EVACUATED CLOSED BLOOD COLLECTION TUBES

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 ISO 13485 and US-FDA /European CE approved. Product code should be mentioned which is quoted and supplied to the institution. • It should be Gamma sterile /EB as per current ISO11137 guidelines. • Batch wise sterility, Pyrogenicity and Toxicity certificate should be given.

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 3.0 ml(5.4 mg), volume capacity. • Batch wise sterility, Pyrogenicity and Toxicity certificate should be given • It should be ISO 13485 and US-FDA /European CE approved. Product code should be mentioned which is quoted and supplied to the institution. • It should be Gamma sterile /EB as per current ISO11137 guidelines.

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 hemogard, 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 ISO 13485 and US-FDA /European CE approved. Product code should be mentioned which is quoted and supplied to the institution. • It should be Gamma sterile /EB as per current ISO11137 guidelines.

4) Evacuated Tube for Silica-clot activator/silicon coated made of clear latex polyethylene terephthalate with hemogard 13 mm x 75 mm, Vol. 4.0 ml. o It should be ISO 13485 and US-FDA/European CE approved. Product code should be mentioned which is quoted and supplied to the institution. o It should be Gamma sterile /EB 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.

5) Blood Collection needle 21 or 22 gauge with cap and safety lock for evacuated tube. • It should be ISO 13485 and US-FDA /European CE approved. Product code should be mentioned which is quoted and supplied to the institution. • It should be Gamma sterile/EB as per current ISO11137 guidelines. • Batch wise sterility, Pyrogenicity, Toxicity certificate should be given. • It should have facility to lock the needle to reduce needle stick injuries and help in one handed use. • As per CLSI recommendation it should be From Same Manufacturer of Vacuumed blood collection tube and holder.

6) Evacuated Tube for spray coated with Sodium Fluoride (3mg.), Na2EDTA (6mg.) made of clear latex polyethylene terephthalate with hemogard 13 mm x 75 mm, Vol. 2.0 ml. • It should be ISO 13485 and US-FDA/European CE approved. Product code should be mentioned which is quoted and supplied to the institution. It should be Gamma sterile /EB as per current ISO11137 guidelines. • Batch wise sterility, Pyrogenicity and Toxicity certificate should be given.

7) Evacuated Tube Needle Holder with disposable release button • It should be ISO 13485 and US-FDA/European CE approved. Product code should be mentioned which is quoted and supplied to the institution. • It should be Gamma sterile /EB as per current ISO11137 guidelines. • It should have release button to dispose the needle automatically. • As per CLSI recommendation it should be From Same Manufacturer of Vacuumed blood collection tube and holder.

8) Blood Lancet for high blood flow. • Medical Grade, stainless steel and polymer blood lancet, super sharp tip for instant incision. Sterile and individually pee label pouch pack. • Needle gauge and Depth (mm) should be at least 23G x 1.8 mm. • Blood volume should be 100 – 250µl. • Batch wise sterility, Pyrogenicity and Toxicity certificate should be given. o It should be ISO 13485 and US-FDA /European CE approved. Product code should be mentioned which is quoted and supplied to the institution It should be Gamma sterile as per current ISO11137 guidelines.