20(2025-26) 01 Tender for Cardiothoracic Implants (II) for CTVS Department

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

Surgical steel 4 no Blunt point R.B. 45MM

Surgical steel 5 no cutting 48 mm

Surgical steel 5 no Blunt point R.B. 45 mm

Surgical steel 6 no cutting 48 mm

Surgical steel 6 no Blunt point 45 mm

Polyester 2-0 10x75cm 17.5 mm

Polyester 2-0 10x75cm 17.5 mm 3x3x1.0 pledget

Polyester 2-0 10x75cm 26mm

Polyester 2-0 10x75cm 26mm 6x3x1.0 Pledget

Polyester 2-0 10x75cm 26mm 3x3x1.5 Pledget

Polyester 2-0 10x75cm 26mm 3x3x1.0 Pledget

Polyproplyne 2-0 17.5 mm D.A. 90 CM

Polyproplyne 2-0 17.5 mm D.A. 150 CM

Polyproplyne 2-0 26 mm D.A. 90 CM

Polyproplyne 2-0 26 mm D.A. 150 CM

Polyproplyne 3-0 17.5 mm D.A. 90 CM

Polyproplyne 3-0 25 mm D.A. 90 CM

Polyproplyne 3-0 26 MM D.A. 90 cm

Polyproplyne 4-0 13 MM D.A. 60 cm

Polyproplyne 4-0 16 MM D.A. 90 cm

Polyproplyne 4-0 17.5 mm D.A. 90 cm

Polyproplyne 4-0 17.5 mm D.A. 90 cm Pledget 3x3x1.5

Polyproplyne 4-0 20 mm D.A. 90 cm

Polyproplyne 4-0 26 mm D.A. 90 cm

Polyproplyne 4-0 26 mm D.A. 90 cm Pledget 3x3x.50

Polyproplyne 5-0 10 mm D.A. 60 cm

Polyproplyne 5-0 10 mm D.A. 75 cm

Polyproplyne 5-0 10 mm D.A. 60 cm Pledget 3x3x1.5

Polyproplyne 5-0 10 mm D.A. 75 cm Pledget 3x3x1.5

Polyproplyne 5-0 10 mm D.A. 75 cm Pledget 3x3x0.5

Polyproplyne 5-0 13 MM D.A. 60 cm pledget 3x3x1.5

Polyproplyne 5-0 13 MM D.A. 60 cm pledget 3x3x0.5

Polyproplyne 5-0 13 MM D.A. 75 cm pledget 3x3x0.5

Polyproplyne 5-0 13 MM D.A. 45 cm

Polyproplyne 5-0 13 MM D.A. 75 cm

Polyproplyne 5-0 16 MM D.A. 90 cm

Polyproplyne 5-0 16 MM D.A. 90 cm Pledget 3x3x1.5

Polyproplyne 5-0 20 MM D.A. 90 cm

Polyproplyne 6-0 10 MM D.A. 60 cm

Polyproplyne 6-0 10 MM D.A. 75 cm

Polyproplyne 6-0 10 MM D.A. 60 cm 3X3X1.5

Polyproplyne 6-0 10 MM D.A. 60 cm 3X3X0.5

Polyproplyne 6-0 13 MM D.A. 60 cm

Polyproplyne 6-0 13 MM D.A. 60 cm Black Needle

Polyproplyne 6-0 13 MM D.A. 45 cm

Polyproplyne 6-0 13 MM D.A. 75 cm

Polyproplyne 6-0 13 MM D.A. 90 cm

Polyproplyne 6-0 11 MM D.A. 60 cm

Polyproplyne 6-0 9 MM D.A. 60 cm

Polyproplyne 6-0 9 MM D.A. 75cm

Polyproplyne 7-0 9MM D.A. 60cm

Polyproplyne 7-0 9MM D.A. 75cm

Polyproplyne 7-0 9MM D.A. 60cm Black

Polyproplyne 7-0 9MM D.A. 60cm P V Needle

Polyproplyne 7-0 9MM D.A. 60cm C C Needle

Polyproplyne 7-0 10MM D.A. 60cm

Polyproplyne 7-0 8MM D.A. 60cm cc needdle

Polyproplyne 7-0 8MM D.A. 60cm P V Needle

Polyproplyne 7-0 8MM D.A. 60cm Black

Polyproplyne 8-0 6 MM D.A.60 cm

Polyproplyne 8-0 6.5 MM D.A.60 cm

