Blood Collection Tube - K3 EDTA - India CDSCO Medical Device Registration

Blood Collection Tube - K3 EDTA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000154_9b4956e840ec193827dba8b1a8237e23_319b022c70367f1ff7419ae96caac128. 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 - K3 EDTA

UID: MFG/IVD/2022/000154_9b4956e840ec193827dba8b1a8237e23_319b022c70367f1ff7419ae96caac128

Brand Name

KRIVIDA - Vacuum Sodium Heparin

License Holder

GAMMA AGRO-MEDICAL PROCESSINGS PVT.LTD

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 tripotassium ethylene diamine tetraacetic acid (KRIVIDA - Vacuum Sodium Heparin). It is intended to be used for the collection, preservation and/or transport, of blood for analysis and/or other investigation [e.g., whole blood haematology such as complete blood count (KRIVIDA - Vacuum Sodium Heparin), and quantitative drug assay determinations]. This is a single-use device

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Blood Collection Tube - Rapid Clot Activator

Brand: KRIVIDA - Vacuum Sodium Heparin

GAMMA AGRO-MEDICAL PROCESSINGS PVT.LTD

Blood Collection Tube - K3 EDTA - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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