VAC DRESSING - medium polyurethane foam with ruler, drape and soft port.USFDA/CEcertified compatible with Renasys edge system
358	VAC DRESSING - Large polyurethane foam with ruler, drape and soft port.USFDA/CEcertified compatible with Renasys edge system
359	Canister 300 mL compatible with Renasys edge system
360	Canister 800 mL compatible with Renasys edge system
361	Topical skin adhesive
362	Poly(lactide-co-glycolide) Powered Absorabale Fixation device with counter display onfiring handle
363	Titanium Powered Non Absorabable Fixation device with counter display on firing handle
364	EU CE marked,EN13795,TUV approved with certified test for, Resistance to MicrobialPenetration test , 3-layered, 225 x 320, Fenestration, oval, lengthwise, off-centre, self- adhesive 11 x 22
365	EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test Back Table Cover-150 X 190,4 Towels-30 X 40,Instrument Placement- Mayo Stand 80 x 145,Adhesive Strip-9x50, swaddle cloth, fluid-absorbent nonwoven material 90 x 90,Opaque Layer, for the supine position, 230/200 x 312, with abdominalfenestration, 27 x 33
366	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
367	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 integratedtube fixations
368	Suture Stablilizer Transparent Carrier film skin-friendly polyacrylate adhesive with free of colophony and colophony derivatives with absorbent layer made of viscose/polyester, polyester/poly-ethylene wound contact 4x8 Inch,CE & ISO Certified
369	Suture Stablilizer Transparent Carrier film skin-friendly polyacrylate adhesive with free of colophony and colophony derivatives with absorbent layer made of viscose/polyester, polyester/poly-ethylene wound contact 4x10 Inch,CE & ISO Certified
370	wide retention polyester wound dressing having polyacrylate strip patterned adhesivecoating with MVTR more than 5000 g/m2/24hr and air permeability more than 4000 g/m2/24hr SIZE 10cmx2m,CE & ISO Certified
371	wide retention polyester wound dressing having polyacrylate strip patterned adhesive coating with MVTR more than 5000 g/m2/24hr and air permeability more than 4000g/m2/24hr. SIZE 10cmx10m,CE & ISO Certified
372	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
373	Bioactive dressing composed of a polyester lattice embedded in a polymer matrix, combined with Vaseline and hydrocolloid. Having size of 10x10 CM ,provide a moist environment conducive to healing while preventing adherence to the wound bed. The Vaseline component ensures hydration of dry wound areas and edges, promoting optimal wound care and patient comfort.
374	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
375	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
376	Sterile wound irrigation solution containing 0.1% Polyhexanide (PHMB) and 0.1% 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
377	Sterile wound irrigation solution containing 0.1% Polyhexanide (PHMB) and 0.1% 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
378	Sterile wound irrigation solution containing 0.1% Polyhexanide (PHMB) and 0.1% 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
379	Dressing shall comprise 100% 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
380	Dressing shall comprise 100% 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
381	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% polyamide, 42% cotton, 6% polyester, 4% elastane. Size-10cmx6 mtr
382	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% polyamide, 42% cotton, 6% polyester, 4% elastane. Size-8cmx6 mtr
383	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
384	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
385	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
386	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
387	Bioactive dressing composed of a polyester lattice embedded in a polymer matrix, combined with Vaseline and hydrocolloid. Having size of 10x10 CM ,provide a moist environment conducive to healing while preventing adherence to the wound bed. The Vaseline component ensures hydration of dry wound areas and edges, promoting optimal wound care and patient comfort.
388	Drape Set , 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
389	Drape Sheet ,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. U Drape Size :200 X 260
390	Extremity Sheet mention below specs,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 O Drape Size :225 x 320
391	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
392	Central Venous Catheter 3Fr/4FR 1 lumen/ 2 LUMEN with raulerson syringe to reduceblood loss, Non kinking guide wire made up of 45% titanium &55% nickel, with CE,ISO &HTCert certified
393	PT-INR STRIP for exiting machine for lumira dx machine
394	CRP STRIP for existing machine for lumira dx machine
395	D-DIMER for existing machine for lumira dx machine
396	Nt probnp- for existing machine for lumira dx machine
397	Pressure bag for infusion 500 mL
398	Pressure bag for infusion 1000 mL
399	Triicuspid Annuloplasty Ring:o rigid, 3D ring modeled on CT data from human tricuspid valves.o Should be in-plane 2D shape with 3D curvature, designed to follow the natural saddle shape of the valve.o Should be incomplete ring designed to avoid interference with the heart's conduction system.\\" remodeling device featuring a rigid component for stability and flexible segments to allow natural annulus motion during the cardiac cycle.o High-visibility white material, clearly marked sizes, and a semi- saddle design to match the natural annulus.
400	Soft , fibrous , bio absorbable hemostat.(ORC) 10.2*10.2 Please Enable Macros to View BoQ information

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Tender For Scardiothoracic Implants Ii , Silk 1 No 75Cm , Silk 1-0 R.C 75Cm , Silk 3-0 R.B. 75Cm , Silk 4-0 R.C. 75Cm , Silk 4-0 R.B. 75Cm , Umblical Tape 75Cm , Pacing Wire 2-0 18 Mm 75Cm , Pacing Wire 2-0 26 Mm 75Cm , Surgical Steel 4 No Cutting 48Mm ,, Jodhpur-Rajasthan

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Tender For Scardiothoracic Implants Ii , Silk 1 No 75Cm , Silk 1-0 R.C 75Cm , Silk 3-0 R.B. 75Cm , Silk 4-0 R.C. 75Cm , Silk 4-0 R.B. 75Cm , Umblical Tape 75Cm , Pacing Wire 2-0 18 Mm 75Cm , Pacing Wire 2-0 26 Mm 75Cm , Surgical Steel 4 No Cutting 48Mm ,, Jodhpur-Rajasthan

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