Polyproplyne 8-0 9 MM D.A.60 cm

Polyproplyne 8-0 10 MM D.A.60 cm

Polyglactin 1 no R.B. 40 mm A.M. 90 cm

Polyglactin 1 no R.B. 40 mm A.M. 70 cm

Polyglactin 1 no R.B. 36 mm A.M. 120 cm

Polyglactin 1 no R.B. 36 mm A.M. 90 cm

Polyglactin 1 no.R.C. 40MM A.M. 90 cm

Polyglactin 1 no.Taper cut 40MM A.M. 90 cm

Polyglactin 1-0 no. R.B. 40MM A.M. 90 cm

Polyglactin 1-0 no.Taper cut 36MM A.M. 90 cm

Polyglactin 1-0 no.R.C. 36MM A.M. 90 cm

Polyglactin 1-0 no R.B. 30 mm A.M. 90 cm

Polyglactin 1-0 no R.B. 36 mm A.M. 90 cm

Polyglactin 2-0 R.B. 30 mm A.M. 90 CM

Polyglactin 2-0 R.B. 30 mm A.M. 70 CM

Polyglactin 2-0 R.B. 40 mm A.M. 90 CM

Polyglactin 2-0 R.C. 40 mm A.M. 90 CM

Polyglactin 2-0 R.B. 36 mm A.M. 90 CM

Polyglactin 3-0 R.C. 24 mm A.M. 70 CM

Polyglactin 3-0 R.B. 20 mm A.M. 90 CM

Polyglactin 4-0 R.B. 20 mm A.M. 70 CM

Polyglactin 5-0 R.B. 16 mm A.M. 45 CM

PGLA910 VIO 70CM 3-0 X 20MM 1/2 CIR TP

PGLA910 + VIO 90CM 2-0 X 30MM 1/2 CIR TP

POLYAMIDE BLK 70CM 2-0 X 45MM 3/8 CIR RC

POLY.P BLUE 90 CM 3-0 X 26MM 1/2 CIR TP DA CV

POLYAMIDE BLK 70CM 3-0 X 26MM 3/8 CIR RC

PGLA910 VIO 90CM 1X 40MM 1/2 CIR TIP HV

PDS VIO 150CM 1 X 50MM 1/2 CIR TP LP HV

PDS VIO 70CM 4-0 X 20MM 1/2 CIR TP LTP

PDS VIO 75CM 3-0 X 20MM 1/2 CIR TP DA

PDS VIO 90CM 1 X 40MM 1/2 CIR TP HV

POLY.P BLUE 70CM 2-0 X 30MM 1/2 CIR TP

POLY.P BLUE 70CM 0 X 30MM 1/2 CIR TP

POLY.P BLUE 70CM 0 X 30MM 1/2 CIR TP

POLY.P BLUE 70CM 1 X 40MM 1/2 CIR TP HV

POLY.P BLUE 90CM 2-0 X 30MM 1/2 CIR TP

POLY.P BLUE 90CM 4-0 X 25MM 1/2 CIR TC DA CV

POLY.P BLUE 90CM 0 X 30MM 1/2 CIR TP

POLY.P BLUE 90CM 0 X 30MM 1/2 CIR TP

POLY.P BLUE 70CM 4-0 X 16MM 1/2 CIR TP CV

POLY.P BLUE 70CM 3-0 X 25MM 1/2 CIR TP

POLY.P BLUE 70CM 1 X 30MM 1/2 CIR TP HV

POLY.P BLUE 70CM 1 X 30MM 1/2 CIR TP HV

POLY.P BLUE 75 CM 6-0 X 9MM 3/8 CIR TP DA CV

GUT CRMC 50CM 1 pre knot loop

PGLA910 VIO 90CM 1 X 40MM 1/2 CIR RC HV

PGLA910 VIO 90CM 2-0 X 40MM 1/2 CIR RC

PGLA910 VIO 35CM 1 X 23MM 1/2 CIR RC HV

PDS 1 no Loop

Absorbable Tacker

Absorbable tacker 30

Absorbable Tacker 20

Barb Sutures Polydiaxone 1-0 RB

Barb Sutures Poluglecaprone /Polyglactin 2-0

Barb sutures Polydiaxone 2-0

Barb(Polydiaxonone Violet) 30 cm 1-0 1/2 C.R.B.

Barb(Polydiaxonone Violet) 15 cm 1-0 1/2 C.R.B.

Barb(Polydiaxonone Violet) 30cm 1-0 1/2 C.R.B.

Barb(Polydiaxonone Violet) 45cm 1-0 1/2 C.R.B.

Barb(Polydiaxonone Violet) 45cm 2-0 1/2 C.R.B.

Barb(Polydiaxonone Violet) 45cm 2-0 1/2 C.R.B.

Barb(Polydiaxonone Violet) 25 cm 2-0 1/2 C.R.B.

