Tender For RATE CONTRACT FOR SPECIAL CONSUMABLE ITEMS FOR PATIENTS USE IN GMERS GENERAL HOSPITAL, HIMMATNAGAR in India

Work Detail

RATE CONTRACT FOR SPECIAL CONSUMABLE ITEMS FOR PATIENTS USE IN GMERS GENERAL HOSPITAL, HIMMATNAGAR- radiosterlized 10 cm pur single lumen closed iv access device, multipurpose, needle free, reduces risk of air embolism and blood loss, neutral mechanism for blood reflux (eu-ce & us-fda approved only), radiosterlized 10 cm pur double lumen closed iv access device, multipurpose, needle free, reduces risk of air embolism and blood loss, neutral mechanism for blood reflux(eu-ce & us-fda approved only), radiosterlized 10 cm pur triple lumen closed iv access device, multipurpose, needle free, reduces risk of air embolism and blood loss, neutral mechanism for blood reflux (eu-ce & us-fda approved only), endotracheal with side port for surfactant supply to new born size 2.0/2.5/3.0/3.5 (eu-ce & us-fda approved only), lisa catheter is a peba transparentcatheter of 20 cm long, with an outer diameter of 6fr and a centimeter marking to guide insertion. (eu-ce & us-fda approved only), peripherally inserted central venous polyurethane catheter with stylet long term: size :- 28 g, 20 cm, fr – 1 (premicath)(eu-ce & us-fda approved only), peripherally inserted central venous polyurethane catheter for long term : size :- 24 g, 30 cm, fr – 2 (nutriline)(eu-ce & us-fda approved only), pur umbilical catheter radiopaque and transparent with pe 2 way stop cock with two colour code. size fr- 2.5, length-30 cm numerical marking from 4 to 25cm (eu-ce & us-fda approved only), pur umbilical catheter radiopaque and transparent with pe 2 way stop cock with two colour code. size fr- 3.5, length-30 cm numerical marking from 4 to 25cm (eu-ce & us-fda approved only), pur umbilical catheter radiopaque and transparent with pe 2 way stop cock with two colour code. size fr- 4.0 / 5.0 length-30 cm numerical marking from 4 to 25cm (eu-ce & us-fda approved only), pur umbilical catheter double lumen radiopaque and transparent with pe 2 way stop cock with two colour code. size fr- 4.0 / 5.0 length-40 cm numerical marking from 4 to 25cm (eu-ce & us-fda approved only), antimicrobial ag expert umbilical catheter radiopaque and transparent with pe 2 way stop cock with two colour code. size fr- 2.5/3.5/4.0/5.0, length-30 to 40 cm numerical marking from 4 to 25cm (eu-ce & us-fda approved only), antimicrobial ag expert double umbilical catheter radiopaque and transparent with pe 2 way stop cock with two colour code. size fr- 4.0 / 5.0 length-40 cm numerical marking from 4 to 25cm (eu-ce & us-fda approved only), inter costal drainge xro thoracic trocar fr. 8.0 / 10 / 12 for pleural drainage in neonates with heimlich valve for trocar adaptor to connect icd bag with trocar(eu-ce & us-fda approved only) (eu-ce & us-fda approved only), neohelp™ is a polyethylene occlusive sterile suit used immediately after birth to prevent heat loss of the newborn. adjustable hood, double layer of polyethylene, pre-shaped foam cushion, central opening (eu-ce & us-fda approved only), endotoxin 0.22 micron, triple layer 96 hour iv filter with 10 cm extension flow rate - 6ml/min(eu-ce & us-fda approved only), single lumen catheter for multi purposes - leaderflex catheter 22g – 4/6/8/10/15/20 cm with 17ml/min flow rate, introducer needle 21g, 42 mm length, straight guidewire 0.46 mm, 230 mm length(eu-ce & us-fda approved only), single lumen catheter for multi purposes - leaderflex catheter 20g – 4/6/8/12 cm with 30ml/min flow rate, introducer needle 20g, 38 mm length, straight guidewire 0.50 mm, 200 mm length(eu-ce & us-fda approved only), single lumen catheter for multi purposes - leaderflex catheter 18g – 6/10 cm with 55ml/min flow rate, introducer needle 19g, 54 mm length, straight guidewire 0.7 mm, 200 mm length(eu-ce & us-fda approved only), double lumen polyurethan flexane catheter cvc line, 3 fr x 6 cm / 10 cm/ 15 cm (eu-ce & us-fda approved only), double lumen polyurethan flexane catheter - 4.5fr length 6cm/12.5cm/20cm/30cm (lumen 20g, 20g) 1 introducer needle,1 short iv cannula 22g- l-25mm, j tipped nickel titanium antikink guidewire with teflon coating, 2 dilators (length-38mm)(eu-ce & us-fda approved only), triple lumen polyurethan flexane catheter - 4.5fr l-6 cm/8cm/10cm/12.5cm/20cm/30cm (lumen 20g/23g/23g) 1 introducer needle,1 short iv cannula 22g- l-25mm, j tipped nickel titanium antikink guidewire with teflon coating, 2 dilators (length-38mm)(eu-ce & us-fda approved only), triple lumen polyurethan flexane catheter - 5.5fr l-8cm/12.5cm/15cm/20cm/30 cm (lumen 19g/21g/21g) 1 introducer needle,1 short iv cannula 22g- l-25mm, j tipped nickel titanium antikink guidewire with teflon coating, 2 dilators (length-38mm)(eu-ce & us-fda approved only), double lumen polyurethan flexane catheter - 5.5fr l-8 cm/12.5cm/15cm/30cm (lumen 17g/17g) 1 introducer needle,1 short iv cannula 22g- l-25mm, j tipped nickel titanium antikink guidewire with teflon coating, 2 dilators (length-38mm)(eu-ce & us-fda approved only), smart midline is ct rated midline (up to 325psi and 1.5ml/s*) – a class ii device. it is simple and quick to place using the direct seldinger technique. suitable for a wide range of clinical indications from 2fr x 4cm/6cm/8 cm/10cm/15cm/20cm, it is also an integrated extension line, which helps to reduce the risk of post insertion complications. puncture needle 21g - 4.5 cm echogenic (eu-ce & us-fda approved only), smart midline is ct rated midline (up to 325psi and 1.5ml/s*) – a class ii device. it is simple and quick to place using the direct seldinger technique. suitable for a wide range of clinical indications from 3fr x 6cm/8 cm/10cm/12cm/15cm/20cm, it is also an integrated extension line, which helps to reduce the risk of post insertion complications. puncture needle 21g - 4.5 cm echogenic (eu-ce & us-fda approved only), smart midline is ct rated midline (up to 325psi and 5ml/s*) – a class ii device. it is simple and quick to place using the direct seldinger technique. suitable for a wide range of clinical indications from 4fr x 8 cm/10cm/12cm/15cm/20cm/25cm, it is also an integrated extension line, which helps to reduce the risk of post insertion complications. puncture needle 21g - 4.5 cm echogenic (eu-ce & us-fda approved only), lectrocath pe extension line for infusion pump with grip colour code. 10/50/100/150/200 cm (eu-ce & us-fda approved only), lectrocath pe extension spiral line for infusion pump with grip colour code. 100/150/200 cm(eu-ce & us-fda approved only), quincke needle for lumbar puncture- 22g l-120/150 mm (eu-ce & us-fda approved only), whitacre pencil point needle for lumbar puncture- 25g l-120mm (eu-ce & us-fda approved only), pead. spinal needle with quincke bevel g-25 l-50 / 38 mm with introducer, l- 50mm (eu-ce & us-fda approved only), daul guidance nerve block needle 20g-22g 20 degree bevel 25mm / 35mm / 50mm / 85mm / 100mm / 120mm / 150mm (eu-ce & us-fda approved only), continuous nerve block catheter for long surgery 5/10/15 cm (eu-ce & us-fda approved only), multicath 7.5 fr x 12.5 cm with distal lumen 14g, safety needle for prevention of needlestick injuries and blood exposure, safety scalpel for sharp injuries avoidance, bls valve to prevent blood spillage and exposure reduction, nitinol & teflon coated j tip guidewire 58.8cm, 0.88mm (eu-ce & us-fda approved only), multicath expert (antimicrobial) 7.5 fr x 16 cm with distal lumen 14g, safety needle for prevention of needlestick injuries and blood exposure, safety scalpel for sharp injuries avoidance, bls valve to prevent blood spillage and exposure reduction, nitinol & teflon coated j tip guidewire 58.8cm, 0.88mm (eu-ce & us-fda approved only), multistar (antimicrobial) 7.5 fr x 16 cm with distal lumen 14g, safety needle for prevention of needlestick injuries and blood exposure, safety scalpel for sharp injuries avoidance, bls valve to prevent blood spillage and exposure reduction, nitinol & teflon coated j tip guidewire 58.8cm, 0.88mm (eu-ce & us-fda approved only), epidural set of 18g needle and 20 g polyurethan epidural catheter with filter and 10 ml lor syringe (eu-ce & us-fda approved only), polyurethan epidural catheter size : 20 g (eu-ce & us-fda approved only), cse set, tuohy needle