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Tender For srphc82281210-coronary drug eluting stents (1) single wire technology on cobalt based alloy platform (2) stent with coating of biolinx polymer carrier for active drug zotarolimus shown to be effective in preventing neo-intimal hyperplasia) (3) stent diameter should be from 2.25 mm to 4 mm and length of the stent from 12mm to 38 mm. (4) the strut thickness should be 81 micron or less. (5) stent delivery system should be monorail (single operator exchange or rapid exchange). (6) stent should be compatible with 5fr guiding catheter (7) stent design should be open cell type. (8) stent should be approved by dcgi. the copy of dcgi approval should be enclosed in the tender bid. (9) five years long term efficacy and safety of the stent in terms of target vesselrevascularisation (tvr) and in-situ thrombosis (ist) should be documented / published inpeer reviewed scientific journals.(10) the documents pertaining to the efficacy and safety of the stent should be enclosed for the brand that is offered in the tender bid (11) the manufacturer/supplier should submit proof of supply of the stent to a major government institute.[quantity tolerance (+/-): 5 %age , item category : normal , total po value variation permitted: max 8 lacs ] ]
Tender For srphc82281275-des-abbreviated dapt long -coronary drug eluting stents with (1) platinum chromium alloy (2) coating of bioabsorbable polymer carrier for activedrug everolimus shown to be effective in preventing neo-intimal hyperplasia) (3) stent diameter should be from 2.5mm to 4mm. the length of the stent should be from 12mm to 48 mm. (4) the strut thickness should be 91 micron or less. (5) stent delivery system should be monorail (single operator exchange or rapid exchange). (6) stent should be compatible with 5fr guiding catheter (7) stent design should be open cell type. (8) stent should be approved by dcgi. the copy of dcgi approval should be enclosed in the tender bid. (9) the long term efficacy and safety of the stent, the rates of in-stent restenosis (isr) and in-situ thrombosis (ist) should be documented / published in peer reviewed scientific journals. (10) safety of abbreviated (three month) dual antiplatelet therapy for high bleeding risk patients should be documented in peer reviewed journals. (11) the manufacturer/supplier should submit proof of supply of the stent to a major government institute. bis standards for the drug eluting stent are not available. (reference:bis catalogue ).[quantity tolerance (+/-): 5 %age , item category : normal , total po value variation permitted: max 8 lacs ] ]
Tender For srphc82281225-coronary drug eluting stents with (1) cobalt chromium alloy (2) coating of bioabsorbable polymer carrier with abluminal and gradient coating foractive drug shown to be effective in preventing neo-intimal hyperplasia) (3) stent diameter should be from 2.5mm to 4mm . the length of the stent should be from 12mm to 38 mm. (4) the strut thickness should be 91 micron or less. (5) stent delivery system should bemonorail (single operator exchange or rapid exchange). (6) stent should be compatible with 5fr guiding catheter (7) stent design should be open cell type. (8) stent should be approved by dcgi. the copy of dcgi approval should be enclosed in the tender bid. (9) the long term efficacy and safety of the stent, the rates of in-stent restenosis (isr) and in-situ thrombosis (ist) should be documented / published in peer reviewed scientific journals. (10) safety of abbreviated (one month) dual antiplatelet therapy for high bleedingrisk patients should be documented in peer reviewed journals. (11) the manufacturer/supplier should submit proof of supply of the stent to a major government institute. bis standards for the drug eluting stent are not available. (reference:bis catalogue ).[quantity tolerance (+/-): 5 %age , item category : normal , total po value variation permitted: max 8 lacs ] ]
Tender For srphc82281280-des-pt/cr : coronary drug eluting stents (1) on platinum chromium platform (2) stent with coating of polymer carrier for active drug everolimus shown to be effective in preventing neo-intimal hyperplasia) (3) stent diameter shouldbe from 2.5mm to 4mm and length of the stent from 12mm to 38 mm. (4) the strutthickness should be 91 micron or less. (5) stent delivery system should be monorail (single operator exchange or rapid exchange). (6) stent should be compatible with 5fr guiding catheter (7) stent design should be open cell type. (8) stent should be approved bydcgi . the copy of dcgi approval should be enclosed in the tender bid. (9) the long termefficacy and safety of the stent in terms of target vessel revascularisation (tvr) and in-situ thrombosis (ist) should be documented / published in peer reviewed scientific journals.(10) the documents pertaining to the efficacy and safety of the stent should be enclosed for the brand that is offered in the tender bid (11) the manufacturer/supplier should submit proof of supply of the stent to a major government institute.[quantity tolerance (+/-): 5 %age , item category : normal , total po value variation permitted: max 8 lacs ] ]
