Loading…
Loading…
| # | Company | Amount | Rank | Status |
|---|---|---|---|---|
| 1 | L2₹6 L+₹11,591.50 (1262.7%)Accepted-AOC | L2 | Accepted-AOC As Per Rate Approval Letter | |
| 2 | L3₹6 L+₹14,036.50 (1529.0%)Accepted-AOC | L3 | Accepted-AOC As Per Rate Approval Letter | |
| 3 | L4₹22 L+₹16,669 (1815.8%)Accepted-AOC GREEN SPICE GIRRAJ NAGAR MANSAROVAR JAIPUR | JAIPUR | RAJASTHAN | 302001 | L4 | Accepted-AOC As Per Rate Approval Letter | |
| 4 | L5₹6 L+₹22,699 (2472.7%)Accepted-AOC | L5 | Accepted-AOC As Per Rate Approval Letter | |
| 5 | L1₹918Rejected-AOC A 332 TALWANDI KOTA | L1 | Rejected-AOC As Per Rate Approval Letter |
Tender Value
Refer Docs
EMD Value
₹40,000
Closing Date
7 Dec 2020, 4:00 pmClosed
Superintendent
Superintendent Mathuradas Mathur Hospital Jodhpur
Disposable and Chemical for Nephrology
2020_SNMCJ_206315_1
Ref no 16675 Dated 21.11.20
Open Tender
Miscellaneous Goods
Item Wise
365 days
Mathuradas Mathur Hospital Jodhpur
Please refer Tender documents.
2 documents required · 2 mandatory
₹400
Yes
Superintendent Mathuradas Mathur Hospital Jodhpur
₹40,000
Yes
Superintendent Mathuradas Mathur Hospital Jodhpur
14 Jan 2021
24 Nov 2020
8 Dec 2020
24 Nov 2020
7 Dec 2020
24 Nov 2020
27 Nov 2020
Nephrology Items
Hemoconcentrate Part A & B- A. The constituents of the hemoconcentrate are as follows: • Part-A (aqueous)-Sodium Chloride: 160-170g/L; Potassium Chloride: 5-5.5g/L, Calcium Chloride: 8.5-9g/L; Magnesium Chloride: 5-5.50g/L; Glacial Acetic Acid: 8-9g/L and QS purified water. (when diluted as 1:34) Sodium:75-85 mmol/L, Potassium: 0-2mmol/L, Calcium-1.70-1.75mmol/L, Magnesium: 0.75-1mmol/L, Chloride: 85-90mmol/L, Acetate: 3.5-4.5mmol/L. Part B- Each powder packet weighing 800-900gm containing Sodium Chloride:200-300gm, Sodium Bicarbonate: 500-650gm which provides after dissolving Sodium 55-60 mmol/L, Chloride: 20-25mmol/L; Bicarbonate: 30-40 mmol/L. (One Part A jar and Three Part B powder)
Arterio- Venous Fistula needle : one pre-sterlized set each with a pair of needles, 16 Gauze needle with back eye and length 25-30mm with fixed wings with Luer lock in the attached blood tubing of length 25-30cm. The manufacturer should have US FDA/ CE of EUROPE certificate for the product. (each twin pair set)
Dialyzer: Dialyzer for hemodialysis of adult patients which should be presterlized and reusable having synthetic hollow fibre of Polysulfone able to bear blood flow of minimum 200ml/min and dialysate flow rate of 500ml/min with surface area- 1.3-1.4m² (requirement: 100/month), which should be able to be rinsed effectively for reuse post hemodialysis. The manufacturer should provide US FDA/CE of Europe certificate of the product and model supplied. (EACH dialyzer)
Dialyzer: Dialyzer for hemodialysis of adult patients which should be presterlized and reusable having synthetic hollow fibre of Polysulfone able to bear blood flow of minimume 200ml/min and dialysate flow rate of 500ml/min with surface area-1.6 m² (requirement: 40/month) which should be able to be rinsed effectively for reuse post hemodialysis. The manufacturer should provide US FDA/CE of Europe certificate of the product and model supplied. (EACH dialyzer)
Arteriovenous line: It should be supplied with blood tubing to be attached to the dialyzer during dialysis. The length of pre sterilized latex free medical grade tubing should be 35-40cm with capacity of priming volume approximately 145-155ml with arterial chamber, venous chamber with respective arterial and venous luer locks and injection ports in the tubing and ends of the tubing fitted with suitable connectors to the access and dialyzer. The manufacturer should provide US FDA/CE of Europe certificate of the product and model supplied. (EACH tubing)
Pediatric dialyzer: The pediatric dialyzer should be pre sterilised and made of synthetic Polysulfone hollow fibre with surface area 0.6m² (requirement: 25/year), The manufacturer should provide US FDA/ CE of EUROPE certificate of the product and model supplied. The dialyzer and arteriovenous blood line of same manufacturer would be preferred. (Each dialyzer)
Pediatric dialyzer: The pediatric dialyzer should be pre sterilised and made of synthetic Polysulfone hollow fibre with surface area 0.8m² (requirement- 150/year). The manufacturer should provide US FDA/ CE of EUROPE certificate of the product and model supplied. The dialyzer and arteriovenous blood line of same manufacturer would be preferred. (Each dialyzer)
Pediatric arteriovenous line (blood tubing): The pediatric arteriovenous blood line should be pre sterilised and latex free with arterial chamber, venous chamber with respective arterial and venous luer locks and injection ports in the tubing and ends of the tubing fitted with suitable connectors to the access and dialyzer. The manufacturer should provide US FDA/ CE of EUROPE certificate of the product and model supplied. The dialyzer and arteriovenous blood line of same manufacturer would be preferred. (Each blood line)
Plasma filter for Plasmapheresis: The plasma filter for therapeutic plasmapheresis in renal failure patients pre sterilised with polysulfone/polyethylene membrane with effective surface area- 0.5m²- 0.6 m² (requirement- 100/year); surface area- 0.2m²- 0.3 m² (requirement-50/year). The manufacturer should provide US FDA/ CE of EUROPE certificate of the product and model supplied. (Each)