with backeye-18g l-80mm,pencil point spinal needle-27g/25g l-118mm,10ml syringe with lor technique, peribax epidural catheter 20g with closed tip,three lateral eye and flat filter 0.22 micron. (it should be us-fda and eu-ce approved), pead epidural set with 19g needle and 24g catheter with lor syringe (eu-ce & us-fda approved only), nerve stimulator with side control keys and safety button (eu-ce & us-fda approved only), paediatric 1.2 micron charged polysulphon 24 hr lipid filter, air eliminating filter- flow rate-136ml/min (it should be us-fda and eu-ce approved), triple lumen polyurethane catheter for haemodialysis and high volume infusions.fully radiopaque catheter introduced by the seldinger technique. flexible fixation wings and polyurethane extension tubes with cl . centimetre graduations from 9 cm from the distal tip. the (green) hub of the distal lumen allows administration of drugsduring haemodialysis. flexible distal tip.the clip allows the pigtails to be held in a curved position.tray presentation containing:- 1 triple lumen catheter (xro - pur) 12fr- 1 introducer needle ø 1.1 x 1.4 mm - length 70 mm- 1 graduated j guidewire and guidewire advancer – length 70 cm- 2 injection caps- 2 dilators- 1 scalpel. (it should be us-fda and eu-ce approved), antimicrobial double-lumen polyurethane catheter for haemodialysis.fully radiopaque catheter introduced by the seldinger technique. flexible fixation wings and polyurethane extension tubes with cl . centimetre graduations from 9 cm from distal tip.the active ingredient used in the expert technology is the silver ion-based antimicrobial agentwhich is incorporated into the polyurethane tubing of the catheter.tray presentation containing:- 1 double-lumen catheter (pur – xro) 12fr- 1 introducer needle ø 1.1 x 1.4 mm - length 70 mm- 1 graduated j guidewire and guidewire advancer - length 60 cm- 2 injection caps- 2 dilators- 1 scalpel. (it should be us-fda and eu-ce approved), antimicrobial double-lumen polyurethane catheter for haemodialysis.fully radiopaque catheter introduced by the seldinger technique. flexible fixation wings and polyurethane extension tubes with cl . centimetre graduations from 9 cm from distal tip.the active ingredient used in the expert technology is the silver ion-based antimicrobial agentwhich is incorporated into the polyurethane tubing of the catheter.tray presentation containing:- 1 double-lumen catheter (pur – xro) 10fr- 1 introducer needle ø 1.1 x 1.4 mm - length 70 mm- 1 graduated j guidewire and guidewire advancer - length 60 cm- 2 injection caps- 1 dilator- 1 scalpel. (it should be us-fda and eu-ce approved), antimicrobial triple lumen polyurethane catheter for haemodialysis.fully radiopaque catheter introduced by the seldinger technique. flexible fixation wings and polyurethane extension tubes with cl . centimetre graduations from 9 cm from distal tip. the (green) hub of the distal lumen allows administration of drugs during haemodialysis.the active ingredient used in the expert technology is the silver ion-based antimicrobial agent which is incorporated into the polyurethane tubing of the catheter.tray presentation containing:- 1 triple lumen catheter (pur – xro) 12fr- 1 introducer needle ø 1.1 x 1.4 mm - length 70 mm- 1 graduated j guidewire and guidewire advancer - length 60 cm- 2 injection caps- 2 dilators (8 fr and 12 fr)- 1 scalpel (it should be us-fda and eu-ce approved), radial, femoral arterial pe catheter with anti kinking color & fixation wings, straight guide wire, introducer needle. catherter size g-20/18, length 8,10 cm (it should be us-fda and eu-ce approved), radial artery catheter pe 20g 8cm. kit must bls valve and visualisation chember to avoid blood exposure to air and prevent from needle stick injury. device must support in confirmation of arterial puncture. (it should be us-fda and eu-ce approved), a usfda & ce-eu approved 3 layered antimicrobial barrier dressing with silcryst nanocrystals silver consisting of a rayon/polyester non- woven core laminated (by sonic welds) between an upper & lower layer of nanocrystalline silver coated high density polyethylene mesh which releases 70-100ppm of silver continuously for 72 hours. 10cm x 10 cm, a usfda & ce-eu approved 3 layered antimicrobial barrier dressing with silcryst nanocrystals silver consisting of a rayon/polyester non- woven core laminated (by sonic welds) between an upper & lower layer of nanocrystalline silver coated high density polyethylene mesh which releases 70-100ppm of silver continuously for 72 hours. 10cm x 120 cm, a usfda & ce-eu approved 3 layered antimicrobial barrier dressing with silcryst nanocrystals silver consisting of a rayon/polyester non- woven core laminated (by sonic welds) between an upper & lower layer of nanocrystalline silver coated high density polyethylene mesh which releases 70-100ppm of silver continuously for 72 hours. 20cm x 40 cm / 40cm x 40 cm, a usfda & ce-eu approved 5 layered antimicrobial barrier dressing with silcryst nanocrystals silver, consisting of a 2 layers of rayon/polyester non- woven core laminated (by sonic welds) between an 3 layers of nanocrystalline silver coated high density polyethylene mesh which releases 70-100ppm of silver continuously for 7 days. 5cm x 5 cm, a usfda & ce-eu approved 5 layered antimicrobial barrier dressing with silcryst nanocrystals silver, consisting of a 2 layers of rayon/polyester non- woven core laminated (by sonic welds) between an 3 layers of nanocrystalline silver coated high density polyethylene mesh which releases 70-100ppm of silver continuously for 7 days. 10cm x 12.5 cm, a usfda & ce-eu approved 5 layered antimicrobial barrier dressing with silcryst nanocrystals silver, consisting of a 2 layers of rayon/polyester non- woven core laminated (by sonic welds) between an 3 layers of nanocrystalline silver coated high density polyethylene mesh which releases 70-100ppm of silver continuously for 7 days. 15cm x 15 cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 12.5cm x 12.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 12.5cm x 17.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 22.5cm x 22.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. sacral shape patch 17cm x 17cm, a usfda & ce-eu approved triple layered antimicrobial non- adhesive hydrocellular foam dressing for superior fluid handling through unique dressing reconstruction with a breathable pink coloured polyurethane film, middle ayer highly absorbent silver sulfadiazine containing hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. suitable for use under compression 10 x 10cm, a usfda & ce-eu approved triple layered antimicrobial non- adhesive hydrocellular foam dressing for superior fluid handling through unique dressing reconstruction with a breathable pink coloured polyurethane film, middle ayer highly absorbent silver sulfadiazine containing hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. suitable for use under compression 20 x 20cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 10cm x 10cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 12.5cm x 12.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 17.5cm x 17.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 22.5cm x 22.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 7.5cm x 7.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. sacral shape dressing size 17cm x 17cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising strong acrylic adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. sacral shape dressing size 22cm x 22cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 7.5cm x 7.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 12.5cm x 12.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 17.5cm x 17.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, ssd containing middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. 22.5cm x 22.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. the dressing is cuttable that makes it suitable for awkward and high patient movement areas. 7.5cm x 7.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. the dressing is cuttable that makes it suitable for awkward and high patient movement areas. 