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Blood Collection Tube - K2 EDTA - India CDSCO Medical Device Registration

Blood Collection Tube - K2 EDTA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000154_2ffa9e811a315fac149a9b13733e48ff_73af9142f1749c28f7bdc1e3110dd403. This device is marketed under the brand name KRIVIDA - Vacuum Sodium Heparin. The license holder is GAMMA AGRO-MEDICAL PROCESSINGS PVT.LTD, and it is classified as Device Class Class A. The approving authority is Telangana.

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CDSCO Registered
Class Class A
Blood Collection Tube - K2 EDTA
UID: MFG/IVD/2022/000154_2ffa9e811a315fac149a9b13733e48ff_73af9142f1749c28f7bdc1e3110dd403

Brand Name

KRIVIDA - Vacuum Sodium Heparin

Device Class

Class A

Approving Authority

Telangana

Product Information

A sterile plastic tube, sealed with a stopper, containing a pre-measured amount of vacuum and the anticoagulant dipotassium ethylene diamine tetraacetic acid (KRIVIDA - Vacuum Sodium Heparin). It is intended to be used for the collection, and preservation and/or transport, of blood for analysis and/or other investigation [e.g., blood lead, whole blood haematology such as complete blood count (KRIVIDA - Vacuum Sodium Heparin), molecular diagnostics, and immunohematology testing (KRIVIDA - Vacuum Sodium Heparin)]. This is a single-use device

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