Barb(Polydiaxonone Violet) 45cm 3-0 3/8 C. R.C.

Barb(Polydiaxonone Violet) 15 cm 3-0 1/2 C.R.B.

Barb(PGA-PCL UND) 36 cm 2-0

Barb(Polydiaxonone Violet) 30 cm 1-0

Barb(PGA-PCL UND) 30 cm 3-0

Barb(PGA-PCL UND) 30 cm 4-0

2 ml Fibrin sealant with synthetic Aprotinin 2ml Glu Dual tip syringe system and vials with sterile water for reconstitution should be part of the package.

4ml Fibrin sealant with synthetic Aprotinin 4ml Glu Dual tip syringe system and vials with sterile water for reconstitution should be part of the package.

10ml Fibrin sealant with synthetic Aprotinin 10 ml· Dual tip syringe system and vials with sterile water for reconstitution should be part of the package.

5 ml Hemostatic matrix with thrombin 5 ml . Pre-filled syringe of Bovine-derived Spherical Gelatin granule matrix along with a vial of human-derived Thrombin component (500IU/ml) & 0.9% Sodium Chloride

10 ml Hemostatic matrix with thrombin 10 ml. Pre-filled syringe of Bovine-derived Spherical Gelatin granule matrix along with a vial of human-derived Thrombin component (500IU/ml) & 0.9% Sodium Chloride

Resorbable Collagen based Sealing Hemostat- Material of Construction: Bovine Collagen patch, NHS-PEG 27mm * 27 mm

Resorbable Collagen based Sealing Hemostat- Material of Construction: Bovine Collagen patch, NHS-PEG 45mm * 45 mm

Resorbable Collagen based Sealing Hemostat- Material of Construction: Bovine Collagen patch, NHS-PEG : 45mm * 90 mm

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

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

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

Sensors for Bio Reactance non invasive monitor

Small size garments for vest airway machine

Medium size garments for vest airway machine

Large size garmets for Vest airway machine

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 .

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 .

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 .

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 .

PLP Chemoport with titanium internal chamber with silicone catheter 8 Fr-8.5 Fr

A sterile translucent adhesion barrier membrane composed of sodium hyaluronate and carboxymethyl cellulose full sheet 13x15 cm

A sterile translucent adhesion barrier membrane composed of sodium hyaluronate and carboxymethyl cellulose full sheet 13x7.5 cm

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

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

Cainester 500 ML. compatible to existing machine.