10cm x 10cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. the dressing is cuttable that makes it suitable for awkward and high patient movement areas. 12.5cm x 12.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. the dressing is cuttable that makes it suitable for awkward and high patient movement areas. 17.5cm x 17.5cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. the dressing is cuttable that makes it suitable for awkward and high patient movement areas. a unique winged shape dressing that can be used on heels, elbow and back. size : 23cm x 23.2cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. the dressing is cuttable that makes it suitable for awkward and high patient movement areas. 10cm x 20cm / 10cm x 25cm / 10cm x 30cm / 15cm x 15cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. the dressing is cuttable that makes it suitable for awkward and high patient movement areas. suitable for application on sacral area. 16.8cm x 17.1cm, a usfda & ce-eu approved 3 layered hydrocellular foam with low allergy / nonsensitising gentle silicon adhesive and multiway stretch technology which helps keep the dressing securely in place without adhering to the wound. a breathable pink coloured polyurethane film, middle layer which is a highly absorbent hydrocellular foam and a perforated non-adherent wound contact layer which prevents healing tissue from growing into the dressing minimizing pain on removal. the dressing is cuttable that makes it suitable for awkward and high patient movement areas. suitable for application on sacral area. 21.6cm x 23cm, a usfda & ce-eu approved unique quadrilobe shape with a wide border, designed to fit the contours of the human body securely, flexible multi-layered (5 layered) design incorporating hydrocellular foam helps in managing friction and shear to prevent pressure injury. exulock advanced lock in - excellent fluid locking under pressure helps in leakage prevention. exumask change indicator: unique change indicator helps patients know the best time to change dressing. silicone wound contact layer offers minimal pain and discomfort on removal while allowing it to be repositioned. patented polyurethane breathable top film that is both showerproof and a bacterial barrier. size : 10.3cm x 10.3cm / size : 12.9cm x 12.9cm / size : 15.4cm x 15.4cm / size : 21cm x 21cm, a usfda & ce-eu approved unique quadrilobe shape with a wide border, designed to fit the contours of the human body securely, flexible multi-layered (5 layered) design incorporating hydrocellular foam helps in managing friction and shear to prevent pressure injury. exulock advanced lock in - excellent fluid locking under pressure helps in leakage prevention. exumask change indicator: unique change indicator helps patients know the best time to change dressing. silicone wound contact layer offers minimal pain and discomfort on removal while allowing it to be repositioned. patented polyurethane breathable top film that is both showerproof and a bacterial barrier. in a butterfly shape to be used in awkward areas like heel, elbow and back. size : 25cm x 25.2cm, a usfda & ce-eu approved unique quadrilobe shape with a wide border, designed to fit the contours of the human body securely, flexible multi-layered (5 layered) design incorporating hydrocellular foam helps in managing friction and shear to prevent pressure injury. exulock advanced lock in - excellent fluid locking under pressure helps in leakage prevention. exumask change indicator: unique change indicator helps patients know the best time to change dressing. silicone wound contact layer offers minimal pain and discomfort on removal while allowing it to be repositioned. patented polyurethane breathable top film that is both showerproof and a bacterial barrier. in a sacral shape size : 17.2cm x 17.5cm, a usfda & ce-eu approved unique quadrilobe shape with a wide border, designed to fit the contours of the human body securely, flexible multi-layered (5 layered) design incorporating hydrocellular foam helps in managing friction and shear to prevent pressure injury. exulock advanced lock in - excellent fluid locking under pressure helps in leakage prevention. exumask change indicator: unique change indicator helps patients know the best time to change dressing. silicone wound contact layer offers minimal pain and discomfort on removal while allowing it to be repositioned. patented polyurethane breathable top film that is both showerproof and a bacterial barrier. in a sacral shape size : 21.6cm x 23cm, ce eu certified sterile clear amorphous hydrogel containing 77.7 percent aqueous base 2.3 percent carboxy methyl cellulose and 20 percent propylene glycol bacteriostatic with non adherent applicator system for simple directable and controlled application even in awkward wound sites size 15 gram or 25 gram, a ce-eu certified patented technically advanced self adhesive medical grade silicone gel sheet made specifically for day and night use. it is a soft and occlusive silicon sheet that is designed to soften, flatten and fade red, dark or raised scars on any part of the body. it is comfomable & can be easily washed & reused upto 28 days. size : 12cm x 15cm, a ce-eu certified patented technically advanced self adhesive medical grade silicone gel sheet made specifically for day and night use. it is a soft and occlusive silicon sheet that is designed to soften, flatten and fade red, dark or raised scars on any part of the body. it is comfomable & can be easily washed & reused upto 28 days. size : 12cm x 6cm, ce eu certified moisture responsive ported catheter dressing with high moisture vapour transmission rate 3000 to 1000 gram per square meter at 37 degree celsius for 24 hours made up of transparent bacteria proof reactive polyurethane film consisting of patented grid pattern with low allergy water based acrylic adhesive only on 75 percent of the dressing for easy application removal and reduction in lateral migration ported peripheral iv line dressing size 5 cm x 6 cm or 6 cm x 7 cm or 7 cm x 9 cm, ce eu certified moisture responsive ported catheter dressing with high moisture vapour transmission rate 3000 to 1000 gram per square meter at 37 degree celsius for 24 hours made up of transparent bacteria proof reactive polyurethane film consisting of patented grid pattern with low allergy water based acrylic adhesive only on 75 percent of the dressing for easy application removal and reduction in lateral migration non ported central line iv dressing size 10 cm x 12 cm or 10 cm x 14 cm or 9 cm x 12 cm, ce-eu certified low adherent absorbent wound dressing consists of an absorbent cotton and polyester fibre pad which is heat bonded to a thin low adherent perforated wound contact layer, with an outer hydrophobic non-woven layer which is highly conformable and can be cut to shape to apply on awkward area, shows delayed risk of exudate strike-through to the outer dressing surface, low risk of fibre shed or new tissue cell growth from the wound into the absorbent pad. size : 20cm x 10cm, ce-eu certified low adherent absorbent wound dressing consists of an absorbent cotton and polyester fibre pad which is heat bonded to a thin low adherent perforated wound contact layer, with an outer hydrophobic non-woven layer which is highly conformable and can be cut to shape to apply on awkward area, shows delayed risk of exudate strike-through to the outer dressing surface, low risk of fibre shed or new tissue cell growth from the wound into the absorbent pad. size : 50cm x 7mtr, a high moisture vapour permeable transparent, bacterial barrier film dressing to help minimise the risk of infection. it is comprised of a water proof patented low friction polyurethane film with acrylic adhesive that allows excess moisture to evaporate through the dressing while maintaining a moist wound healing environment for faster healing and less risk of skin maceration. it helps to minimise the risk of secondary infection as it aids the prevention of bacterial contamination of the wound by providing bacterial barrier. size : 6cm x 7cm / size : 10cm x 12cm, a ce-eu certified usfda approved non glaring, highly extensible surgical drape with low allergy adhesive. the breathability and permeability prevent moisture build up on skin surface during surgery, it also provides bacterial barrier and protects