tender for thromboplastin + urine ketone strip, 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).

You can fill out the integrated inquiry form below on this detail page to share your company profile. Our consultancy desk will review your query regarding medical device parameters and guide you on how to coordinate efficiently with the procurement team of Southern Railway SR

Tender18 provides end-to-end professional bidding support and documentation advisory for Tender For Thromboplastin + Urine Ketone Strip, 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). . Our senior analysts help you decode the complete project guidelines, manage accurate costing sheets, and complete error-free submissions on the official platform used by Southern Railway SR.

Most online bids face rejection during the initial evaluation round due to avoidable errors like uploading blurred document scans, submitting expired DSCs, or missing critical experience papers required for Tender For Thromboplastin + Urine Ketone Strip, 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). in Kerala.

Eligibility for outstation bidders depends entirely on the terms set inside the document for Tender For Thromboplastin + Urine Ketone Strip, 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).. While many public sector projects allow national competitive bidding, certain localized works require local offices or specific registration metrics in Trivandrum.

If this procurement is routed through the central marketplace, an active GeM Seller ID is mandatory to supply medical device items. Tender18 offers complete assistance for brand cataloging, profile creation, and vendor assessment required officially by Southern Railway SR

To register an eligible bid for these medical device contracts, companies must prepare their core compliance documents. Vendors operating across Kerala must ensure they possess a valid GST registration, permanent account number (PAN), and active Class-3 Digital Signature Certificates.

This public procurement cycle is specifically looking for qualified vendors and suppliers who can provide high-quality medical device solutions. The operational execution, delivery, and deployment of these materials must be managed locally within the Trivandrum region.

The estimated project cost and budget thresholds can be reviewed directly inside the tender document. Bidders can analyze these qualification files to check if their firm meets the financial capability criteria specified for Tender For Thromboplastin + Urine Ketone Strip, 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). by Southern Railway SR

You can download the commercial Bill of Quantities (BOQ) spreadsheet directly using the secure link provided on this page. The BOQ file contains the item descriptions and rate filling forms officially validated for Tender For Thromboplastin + Urine Ketone Strip, 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). within the Kerala jurisdiction

The official timeline and deadline details for Tender For Thromboplastin + Urine Ketone Strip, 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). are available inside the detailed notification files. Bidders planning to target this contract in Trivandrum should check the official portal schedule early to complete their online technical and financial submission well before the closing hours.