Human UC Dressing Allograft Strile Dehydrated human umblical cord derived membrane Allograft 5 cm x 3 cm

Human amniotic Allograft strile Dehydrated human amnion chorion menbrane with polyhexamethylene biguanide 11 cm x 7 cm

Human amnion chorion with PHMB Powder strile dehydrated human amnion chorion and polyhexamethylene biguanide powder 3 gm 10 ML

Human amniotic allograft strile dehydrated human amnion chorion membrane with polyhexamethylene biguanide 7 cm x 7 cm

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 n 10x10

Sterile Collagen sheets in Dry form. Pure Type 1&3 triple helical Membrane Bovine Origin Gamma sterilized and supplied in double sterile pouches. Biocompatible as per ISO 9001/ ISO13485 n 10x10

Sterile Collagen sheets in Dry form. Pure Type 1&3 triple helical Membrane Bovine Origin Gamma sterilized and supplied in double sterile pouches. Biocompatible as per ISO 9001/ ISO13485 n 10x20

Silicone sheet Pure Poly Siloxane based silicone scar management product in sheet form. 10x10

Biofil AB Sterils medicated collegan Particles 5 ML

Biofil AB Sterils medicated collegan Particles 10 ML

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

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

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

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 outer film with soft silicone adhesive border

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 outer film with soft silicone adhesive border

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 outer film with soft silicone adhesive border

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, lipophilic substances and silver salts)

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, lipophilic substances and silver salts)

Transperint dressing with absorbant Pad fully transprent backing, hypoallergenic acrylic adhesive 5x7 cm.

Transperint dressing with absorbant Pad fully transprent backing, hypoallergenic acrylic adhesive 6x10 cm.

Transperint dressing with absorbant Pad fully transprent backing, hypoallergenic acrylic adhesive 9x25 cm.

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 x 6cm.

Ventilator circuit 2 water trap with MDI Adoptor Plain. MD/5 Approved

Ventilator circuit with MDI Adoptor Single water trap. MD/5 Approved

Bain circuit Adult with tubing. MD/5 Approved

Bain circuit Pediatric with tubing. MD/5 Approved

DLT all Sizes

Pur-Xro 28G/1fr PICC catheter 1261.203 20cm length with stylet, spliting introducer needle,securing wings, measuring tape and every cm marking , flow rate 0.7ml/min with 8 cm extension tubing and clamp

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.

Pur-xro 22G catheter 1212 with stight guidwire and introducer with integral extension and clamp . Length 4,6,8,10,20cm

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

XRO ICD Trocar drain with catheter for Pleural drainage of newborn Size 8Fr and 10 Fr.

Ultrasound guided Nerve stimulation needle with transparent hub and 50cm detachable extension.

Dialyzer with Tubing 1.4 Single use With Steam sterlization. Filter and Tubing Should be same manufacterur

Dry Bicarbonate Bag 650 Gm Bibag. Compatible with fresenius Machine.

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 oflimescale and have disinfection and decalcification in one process.

Diasafe

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

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

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

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

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

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

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

ACT Crtidge Compatable with existing machine (medtronic)

Snare Adult

Snare

Catheter MPA

catheter MA

Catheter Pigtail

Angioseal

Diagnostic Tiger cath

Diagnostic Tiger cath

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.

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.

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.

Valvoplasty balloon catheters size 10-22 mm nominal pressure < 4 ATM

Balloon in Balloon BIB Catheters USFDA

Z Med type Balloon for Aortic Coarctation

CP stent uncovered Without Balloon Mounted 8zig

CP stent uncovered Without Balloon Mounted 10zig

CP stent uncovered With Balloon Mounted 8zig

CP stent uncovered With Balloon Mounted 10zig

CP stent covered Without Balloon Mounted 8zig

CP stent covered Without Balloon Mounted 10zig

CP stent covered With Balloon Mounted 8zig

CP stent covered With Balloon Mounted 10zig

Long sheath

Devil sheath

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. Patented butterfly upstream pivot design

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.Reduce leaflet stress.

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.

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

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

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 to 34mm.

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

Vessel harvesting system

The Endoscopic Harvesting System should be designed for use in conjunction with the 7mm Endoscope. Harvesting Cannula should have four lumens to house the Endoscope, C-Ring, Distal Lens Washer Tube &amp; BiSECTOR Bipolar Ligating Forceps for ligation &amp; 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 to provide a port of access for insertion of endoscopic instruments into an incision site.syringe should be provided for inflation/deflation of the Balloon.