the surrounding skin during surgery by being conformable and elastic. size : 10cm x 14cm / 15cm x 28cm, a ce-eu certified usfda approved non glaring, highly extensible surgical drape with low allergy adhesive. the breathability and permeability prevent moisture build up on skin surface during surgery, it also provides bacterial barrier and protects the surrounding skin during surgery by being conformable and elastic. size : 30cm x 28cm / 45cm x 28cm, a ce-eu certified usfda approved non glaring, highly extensible surgical drape with low allergy adhesive. the breathability and permeability prevent moisture build up on skin surface during surgery, it also provides bacterial barrier and protects the surrounding skin during surgery by being conformable and elastic. size : 40cm x 42cm / 45cm x 55cm, a ce-eu certified usfda approved trasnparent, waterproof, low friction film which helps minimise the friction, also providing bacterial barrier to aid in preventition of external contamination of wound. this extensible film designed to conform to contours of the patients body allowing movement whilst dressing is in place. it allows patient to shower with the film in place and it also minimises exposure to ultra violet light. top prelift film has a graph grid to measure wound area. size : 5cm x 10mtr / size : 10cm x 10mtr, a ce-eu certified usfda approved low allergy adhsive with high mvtr patented reactic film and low adherent absorbent pad which reduces the risk of skin maceration by keeping the exudate away from the wound area, while also providing bacterial barrier to prevent bacterial contamination. the post operative dressing is conformable and have low pain upon removal. size : 6.5cm x 5cm / pad size : 4cm x 2.5cm, a ce-eu certified usfda approved low allergy adhsive with high mvtr patented reactic film and low adherent absorbent pad which reduces the risk of skin maceration by keeping the exudate away from the wound area, while also providing bacterial barrier to prevent bacterial contamination. the post operative dressing is conformable and have low pain upon removal. size : 9.5cm x 8.5cm / pad size : 7.3cm x 3.7cm, a ce-eu certified usfda approved low allergy adhsive with high mvtr patented reactic film and low adherent absorbent pad which reduces the risk of skin maceration by keeping the exudate away from the wound area, while also providing bacterial barrier to prevent bacterial contamination. the post operative dressing is conformable and have low pain upon removal. size : 15.5cm x 8.5cm / pad size : 12cm x 3.7cm, a ce-eu certified usfda approved low allergy adhsive with high mvtr patented reactic film and low adherent absorbent pad which reduces the risk of skin maceration by keeping the exudate away from the wound area, while also providing bacterial barrier to prevent bacterial contamination. the post operative dressing is conformable and have low pain upon removal. size : 20cm x 10cm / pad size : 15cm x 5.6cm, a ce-eu certified usfda approved low allergy adhsive with high mvtr patented reactic film and low adherent absorbent pad which reduces the risk of skin maceration by keeping the exudate away from the wound area, while also providing bacterial barrier to prevent bacterial contamination. the post operative dressing is conformable and have low pain upon removal. size : 25cm x 10cm / pad size : 20cm x 5.6cm, a ce-eu certified usfda approved low allergy adhsive with high mvtr patented reactic film and low adherent absorbent pad which reduces the risk of skin maceration by keeping the exudate away from the wound area, while also providing bacterial barrier to prevent bacterial contamination. the post operative dressing is conformable and have low pain upon removal. size : 30cm x 10cm / pad size : 25cm x 5.6cm, a ce-eu certified usfda approved low allergy adhsive with high mvtr patented reactic film and low adherent absorbent pad which reduces the risk of skin maceration by keeping the exudate away from the wound area, while also providing bacterial barrier to prevent bacterial contamination. the post operative dressing is conformable and have low pain upon removal. size : 35cm x 10cm / pad size : 30cm x 5.6cm, a biosynthetic semipermeable membrane designed to temporarily perform the functions of lost epidermis until reepithelialization. it is bilaminate material, consisting of a woven nonbiodegradable nylon mesh, the outer surface which has silastic coating to provide vapor loss and bacterial ingress. pptides derived from porcine type 1 collagen are bonded to all exposed nylon silicon surface. the membrane bonds firmly to the adequately prepared bed of a superificial partial thickness or middermal injury until spontaneous detachment by reeithelialization. size : 13cm x 13cm, a biosynthetic semipermeable membrane designed to temporarily perform the functions of lost epidermis until reepithelialization. it is bilaminate material, consisting of a woven nonbiodegradable nylon mesh, the outer surface which has silastic coating to provide vapor loss and bacterial ingress. pptides derived from porcine type 1 collagen are bonded to all exposed nylon silicon surface. the membrane bonds firmly to the adequately prepared bed of a superificial partial thickness or middermal injury until spontaneous detachment by reeithelialization. size : 13cm x 38cm, a biosynthetic semipermeable membrane designed to temporarily perform the functions of lost epidermis until reepithelialization. it is bilaminate material, consisting of a woven nonbiodegradable nylon mesh, the outer surface which has silastic coating to provide vapor loss and bacterial ingress. pptides derived from porcine type 1 collagen are bonded to all exposed nylon silicon surface. the membrane bonds firmly to the adequately prepared bed of a superificial partial thickness or middermal injury until spontaneous detachment by reeithelialization. size : 25cm x 38cm, a biosynthetic semipermeable membrane designed to temporarily perform the functions of lost epidermis until reepithelialization. it is bilaminate material, consisting of a woven nonbiodegradable nylon mesh, the outer surface which has silastic coating to provide vapor loss and bacterial ingress. pptides derived from porcine type 1 collagen are bonded to all exposed nylon silicon surface. the membrane bonds firmly to the adequately prepared bed of a superificial partial thickness or middermal injury until spontaneous detachment by reeithelialization. size : 50cm x 38cm, a biosynthetic semipermeable membrane designed to temporarily perform the functions of lost epidermis until reepithelialization. it is bilaminate material, consisting of a woven nonbiodegradable nylon mesh, the outer surface which has silastic coating to provide vapor loss and bacterial ingress. pptides derived from porcine type 1 collagen are bonded to all exposed nylon silicon surface. the membrane bonds firmly to the adequately prepared bed of a superificial partial thickness or middermal injury until spontaneous detachment by reeithelialization. size : glove pediatric / glove small / medium / large, it is a biosynthetic wound dressing constructed of a silicone film bonded to a cross linked collagen coated nylon fabric. a non toxic mixture of highly purified peptides derived from porcine dermal collagen has been bonded to the nylon/silicone membrane to provide a highly flexible and conformable composite dressing. the semi permeable silicone membrane controls water vapour loss at rates comparable to normal skin. it helps to minimize dead space on the wound surface and minimises the proliferation of bacteria. it is transparent and allows for visualisationof the wound site. size 13cm x 13cm / size 13cm x 38cm / size 25cm x 38cm / size 38cm x 50cm, it is a biosynthetic wound dressing constructed of a silicone film bonded to a cross linked collagen coated nylon fabric. a non toxic mixture of highly purified peptides derived from porcine dermal collagen has been bonded to the nylon/silicone membrane to provide a highly flexible and conformable composite dressing. the semi permeable silicone membrane controls water vapour loss at rates comparable to normal skin. it helps to minimize dead space on the wound surface and minimises the proliferation of bacteria. it is