Double lumen catheter for Hemodialysis with Kit: The double lumen catheter for hemodialysis in patients. It should be pre sterilized, of flexible radio opaque polyurethane material make with J end guide wire, introducer needle,vessel dilator with arterial and venous port caps, syringe 5-10cc with luer lock. Catheter with preferred. Size of the double lumen catheters to be supplied are: A. 8F× 8-9cm (requirement- 50/year).The products and model supplied should be USFDA/CE of Europe certified. (one double lumen catheter with guide wire and items)
Double lumen catheter for Hemodialysis with Kit: The double lumen catheter for hemodialysis in patients. It should be pre sterilized, of flexible radio opaque polyurethane material make with J end guide wire, introducer needle,vessel dilator with arterial and venous port caps, syringe 5-10cc with luer lock. Catheter with preferred. Size of the double lumen catheters to be supplied are: B. 11.5F-12F×13-14cm (requirement- 50/month); The products and model supplied should be USFDA/CE of Europe certified. (one double lumen catheter with guide wire and items)
Long term/Chronic double lumen hemodialysis catheter with Kit: Double lumen catheter for long term/chronic hemodialysis which should be pre sterilised, of flexible radio opaque polyurethane material make with J end guide wire, pull apart sheath( which must have lock to prevent back flow of blood), dilator 12F and 14F, tunnelling stylet, scalpel, syringe with leur lock with arterial and venous port caps. Size of the catheter 14.5-15F×19cm (requirement- 30/year). The products and model supplied should be USFDA/CE of Europe certified. (Each catheter kit)
Biopsy Gun: Kidney biopsy gun with size A. 16 Gauze×16cm needle (requirement- 100/yearwith penetration depth 22mm, pre sterile, automated spring loaded. The product and model supplied should be USFDA/CE of Europe certified. (Each biopsy gun)
Biopsy Gun: Kidney biopsy gun with size 18 Gauze×16cm needle (requirement- 50/year) with penetration depth 22mm, pre sterile, automated spring loaded. The product and model supplied should be USFDA/CE of Europe certified. (Each biopsy gun)
Peritoneal dialysis catheter: Kit to include pre sterilised rigid peritoneal dialysis catheter with single cuff with metal stiletto with pointed end, scalpel with holder, connector with flow regulator. The catheter to be supplied with peritoneal dialysis fluid administration set. Peritoneal dialysis catheter with administration set (requirement- adult—200/year; (one catheter kit with administration set)
Peritoneal dialysis catheter: Kit to include pre sterilised rigid peritoneal dialysis catheter with single cuff with metal stiletto with pointed end, scalpel with holder, connector with flow regulator. The catheter to be supplied with peritoneal dialysis fluid administration set. Peritoneal dialysis catheter with administration set (requirement-; pediatric-50/year). (one catheter kit with administration set)
High Concentrate Part A Hemodialysis Solution 1. High Concentrate A HD Solution compatible with dry bag part B powder. Company must be ISO & GMP Certified. 2. Fluid composition: Sodium 103 mmol/L, Chloride 109.5 mmol/L, Calcium 1.75 mmol/L, Magnesium 0.5 mmol/L, Potassium 2mmol/L Presence of glucose in HD fluid solution is optional. (Per Liter)
Citrosteril- 5 litre cans. (Each Can)
6% sodium hypochlorite- 5 litre cans (Each Can)
Acetic acid glacial- 5 litre cans (Each Can)
Citric acid monohydrate 500gm.
Hydrochloric acid- 5 litre cans (Each Can)
Cap Tacrolimus- 0.5 mg (each tablet)
Cap Tacrolimus-1.0 mg (each tablet)
Cap Tacrolimus-2 mg (each tablet)
Tab Mycophenolate Sodium enteric coated tablets – 180 mg (each tablet)
Tab Mycophenolate Sodium enteric coated tablets – 360 mg (each tablet)
Injection of Basiliximab 20 Mg (each vial)
Rabbit antithymoglobulin 250 Mg (each vial)
Cap Valganciclovir 450 Mg (each tablet)
Injection cefepime 1.1 gm + Tazobaetum (each vial)
HTK Solution for Transplatation (2 Liter)
HTK Solution for Transplatation (1 Liter)
AORTIC PUNCH for Transplatation (5 mm)
AORTIC PUNCH for Transplatation (3 mm)
0.9% N S (Glass bottle) (100 ml)
0.45% N S (Glass bottle) (500 ml)
0.9% N S (Glass bottle) (500 ml)
0.9% N S (Double layered Packing) (1 Litre)
hope health care
S.R.PHARMA
navlaxmi pharma
Rapid Healthcare
S.R.PHARMA
hope health care
navlaxmi pharma
stage.html
html • 0.06 MB
tech_bid_open.pdf
tech_eval.pdf
fin_bid_open.pdf
boq_comp_chart.xlsx
xlsx
fin_eval.pdf
aoc.pdf
Tap a document below to read it instantly. You can also download everything as a ZIP if you prefer.
details.html
html • 0.03 MB
Download all tender documents and submit your bid
Disclaimer: TenderKart has made every reasonable effort to ensure that the information on this page is accurate and authentic, however it cannot be held liable for any third-party claims or losses or any damages. TenderKart makes no warranty, expressed or implied, as to the results obtained from the use of this information. If you notice any error or omission, please let us know at .