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,

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,

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

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

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

Oxynator 1.5 Ltr

Oxynator 4 Ltr

Hemofilter Adult

Hemofilter Ped.

CABG KIT ON PUMP annexure 1

Double Valve Surgery Kit annexure 2

Toff Surgery Kit annexure 3

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

LB Bifurgateed bifurcate grafts has unique hydrolysable gelatin inpregnation , proven twillweave base fabric , superb handling , Excellent suture retention , Cardiothoracic and abdominal aplications . Gelweave

LB St. grafts has unique hydrolysable gelatin inpregnation , proven twillweave base fabric , superb handling , Excellent suture retention , Cardiothoracic and abdominal aplications . Gelweave St

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 (4 Branches)

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.

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

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

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

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)

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)

A Latex Free Two-Component-System consists of an padding compression 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) as second layer.

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

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

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

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

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.

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.

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.

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.

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

Bovine Pericardium Heart Valve with Crown Design (Aortic The Leaflet of valve should be fixed on a flexible polymeric stent can tolerate under back pressure of 2.000mmHg 2. Low Profile Height 3. Sweing Cuff Diameter should be less 4. The tissue anti calcification treatment should be fixed with Octanediol solution 5. The tissue Used in the valve should be 100% Bovine Pericardium only. Size 19-29mm

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,

Bovine pericardial patch - 8 cm x 8 cm, should be glutaraldehyde free. Should be stored in buffer solution.

Bovine pericardial patch - 6 cm x 6 cm, should be glutaraldehyde free. Should be stored in buffer solution.

Bovine pericardial patch - 4 cm x 4 cm, should be glutaraldehyde free. Should be stored in buffer solution.

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

Dual port Closed needless connector with split spetum and transparent housing

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 100 IU

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

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

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

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

Eptfe PERICARDIAL Membrane – 6.0 CM X 12.0 CMS X 0.1MM

Eptfe PERICARDIAL Membrane – 12.0 CM X 12.0 CMS X 0.1MM

Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV2

Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV3

Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV4

Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV5

Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV6

Cardio Vascular Suture made of Polyltetraflurothylene Double ended sizes CV7

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 the peripheral 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 range and 20-300 balloon length.

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

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

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

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

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 Smooth Laminar flow available in 60,70,80 cm lengths

Soft tissue retractor and protector with green and white rings

Perfadex solution for Lung Transplant

Cell saver Kit Compatable with existing machine

ECMO Disposable Kit compatible with existing machine

Eco Active:Photocatalytic dispersion anti bacterial Paint free from Biocides and Pesticides It Should Produce anti bacterial, anti viral, anti fungal on the surfaces like, furniture, glass, door, walls floor, tiles Color should transluscent,or Semi transparent Should clean Air & Surfaces deodorise and should purifies the air and gives permanent effect for One year with detailed proof No flammable, waterborne Invisible Ones applied Density 1.01 kg/l Does not create a film, Yield : around 20m2/lt, Application temperature between 5 to 35 degree and /protect from frost Test Report from International acclaimed Certified Lab to be submitted. Product should be Make In India. The product should be European CE Certified. The company should be EN 1499:2013

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 30gm 2- propanol 45gm Didecyle 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 ingredients 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

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.

Quat Base Aldehyde free, bleach free, rapid surface disinfectant for medical Instruments & Electronic Devices. Composition: - Each 100gm contains: 1- propanol 30gm 2- propanol 45gm Didecyle 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.

Steriletransperantpolyurethaneadhesivecoatedsurgicalfilmwithsilverion Resistance to pH neutral water body fluid, detergent and alcohol Transparent and breathable surface and hold drape securely in place Efficiencyupto24hr 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

Sterile transperant polyurethane adhesive coated surgical film with povidone iodine Resistance to pH neutral water body fluid, detergent and alcohol Transparent and breathable surface and hold drape securely in place Efficiencyupto24hr 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

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

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/IS Certified . The company should be EN 1499:2013 Certified for Chemical Disinfectant and antiseptics & ISO 9001

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 for Chemical Disinfectant and antiseptics & ISO 9001:2015 by a notified body in regulated countries

NANOSOL GEL POLYMER 60%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.