transparent and allows for visualisationof the wound site. size : pediatric size glove / small size glove / medium size glove / large size glove, a ce-eu certified single use disposable handpiece to be used with hydrosugery powered device for surgical wound debridement. producing high pressure jet of sterile saline, creating venturi chest at the distal tip of the hand piece, to precisely select, excise and evacuate nonviable tissue, bacteria and contaminants from wounds, burns and soft tissue injuries. the handpiece travels tangentially over the soft tissue surface it creates a smooth wound bed while maximising dermal preservation. the tissue-preserving technique reduces time to closure which may reduce overall treatment costs. size : 14mm x 45 / size : 14mm x 15 / size : 8mm x 45, ce-eu certified single time use portable negative pressure wound therapy system with a small portable sterile pump maintaining a consistent negative pressure of 80mmhg evenly at the wound surface through pioneering arilock technology and to be used for 7 days which manages exudate without cannister through a combination of absorption in waterproof & bacteria proof superabsorbent core locking exudate away from the wound and evaporation of moisture through the outer high mvtr film of the dressing. dressing size 10cm x 20cm / 10cm x 30cm / 10cm x 40cm / 15cm x 15cm / 15cm x 20cm / 15cm x 30cm / 20cm x 20cm / 25cm x 25cm, ce-eu certified single time use portable negative pressure wound therapy system with a small portable sterile pump maintaining a consistent negative pressure of 80mmhg evenly at the wound surface through pioneering arilock technology and to be used for 14 days which manages exudate without cannister through a combination of absorption in waterproof & bacteria proof superabsorbent core locking exudate away from the wound and evaporation of moisture through the outer high mvtr film of the dressing. dressing size 10cm x 20cm / 10cm x 30cm / 10cm x 40cm / 15cm x 15cm / 15cm x 20cm / 15cm x 30cm / 20cm x 20cm / 25cm x 25cm, 1) non-woven viscose rayon porous backing, coated with pressure sensitive, hypoallergic acrylate adhesive.2) it is a hypoallergenic tape and has negligible potential for skin irritation.3) it should have iso 10993 biocompatibility testing for medical devices as well as human repeat insult patch test (hript) and human cumulative irritation patch test (hcipt).4) who gmp certified and iso 13485 certificated facility.5) size - 1/2 * 9.1m / 1 * 9.1m / 2 * 9.1m / 3 * 9.1m, 1) non-woven viscose rayon porous backing, coated with pressure sensitive, hypoallergic acrylate adhesive with dispenser2) it is a hypoallergenic tape and has negligible potential for skin irritation.3) it should have iso 10993 biocompatibility testing for medical devices as well as human repeat insult patch test (hript) and human cumulative irritation patch test (hcipt).4) who gmp certified and iso 13485 certificated facility.5) size - 1 * 9.1m / 2 * 9.1m / 3 * 9.1m, perforated, porous thus breathable polyethylene, transparent backing with straight bi-directional tear, coated with pressure sensitive, hypoallergic acrylate adhesive. size - 1*9.1m / 2*9.1m / 3*9.1m, woven ,no- stretch silk- like cloth tape for critical tubing application (g.m.p., fda, isi, qci certified as applicable). tested as per iso 10993 for biocompatability as well as human repeat insult patch test (hript) and human cumulative irritation patch test (hcipt). (g.m.p., fda, isi, qci certified as applicable) size : 1 / 2 / 3 inch (box), rayon and polyester fiber with resin copolyester film, silicone release coating and bi-directional tear-ability. size - 1in * 5.5 yd / size - 2in * 5.5 yd, single, sterile, transparent, semi-permeable thin conformable polyurethane film (latex free), it is water, virus and bacteria proof, it is coated with water repellent hypo-allergic pressure sensitive acrylate adhesive, unique paper window frame delivery design. it has a slit to conform around the piv hub. microporous documentation strip. size - 6*7 cm. / size - 7*8.5 cm. who-gmp and iso 13485 certified., single, sterile, transparent, semi-permeable thin conformable polyurethane film (latex free), one half laminated with soft cloth breathable backing for enhanced grip on challenging, it is water, virus and bacteria proof, it is coated with water repellent hypo-allergic pressure sensitive acrylate adhesive,unique paper window frame delivery design, prolonged dressing wear time, it has a slit to conform around the cvc hub. microporous documentation strip. size - 8.5 * 11.5 cm. who-gmp and iso 13485 certified., single, sterile, transparent, semi-permeable thin conformable polyurethane film (latex free), it is water, virus and bacteria proof, it is coated with water repellent hypo-allergic pressure sensitive acrylate adhesive, unique paper window frame delivery design. it has a slit to conform around the cvc hub. microporous documentation strip. size - 10*12 cm / size: 6.5cm x 7cm / size: 8.5cm x 11.5cm, peripheral iv line kit consisting of 1 piece advanced reinforced iv dressing size 7 cm x 6.5 cm transparent semipermeable breathable water proof bacterial and viral barrier synthetic blood penetration resistance sterile polyurethane film peripheral iv dressing for adults reinforced with soft cloth border and notch non latex hypoallergenic pattern coated acrylic adhesive picture frame delivery system with 2 large extra sterile soft cloth tape strips for additional securement and complies with iso 10993 standards for biocompatibility 1 piece of 2 percent weight by volume chlorhexidine gluconate and 70 percent volume by volume isopropyl alcohol skin prep swab 1 piece latex free disposable tourniquet and 1 piece sterile gauze swab, transparent, semipermeable, breathable, water proof, bacterial and viral barrier, synthetic blood penetration resistance, sterile, polyurethane film peripheral iv dressing for adults reinforced with soft cloth border and notch. non-latex, hypoallergenic pattern coated acrylic adhesive. it has a picture frame delivery system with 2 large extra sterile soft cloth tape strips for additional secural and complies with iso-10993 standards for biocompatibility. size: 3.8cm x 4.5cm, transparent, semipermeable, breathable, water proof, bacterial and viral barrier, synthetic blood penetration resistance, sterile, polyurethane film central line iv dressing containing chlorhexidine gluconate gel pad provides antimicrobial activity for upto 10 days, reinforced with soft cloth border and notch. non-latex, hypoallergenic pattern coated acrylic adhesive. it has a picture frame delivery system and complies with iso-10993 standards for biocompatibility. size - 8.5 * 11 cm / size - 7 * 8.5 cm, sterile, semipermeable, transparent, breathable, water proof, bacterial and viral barrier polyurethane film (that reduces chance of infection) with absorbent, non-adherent pad (that helps reduce trauma on dressing removal) and latex free hypoallergenic acrylic adhesive that is gentle to skin. it has a picture frame delivery system to enable easy application. size - 5*7 cm / size - 6*10 cm, sterile, semipermeable, transparent, breathable, water proof, bacterial and viral barrier polyurethane film (that reduces chance of infection) with absorbent, non-adherent pad (that helps reduce trauma on dressing removal) and latex free hypoallergenic acrylic adhesive that is gentle to skin. it has a picture frame delivery system to enable easy application. size - 9*10 cm / 9*15 cm / 9*20 cm / 9*25 cm / 9*35 cm, sterile, semipermeable, transparent, breathable, water proof, bacterial and viral barrier polyurethane film (that reduces chance of infection) with absorbent, non-adherent pad (that helps reduce trauma on dressing removal) and latex free hypoallergenic acrylic adhesive that is gentle to skin. it has a picture frame delivery system to enable easy application., fine quality elastic crepe bandage with fast edges manufactured as per din standards. 