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💬 Talk to Our Bidding ExpertCorrigendum Evacuated Closed in Udaipur - Complete Tender Details
Find eligibility criteria, important deadlines, bidding requirements, and download official documents for "Corrigendum Evacuated Closed" in Udaipur, India.
NTID 44413133
- Opening Date : Thu 16th April, 2026
- Closing Date : Wed 15th April, 2026
- ₹ 0.00
- NTID 44413133
Key Values: Document Cost: 2000.00 | EMD: 500000.00 | Estimated Cost: 0.00
Tender Description
Corrigendum : Evacuated Closed Blood Collection Tubes
Documents
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Document-1
721.3 kBOil_India_ExtraDoc...Oil_India_ExtraDocument-GCO0449P23.pdf
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Document-2
721.3 kBOil_India_ExtraDoc...Oil_India_ExtraDocument-GCO0449P23.pdf
Costs
-
EMD
500000.00 -
Document Cost
2000.00 -
Estimated Cost
Refer Documents
Latest Corrigendum List
| # | Corrigendum Title | Corrigendum Type |
|---|---|---|
| 1 | date corrrigendum | Date |
BOQ Items Total Items : 9 | Total Qty : 8
| # | Item | Quantity | Units |
|---|---|---|---|
| 1 | EVACUATED CLOSED BLOOD COLLECTION TUBES :- | ||
| 2 | 1. Clot Activator for serum with Gel 3.5 ml, 13 x 75mm with yellow cap Should be sterile, evacuated and PET and single hand operation for capping and decapping. It should be recommended of therapeutic drug monitoring. It should be US-FDA/BIS approved and should comply with the current FDA Quality System Regulation 21CFR820. Product code should be mentioned which is quoted and supplied to the institution. It should be Gamma sterile as per current ISO11137 guidelines. Batch wise sterility, Pyrogenicity and Toxicity certificate should be given. | 1.00 | Each |
| 3 | 2. Evacuated Blood Collection Tube with spray dried K2EDTA with lavender cap It should be made of clear latex free polyethylene terephthalate. Size 13 x 75 mm with 3.0ml(5.4 mg), volume capacity. Batch wise sterility, Pyrogenicity and Toxicity certificate should be given It should be US-FDA/BIS approved and should comply with the current FDA Quality System Regulation 21CFR820. Product code should be mentioned which is quoted and supplied to the institution. It should be Gamma sterile as per current ISO11137 guidelines. | 1.00 | Each |
| 4 | 3. Sodium Citrate Evacuated tube with Tube-in-Tube Technology sealed from the top to avoid citrate leakage for coagulation test with vacuum (with Na citrate - 0.109 MI ,3.2%) It should be made of clear latex free polyethylene terephthalate with light blue cap, 13 mm x 75mm Vol. 2.7 ml. Batch wise sterility, Pyrogenicity and Toxicity certificate should be given. It should have Tube-in-Tube Technology for Full Draw Volume that reduced headspace thereby minimize platelet activation and provide accurate APPT result It should be US-FDA/BIS approved and should comply with the current FDA Quality System Regulation 21CFR820. Product code should be mentioned which is quoted and supplied to the institution. It should be Gamma sterile as per current ISO11137 guidelines. | 1.00 | Each |
| 5 | 4. Evacuated Tube for Silica-clot activator/silicon coated made of clear latex polyethylene terephthalate with red cap 13 mm x 75 mm, Vol. 4.0 ml. It should be US-FDA/BIS approved and should comply with the current FDA Quality System Regulation 21CFR820. Product code should be mentioned which is quoted and supplied to the institution. It should be Gamma sterile as per current ISO11137 guidelines. Batch wise sterility, Pyrogenicity and Toxicity certificate should be given Adequate combustion data to prove that it is safe for the environment upon incineration. | 1.00 | Each |
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