Supply Of THROMBOPLASTIN + URINE KETONE STRIP
Tender Overview
Project Description
Supply Of thromboplastin + urine ketone strip , thromboplastin ( prothrombin time ) reagent in 5 ml bottle ( 1 ml = 5 tests) , make : tulip, agappe, erba or similar , unit : (no= bot) ] , urine ketone strip: 1.strips should be used for semi-quantitative detection of keto nes in urine. 2. quantity: 50 tests/kit. 3. urine strips should be made of disposable plastic. 4. urin e strips should be supplied in a sealed canister along with a desiccant and should be ready to use. 5. each bottle should have a high quality colour chart for accurate analysis. 6. should ha ve a short interpretation time not more than 60 seconds. 7. storage temperature:15 degree cel sius to 30 degree celsius. 8. should have a shell life of minimum 18 months. 9. lot number and ex piry date should be? printed on the canister. 10. product literature should be submitted with e ach kit. 11. the manufacturers shall have a license issued by the competent authority defined u nder drugs and cosmetics act, 1940. 12. compliance to medical device rules (mdr) 2017 as amend ed till date and should have a valid medical device license for the product. 13. in case of impor ted kits it should be registered and licensed by the dcg(i). 14. iso 13485/ icmed 13485 or equivale nt certified manufacturer. 15. availability of test report from central govt/nabl/ilac accredited lab to prove the conformity to the declared specification. (proof of the same to be submitted). ]
BOQ
| Sl. No. | Item Description |
|---|---|
| 1 | THROMBOPLASTIN ( PROTHROMBIN TIME ) REAGENT IN 5 ML BOTTLE ( 1 ML = 5 TESTS) , MAKE : TULIP, AGAPPE, ERBA OR SIMILAR , UNIT : (NO= BOT) ] |
| 2 | URINE KETONE STRIP: 1.STRIPS SHOULD BE USED FOR SEMI-QUANTITATIVE DETECTION OF KETO NES IN URINE. 2. QUANTITY: 50 TESTS/KIT. 3. URINE STRIPS SHOULD BE MADE OF DISPOSABLE PLASTIC. 4. URIN E STRIPS SHOULD BE SUPPLIED IN A SEALED CANISTER ALONG WITH A DESICCANT AND SHOULD BE READY TO USE. 5. EACH BOTTLE SHOULD HAVE A HIGH QUALITY COLOUR CHART FOR ACCURATE ANALYSIS. 6. SHOULD HA VE A SHORT INTERPRETATION TIME NOT MORE THAN 60 SECONDS. 7. STORAGE TEMPERATURE:15 DEGREE CEL SIUS TO 30 DEGREE CELSIUS. 8. SHOULD HAVE A SHELL LIFE OF MINIMUM 18 MONTHS. 9. LOT NUMBER AND EX PIRY DATE SHOULD BE? PRINTED ON THE CANISTER. 10. PRODUCT LITERATURE SHOULD BE SUBMITTED WITH E ACH KIT. 11. THE MANUFACTURERS SHALL HAVE A LICENSE ISSUED BY THE COMPETENT AUTHORITY DEFINED U NDER DRUGS AND COSMETICS ACT, 1940. 12. COMPLIANCE TO MEDICAL DEVICE RULES (MDR) 2017 AS AMEND ED TILL DATE AND SHOULD HAVE A VALID MEDICAL DEVICE LICENSE FOR THE PRODUCT. 13. IN CASE OF IMPOR TED KITS IT SHOULD BE REGISTERED AND LICENSED BY THE DCG(I). 14. ISO 13485/ ICMED 13485 OR EQUIVALE NT CERTIFIED MANUFACTURER. 15. AVAILABILITY OF TEST REPORT FROM CENTRAL GOVT/NABL/ILAC ACCREDITED LAB TO PROVE THE CONFORMITY TO THE DECLARED SPECIFICATION. (PROOF OF THE SAME TO BE SUBMITTED). ] |
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