10/15 cm, disposable surgical clipper blade with ribbed design to remove all types of surgical procedure, body hair , head hair , including sensitive area of the body with single blade (dry and wet).cuts away from the skin positioning with width of 36.4mm. surgical hair removal equipment should have a run time of around 160 minutes on a 4 hour recharge, disinfectant for pre surgery patient bathing should include chg 4 percent 100 ml solution with medical grade polyurethane open cell foam density of 28.8 to 35.2 kg per cubic meter disinfectant should have iso 10993 part 10 2010 en 1040 2005 en 1275 2005 usp 36 fungicidal and sporicidal and hcipt certifications it should also comply with astm 2315, surgical hand antiseptic solution with a composition of chlorhexidine gluconate 1 percent solution and ethyl alcohol 61 percent weight by weight must be waterless scrub that reduces the usage of water sterile towels scrub brushes and hand rub must contain emollient rich lotion base and moisturizer to help prevent dry cracked hands and should provide rapid antimicrobial kill must meet cdc who and aorn guidelines for hand hygiene size 500 ml, incisde drape made up of polyester film with an acrylic adhesive that contains a complex of iodoform(n- vinyl 2 pyrrolidine) with a iodine concentration of 0.092 mg iodine/cm2. film should be breathable and conformable to skin, compatible with povidone and chg skin preps. iodine from the drape should be present in the deepest skin layers (1000 microns depth) where hair folices exist apart from killing microbes on skin layer. size 26x20 cm with frame delivery mechanism which allow application by single person., incisde drape made up of polyester film with an acrylic adhesive that contains a complex of iodoform(n- vinyl 2 pyrrolidine) with a iodine concentration of 0.092 mg iodine/cm2. film should be breathable and conformable to skin, compatible with povidone and chg skin preps. iodine from the drape should be present in the deepest skin layers (1000 microns depth) where hair folices exist apart from killing microbes on skin layer. size 34x35 cm, incisde drape made up of polyester film with an acrylic adhesive that contains a complex of iodoform(n- vinyl 2 pyrrolidine) with a iodine concentration of 0.092 mg iodine/cm2. film should be breathable and conformable to skin, compatible with povidone and chg skin preps. iodine from the drape should be present in the deepest skin layers (1000 microns depth) where hair folices exist apart from killing microbes on skin layer. size 56x45 cm, iso 11140-1:2014 type 5 integrating indicators, moving front chemical integrators to verify all perimeters of steam sterilization together i.e. time, temperature and quality of steam. read out indicates accept or reject after processing. individually packaged and labeled with lot number and expiration date on each roll. vibrant color branding (red and green) at the flip side to quickly locate the ci in a pack/set. us fda 510k cleared third party/bsi kitemark testing to validate that iso 11140- 1:2014 type 5 requirements are met and certificates are available, iso 11140-1:2014 and 11140-5:2007 designed for testing air-removal efficiency of 132-134°c (270- 273°f) dynamic-air removal steam sterilizers test pack will reproducibly detect residual air in the sterilizer chamber due to air leaks, air removal failures and inadequate vacuum by testing the air removal efficiency of 132-134°c (270- 273°f) dynamic air-removal steam sterilizers indicator sheet will turn a uniform dark color except when air removal failures, such as air leaks, occur. lead free equivalent in performance to the bowie-dick towel pack described in ansi/aami st79 does not change visually 24 months when properly stored includes a scanable 2d bar code with lot number and expiration date for record keeping includes a process indicator on the test pack label preassembled, single use designed for consistent performance results ink pattern design for easy interpretation two year shelf life sheet can be filed for record keeping, • rapid readout biological indicators containing a standardized, viable population of bacillus atropheus spores for eto sterilization cycles• the indicator detects the presence of viable spores by the production of fluorescence within 4 hours in conjunction with rapid readout incubator• designed and certified as per iso 11138 and en 866.• should be compliant to iso 11138-1:2006(en) part 1 and iso 11138-1:2006(en) part 2• every box should contain quality assurance certificate with mention of spore population, d- value & z value, • rapid readout biological indicators for steam sterilization containing a standardized, viable population of bacillus stearothermophilus spores• the indicator detects the presence of viable spores by the production of fluorescence in 3 hours in conjunction with rapid readout incubator• designed and certified as per iso 11138 and en 866.• should be compatible with the following cycles:a) 121-123°c gravity steam sterilization cycleb) 132-135°c vacuum-assisted steam sterilization cycles.• should be compliant to iso 11138-1:2006(en) part 1 and iso 11138-1:2006(en) part 3• every box should contain quality assurance certificate with mention of spore population, d- value & z value• should have cfg from us fda, rapid readout biological indicators for steam sterilization containing a standardized, viable population of bacillus stearothermophilus spores• the indicator detects the presence of viable spores within 24 mins in conjunction with super rapid readout incubator• designed and certified as per iso 11138 and en 866.• should be compatible with the pre vacuum cycle of 132°c to 135°c• should be compliant to iso 11138-1:2006(en) part 1 and iso 11138-1:2006(en) part 3• every box should contain quality assurance certificate with mention of spore population, d- value & z value, • rapid readout biological indicators for vaporized hydrogen peroxide sterilization containing a standardized, viable population of bacillus stearothermophilus spores• the indicator detects the presence of viable spores within 24mins in conjunction with rapid readout incubator• designed and certified as per iso 11138 and en 866.• should be compatible with amsco® vpro® max low temperature sterilization system (lumen, non lumen, and flexible cycles), and in sterrad® 100s, sterrad® nx (standard and advanced cycles) and 100nx (standard, flex, express and duo cycles) systems.• should be compliant to iso 11138-1:2006(en) part 1 and iso11138-1:2006(en) part 2• every box should contain quality assurance certificate withmention of spore population, d- value & z value, multiple enzymatic concentrate solution with lipases, cellulases, proteases andamylases, should be usable for manual, ultra sonic and automatic cleaning systems.should have scale inhibition, rust inhibition & shine retention properties. film based polymer technology with controlled enzyme release. dilution rate should be 7ml/ltr for heavy instruments., an alcohol-free liquid barrier film containing acrylate terpolymer, polyphenylmethylsiloxane, hexamethyldisoloxane and isooctane which dries quickly to form a breathable, transparent, hypoallergenic, non-cytotoxic coating to protect damaged or intact skin from friction, moisture, shear, bodily fluids, incontinence and adhesive trauma. proven to protect from iad for 72 hours. size -28ml spray bottle, an alcohol-free liquid barrier film containing acrylate terpolymer, polyphenylmethylsiloxane, hexamethyldisoloxane and isooctane which dries quickly to form a breathable, transparent, hypoallergenic, non-cytotoxic coating to protect damaged or intact skin from friction, moisture, shear, bodily fluids, incontinence and adhesive trauma. proven to protect from iad for 72 hours. size -3ml wand, should be a multi variable chemical indicator for vh2o2 designed for critical variables such as time temperature and vh2o2 concentration should have color changing technology changing from blue to pink on exposure to all critical variables and should provide a clear accept or reject readout for instant result interpretation each chemical indicator should be clearly marked for use in vh2o2 sterilizer and identified as type 4 chemical indicator shelf life up to 2 years each chemical indicator must be labeled with lot number after sterilization the indicator should not visually change color within 6 months when stored under recommended conditions vibrant color branding should be provided for quick identification of the chemical indicator in a pack or set provision of barcode on each