Tender For corrigendum : e-bid for rate contract cum supply and empanelment of surgical items - hand activated curved taper tip coagulating shears compatible with ultrasonic cutting and coagulation device,9cm length,16mm curved active blade with adaptive tissue technology capable of sealing blood vessels up to and including 5mm in diameter, with ergonomic symmetrical finger ring grip-focus 9, hand activated curved taper tip coagulating shears compatible with ultrasonic cutting and coagulation device,17cm length,16mm curved active blade with adaptive tissue technology capable of sealing blood vessels upto and including 5mm in diameter, with ergonomic symmetrical finger ring grip- focus 17, double wall resuscitator with peep valve in paediatricsit should be fully autoclavable double wall with hand strapit should be supplied with autoclavable reservoir bag it should have a singleshutter valve system made of silicone rubberit should have easy attachment of peep valve for peadiatricit should have provision to attach manometer for paediatrics ambu bagbag volume: mark iv baby (300 ml)weight: baby (190 g)it should be us-fda, ce & iso certified, ultrasorbs ap disposable drypads,dry pad for moisture management, 58.4x90cm, with breathable layer, super absorbent core, aqua shield film and air permeable back sheet, absorbency of 1800- 2300gm, usfda/ce/biscompliant, iso13485 compliant, volumetric incentive spirometer (adult) volumetric incentive spirometer (adult) 4000 ml with handle. volume measurement must be compact comfortable designed to accommodate large inspired volumes. must have good-better-best flow window & advanced, low work-of-breathing design.particulate filter screen in device housing must help to reduce risk of foreign matter passing to patients.expandable and collapsible tube must help patients find comfortable position for treatments and can be removed when storing the device. ergonomic swiveled mouthpiece allows to patients create tight seal to enable more accurate measurement. flow indicator with smiley face provides visual target for desired inhalation and bright green flow indicator make it easy for patients to see results. manufacturer must be us-fda registered & certified with en/eu iso 13485 & applicable 510k &ce certification., neonatal high flow cannula having 8 litreflow. it can also be used for hfnc + nippv/cpap. should have a soft tip., pur-xro catheter 20 cm, 28g/1fr picc line with stylet, splitting needle with securing wings with 8cm extension tubing ( flow rate 0.7ml/min)., pur-xro catheter 30 cm, 24g/2fr picc line with split cannula and 10cm extension tubing over catheter (flow rate 4.5ml/min)., silicone foleys catheter with three noble metal alloy coating consisting of gold, silver & palladium (coated internally & externally surfaces), silicone foleys catheter with three noble metal alloy coating consisting of gold, silver & palladium (coated internally & externally surfaces), silicone foleys catheter with three noble metal alloy coating consisting of gold, silver & palladium (coated internally & externally surfaces), long term double lumen dialysis catheter with kit accessories should be provided ( catheter,pull apart sheath, dialator, tunneling stylet,guide wire j/s,with disppencer and injection caps, symmetrical tip retrograde and antigrade long term double lumen dialysis catheter size 15 fr x 23 cmusfda certification, "sterile disposable perfusion set (infusion set) with airway and needle (paediatric use) burette type measured volume chamber of 100 ml drop size of approx 60 drops per ml injection port,latexfree, for intermittent medication. floating auto shut off valve (latex free) in burette. soft and kink resistant pvc tubing. roller controller for flow control tube length 150 cm 23g needle as per iso 8536-5", "plaster of paris bandages 15cm x 2.7mts / roll testing parameter should befollowed as per bp standard", urine collecting bag, disposable 2000 ml transparent sh
Tender For corrigendum : supply of capd fluids for dialysis with all accessories required in dialysis process - transfer set for capd fluid a transfer set for capd is a tubing system that connects the patients peritoneal dialysis catheter to the external dialysis fluid pipeline allowing for the flow of dialysate into and out of the peritoneal cavity for waste removal these sets are crucial for the effectiveness and safety of capd which is a home dialysis treatment for end stage renal disease they are desingned to ensure a secure aseptic connection and include components like clamps and connectors , non sterile cycler drain bag 15 ltr capacity is 15 liters , capd simple disconnect set 3 ltr capacity is 3 liters , pd cassete set with 4 prong pd set with cassete pack of 50 sets each featuring a 4 prong cassette , minicap f capd