Thromboplastin + Urine Ketone Stripthromboplastin + 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.

93265745

Tender Details

Category:
Infrastructure & Construction
Subcategory:
NULL

Important Dates

Publish Date:
21 September 2026
Submission Date:
06 October 2026
Opening Date:
30 November -0001

Financial Details

Tender Value:
₹ 0.00
EMD Value:
₹ 0.00
Document Value:
₹ 0.00

Location Information

Country:
India
State:
Kerala
City:
-
Location:
-
Address:
Pincode:
-

Contact Information

Contact Person:
-
Email:
-
Phone:
-
Fax:
-

Description

Thromboplastin + Urine Ketone Stripthromboplastin + 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). ]

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