chemical indicator to upload information to hospital instrument tracking system, dispoable transparent nasogastric securement device with non- adhesive tab for easy removal. it should have fiber mesh backing for extra strength.manufacture must have europeance certified, fda approved & iso 13485:2016 certified., 10 percent povidone iodine usp equivalent to 1 percent available iodine gmp fda isi qci certified as applicable, purpose to be used as antiseptic solution for proper hand hygiene and infection control composition 4 percent chlorhexidine or propanol based container must have attached pump for dispensing accurate amount of solution should have facility to fit on wall or hang from bed gmp fda isi qci certified as applicable size 100 ml or 500 ml, purpose to be used as antiseptic solution for proper hand hygiene and infection control composition 4 percent chlorhexidine or propanol based container must have attached pump for dispensing accurate amount of solution should have facility to fit on walls or hang from bed gmp fda isi qci certified as applicable size 500 ml, non woven viscose rayon porous backing coated with pressure sensitive hypoallergenic acrylate adhesive hypoallergenic tape with negligible potential for skin irritation should have iso 10993 biocompatibility testing for medical devices as well as human repeat insult patch test hript and human cumulative irritation patch test hcipt manufactured in who gmp certified and iso 13485 certified facility gmp fda isi qci certified as applicable size half inch x 9.1 meter, containing chlorhexidine gluconate 2 percent weight by volume and ethanol 80 percent volume by volume with dispenser gmp fda isi qci certified as applicable size 500 ml, chlorhexidine scrub chg 4 percent with emollient and moisturizer gmp fda isi qci certified as applicable size 500 ml, chlorhexidine scrub chg 4 percent with emollient and moisturizer gmp fda isi qci certified as applicable size 500 ml, waterless foam based chg and alcohol based hand rub for hand hygiene formulated with chlorhexidine gluconate ip 2.5 percent volume by volume equivalent to 0.5 percent weight by volume chlorhexidine gluconate and ethanol ip 70 percent volume by volume with moisturizer and emollients with unique drip resistant dispenser design broad spectrum antimicrobial size 500 ml bottle, waterless foam based chg and alcohol based hand rub for hand hygiene formulated with chlorhexidine gluconate ip 2.5 percent volume by volume equivalent to 0.5 percent weight by volume chlorhexidine gluconate and ethanol ip 70 percent volume by volume with moisturizer and emollients with unique drip resistant dispenser design broad spectrum antimicrobial size 100 ml bottle, gamma sterile human dehydrated amnion chorion allograft with polyhexamethylene biguanide. size: 12 cm x 6 cm & 11 cm x 7 cm, gamma sterile human dehydrated amnion chorion allograft with polyhexamethylene biguanide. size: 8 cm x 6 cm / 7 cm x 7 cm / 5 cm x 5 cm / 3 cm x 3 cm, gamma sterile human dehydrated amnion chorion powder with 2 percent polyhexamethylene biguanide size 6 gram powder or 3 gram powder, benzydamine oromucosal spray bp nono technology (instant oral pain reliver) 30 ml (with meter dose and usfda bottel with aerosole effect), lidocaine spray 10 percent weight by volume nano technology instant local anaesthetic size 30 ml with metered dose and usfda bottle with aerosol effect, saliva suppliment mouth spray nono technology (instant e-saliva spray) 30 ml(with meter dose and usfda bottel with aerosole effect), convective patient warming system (two speed fan motor and two levels of flow rates.) can inflate a very large blanket as well as a small blanket.•uses a dc motor, quieter and state of the art blower.•warmer is controlled and operated through a unique robust software developed by care essentials.•designed to be user friendly.•comply with all essential regulatory standards. we have fda, ce, tga, japan health approvals. cws 5000 has been tested for iec 60601-1 3rd edition, am 1 by ul, usa.•warranty 1 yearelectrical supply voltage - 230-240 vacsupply frequency 50 hz classification applied part classification/device classification type bftga - medical devices & mdd 93/42/eec class ii b device performance temperature settings measure the average air temperature at the end of the delivery hose. 34°c, 37°c, 40°c, 43°c or 46°ctemperature accuracy of delivery air, except for the ambient temperature setting. ambient, +2°c with delivery hose cover physical dimensions - 29cm x 22cm x 40cmweight – 6.5 kgfilter type/life - bacteriological hepa filter/1000 hours 0.2 micron (eu-ce & us-fda approved), sterile, soft, elongated cuff having epiglottic fins with second seal for gastric access to maintain patency of drain tube with anatomically shaped lma evolution curve and fixation tab. has bite block.available with gastric access even in neonatal size starting from 1, 1.5, 2, 2.5, 3, 4, 5. delivers oropharyngeal leak pressure up to 37 cm h2o and airform elongated cuffs can be inflated to a maximum of 60cm h2o intracuff pressure (eu-ce and usfda approved), complete intubating lma set for one hand blind insertion containing lma fastrach with dedicated intubating et tube and stabilizer rod, reusable up to 40 times. requiring interdental gap of only 20mmlma fastrach is available in size 3,4,5 with intubating et tube having size ranging from 6,6.5, 7, 7.5, 8 cuffs can be inflated to a maximum of 60cm h2o intracuff pressure (eu-ce and usfda approved), ultrasonic surgical system should have the energy output for cutting and coagulation through a variety of modes which can be selected arbitrarily to meet surgical needs with reliable sealing vessels up to 5mm in diameter.generator can simultaneously monitor signals from the shears and adjust energy output according to different tissues., hand activated curved coagulating shear with next generation adaptive tissue technology with regulated power delivery for improved thermal management & a finer, non-stick coated blade, shaft compatible with 5 mm trocars, 23cm long, capable of sealing blood vessels up to 7 mm in diameter in advanced hemostasis mode, ergonomic handle compatible with generator installed in institute. european ce and usfda approved, hand activated curved coagulating shear with next generation adaptive tissue technology with regulated power delivery for improved thermal management & a finer, non-stick coated blade, shaft compatible with 5 mm trocars, 23cm long, ergonomic handle compatible compatible with generator installed in institute.european ce and usfda approved, hand activated curved coagulating shear with next generation adaptive tissue technology with regulated power delivery for improved thermal management & a finer, non-stick coated blade, shaft compatible with 5 mm trocars, 36cm long, capable of sealing blood vessels up to 7 mm in diameter in advanced hemostasis mode, ergonomic handle compatible with the compatible with generator installed in institute.european ce and usfda approved, hand activated curved coagulating shear with next generation adaptive tissue technology with regulated power delivery for improved thermal management & a finer, non-stick coated blade, shaft compatible with 5 mm trocars, 45cm long, capable of sealing blood vessels up to 7 mm in diameter in advanced hemostasis mode, ergonomic handle compatible with the compatible with generator installed in institute. european ce and usfda approved, hand activated curved coagulating shear with next generation adaptive tissue technology with regulated power delivery for improved thermal management & a finer, non-stick coated blade, shaft compatible with 5 mm trocars, 36cm long, ergonomic handle.should be competible with existing installed generator at hospital. european ce and usfda approved, hand activated curved taper tip coagulating shears compatible with ultrasonic cutting and coagulation device,17cm length,16mm curved active blade capable of sealing blood vessels up to and including 5mm in diameter, with ergonomic symmetrical finger ring grip compatible with generator installed in institute.european ce and usfda approved, hand activated curved taper tip coagulating shears compatible with ultrasonic cutting and coagulation device,9cm length,16mm curved