ABO test cell reagents of human origin in a buffered suspension medium at 0.8 single vial A1 1 x 10 mL, Id-n 06012, 200 Tests.
Other Specifications Download Specification | |
---|---|
Conformity To Indian Standard | IS:9824(Part-3) Latest |
ISI Marked | Yes |
CM/L No | 3852 |
Type Of IV Set | Transfusion Set for Single Use (Designation : Transfusion Set IS 9824-3 TS) |
Transfusion/Infusion Set Provided With Injection Site | No |
Provision Of Closure Of Air Inlet With Vented Infusion Set | No |
Air Inlet Device With Air Filter Required | No |
Luer Lock Fitting | No |
I V Set Comply With The Provisions Of Drugs And Cosmatic Act 1940 As Amended Till Date | Yes |
Good Manufacturing Practices (GMP) Issued Under Revised Schedule -M Of Drugs And Cosmetics Act 1940 As Amended Or WHO-Good Manufacturing Practices (GMP)(For Manufacturers Only) | Yes |
Good Manufacturing Practices (GMP) Certificate No. | 5487 |
Good Manufacturing Practices (GMP) Certificate Date | 21-06-2016 |
Non Conviction Certificate Issued By The Concerned Drugs Control Authorities/ Licencing Authorities | Yes |
Non Conviction Certificate No. | 87215 |
Non Conviction Certificate Date | 05-09-2017 |
Availability Of Test Reports From Drug Controller Approved Laboratories Which Are Also Satisfying Central Govt./State Govt/NABL/IL AC Accredited Lab Covering All The Declared Parameters As Per IS Specification | Yes |
Test Report No | NA |
Test Report Date | NA |
Name Of The Lab | NA |
Address Of The Lab | NA |