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.

NaBo3-nH2o 50% w/w Aldehyde free,Biodegradable, safe and non-Hazardous. It can be used for sterilization in all medicaldevice and instrument 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.

Chlorhexidine Gluconate 2% W/v Isopropyl Alcohol 70% v/v 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

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

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

Pentazyme Solution Multi-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

Advanced Fenton Booster Technology O3 Di-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

Amino acid 5% 250ml without sorbitol and xylitol

L- arginine 10 gm sachet ( L- arginine 3.5 gm)

Integra is cannula without injection port with 10cm extension line .

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 2*3.5*0.4. Should be USFDA approved.

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 2*3.5*0.4. Should be USFDA approved.

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 2*3.5*0.4. Should be USFDA approved.

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 3*5*0.4. Should be USFDA approved.

Polyamide 6.6 treated monofilament 3/8 circle Taper point/ round body, 4/0 DA, 16mm, 80 cm < RB

Polyamide 6.6 treated monofilament 3/8 circle Taper point/ round body, 4/10 DA, 20mm, 80 cm < RB < RB

Polyamide 6.6 treated monofilament 3/8 circle Taper point/ round body, 5/0 DA, 16mm, 80 cm < RB

Polyamide 6.6 treated monofilament 3/8 circle Taper point/ round body, 6/0 DA, 10mm, 80 cm < RB

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

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

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

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

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)

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

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

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

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 venous malformations

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 argon gas cryoablation systems

Self-expanding frame, Supra-annular valve design, Bovine Pericardial Valve Proprietary Anti-calcification tissue treatment Extended internal sealing skirt Two rows of Radio-opaque markers on valve frame for implantation guidance Varying radial force frame – optimal forces at 3 parts of the frame Large cell design in midframe for Coronary arteries access - Cell size of ≥ 15 French in mid-frame Highly flexible design and easy navigation CE & DCGI Certification Delivery 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

ACCESSORIES KIT for TAVI

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.13X13 CM

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.13X38CM

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.25X38 CM

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. 38X50 CM

Transparent Film Roll – 10cm x 10mtr

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

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

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

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

VAC DRESSING - small polyurethane foam with ruler, drape and soft port.USFDA/CE certified compatible with Renasys edge system

VAC DRESSING - medium polyurethane foam with ruler, drape and soft port.USFDA/CE certified compatible with Renasys edge system

VAC DRESSING - Large polyurethane foam with ruler, drape and soft port.USFDA/CE certified compatible with Renasys edge system

Canister 300 mL compatible with Renasys edge system

Canister 800 mL compatible with Renasys edge system

Topical skin adhesive

Poly(lactide-co-glycolide) Powered Absorabale Fixation device with counter display on firing handle

Titanium Powered Non Absorabable Fixation device with counter display on firing handle

EU CE marked,EN13795,TUV approved with certified test for, Resistance to Microbial Penetration test , 3-layered, 225 x 320, Fenestration, oval, lengthwise, off-centre, self- adhesive 11 x 22

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 abdominal fenestration, 27 x 33

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

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

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

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

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

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

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

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.

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

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

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

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

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

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

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

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

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

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

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

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

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

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.

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

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

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

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

Central Venous Catheter 3Fr/4FR 1 lumen/ 2 LUMEN with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45% titanium &55% nickel, with CE,ISO &HTCert certified

PT-INR STRIP for exiting machine for lumira dx machine

CRP STRIP for existing machine for lumira dx machine

D-DIMER for existing machine for lumira dx machine

Nt probnp- for existing machine for lumira dx machine

Pressure bag for infusion 500 mL

Pressure bag for infusion 1000 mL

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.

Soft , fibrous , bio absorbable hemostat.(ORC) 10.2*10.2

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