active blade capable of sealing blood vessels up to and including 5mm in diameter, with ergonomic symmetrical finger ring grip compatible with generator installed in institute,usfda & european ce approved ., handpice for lap surgery -competible with installed generator in the institute .usfda & ce approved ., handpice for open surgery -competible with installed generator in the institute .usfda & ce approved, foot switch for foot activation foot switch for foot activation of ultrasonic energy (it should be waterproof foot switch with ipx8) -01 no, noiseless hospital grade breast pump with 3.5 inches tft lcd/led colour display with electrical & battery operated with 2 year warranty. noiseless, motorized heavy duty hospital grade breast pump which can be easily cleaned for use by multiple mothers, double pump so that it is able to pump both breasts at the same time, double piston cylinder pump without vacuum loss during double pumping and pump sets with vacuum seal technology for a high safety standard, pump must have sensitive programme feature for a gentle start and for sore nipples, color screen must provide visual orientation, and the integrated stopwatch indicates the duration of pumping, it should automatically change to stimulation mode to expression mode after 2 minutes, automatic shut off mode, electrical & battery operated; integrated lithium-ion battery: battery must have 4 hours running time at full charge and 2 hours charging time, screen must have colour differentiation for stimulation and expression. orange for stimulation, green for expression. individual cycle & suction adjustment in both stimulation & expression mode. it does not have fixed cycle per minute in stimulation mode. *stimulation mode: 30 – 150 mbar (22 to 113 mmhg); 72 – 120 cycles / minute *expression mode: 30 – 330 mbar (22 to 250 mmhg); 30 – 60 cycles / minute. its weight should be less than 4 kgs. noise level must be around 50 db or less than <60db, it should be european ce & usfda & valid cdsco license., reusable double pump sets breast shell 26 mm, lip valve, flexible membrane pot, adapter tube cover, tube connector, bottle (120/150ml/240ml), it should be pp, bpa free bottels., personal use electric brestpump wearable individually adjustable with four different mode, each with 15 vacuum step- for maximum comfor and optimal milk flow/ max vacuum-350mbar/260mmhg & max.cycles:135/min/ it should free from bpa & bps- for the babys health. complaince with who, capacity of 180ml, 1200mah bettery short charging time in 2 hurs, ram cannula is a specialized, soft nasal cannula designed for preterm/term neonates and infants to deliver low or high-flow oxygen, as well as non-invasive respiratory support (ncpap, nippv). it features flexible, curved prongs intended to minimize nasal trauma and is colour-coded for precise, smaller sizing, offering a gentle alternative to traditional nasal prongs. (all size / all colour), pediatric hemodialysis catheters in 6.5 fr and 8.5 fr are specialized, small-caliber, dual-lumen catheters designed for acute, temporary, or chronic dialysis in infants and children. length 10 cm - 12 cm, pediatric hemodialysis catheters in 10 fr are specialized, small-caliber, dual-lumen catheters designed for acute, temporary, or chronic dialysis in infants and children. length 10 cm - 15 cm, haemolock uterine balloon t onade is a sterile single use 24 fr 100 percent silicone device intended for the management of postpartum hemorrhage pph by applying pressure to the uterine walls, manual vacuum aspiration (mva) kits are handheld, reusable medical devices designed for uterine aspiration, typically featuring a 60cc double-valve polypropylene syringe that generates a vacuum of 24–26 inches of mercury (hg). kits commonly include 8 assorted flexible or rigid karman cannulae (sizes 4–12 mm), silicone oil, and are autoclavable, with a reusable lifespan of 25–50 uses., for level 4 protection viral barrier medium size gown, disposable bag, plain sheet large, 1 pair waterproof legging, 1 pair legging nw, head & eye shield, paper hand towel. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, skin marker pen for thick marking. level 1 protection as per ansi / aami standard / iso 13485-2016 made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, for abdominal & spinal surgery major drap size : 1.6x2.5m incise drap 15x35cm. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, for all kind of laparoscopy surgery set size : 1.5x2.5m., apearture 30x35cm., adhesive around apearture, 4 pockets 15x35cm., 5 tube & cable holders, polysheet lining 1.20x1.20 mtr. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, c arm cover in 2 pieces transparent natural colour cover. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, radio opaque types have blue polypropylene with bariun sulphate thread bonded with the patties size : 5 x 5mm. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, full gown eco with fluba cuff saves you from deadly diseases such hiv and hepatitis c by preventing passage of patients fluid to other side of cuff. 48-52 gsm sms fabric, height 140 cm, width 70mm, sleeve : 60 cm, hydro head : 450mm wc, total weight : 195 gram. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape overing the drums. level 4 protection as per ansi / aami standard / iso 13485-2016, bilateral knee surgery polymer sheet over all size : 240x320 cm., work pad size : 120x100 cm., elastic holes 2 nos. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape overing the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, for all kind of surgery in knee and knee replacement over all size : 240x340cm, elastic aperture 5cm dia, 2 pockets 10x35cm., 2 tube & cable holders c arm cover 70x85cm, absorbent work pads 50x10cm (2nos.), poly sheet lining 120x120cm. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, for all kind of surgery in hip area including hip replacement head sheet size : 2.0x2.4m, adhesive strip 4cm x 1.5m, 2 pockets 12x35cm., 2 tube & cable holders 30x50cm, u sheet size : 1.75x2.40m, u cut : 2cm x 20cm, straight 24 cm round, absorbent work pads 50x10cm (2nos.), poly sheet lining 1.20x1.25m. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, for all kind of surgery in shoulder area including shoulder replacement head sheet size : 1.25x1.6m, adhesive strip 4cm x 1.5m, u sheet 2x1.5m, u cut 2cm x 15cm straight 16cm round, 2 tube & cable holders, absorbent work pads 50x10cm (2nos.), poly sheet lining 1.2x1.2m. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. level 1 protection as per ansi / aami standard / iso 13485-2016, for endoscopic surgery in keen joint over all size: 150x280cm, elastic aperture 5cm dia, plastic film funnel 80cm perimeter 60cm depth. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. level 1 protection as per ansi / aami standard / iso 13485-2016, for endoscopic surgery in shoulder joint over all size : 160x190cm 1 sheets, 160x210cm 1 sheets, plastic film funnel1 90 cm and 70cm height with adhesive nozzle and bendable wires qty 2 funnels. level 1 protection as per ansi / aami standard / iso 13485-2016, operating miscroscope drape with three pair eye lens cover size : 125x200cm. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, plain sheet (large) 25 micron thick pe hygiene film made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, video camera cover & cable cover size :15cm x 250 cm made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, for cesarean section (per abdominal delivery of baby), sheet size : 1.5x2.5m. with funnel, incision area : 24cm diameter, 1tube & cable holder, polysheet lining 1.2x1.2m. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, for all kind of gynecological surgery, sheet size : 1.5x1.6m., apearture size : 13x20cm., adhesive around apearture, 2 leggings attached to main sheet, 2tube & cable holder. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016, transparent natural colour cling film. made of acid reacting material. on coming in contact with eto acid is neutralised and colour changes from purple to green. eto tag has to be securedly fixed to the drape covering the drums. level 1 protection as per ansi / aami standard / iso 13485-2016

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