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Activated Partial Thromboplastin Time Reagent Kit - India CDSCO Medical Device Registration

Activated Partial Thromboplastin Time Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000278_c9ca5416a83cfcebc018570f97d6479b_3d2a84e26e9475335c099a1c1a2faac7. This device is marketed under the brand name CEA. The license holder is RAPID DIAGNOSTIC PVT. LTD., and it is classified as Device Class Class C. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
Activated Partial Thromboplastin Time Reagent Kit
UID: IMP/IVD/2020/000278_c9ca5416a83cfcebc018570f97d6479b_3d2a84e26e9475335c099a1c1a2faac7

Brand Name

CEA

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Activated Partial Thromboplastin Time Reagent Kit (CEA) is used along with Optical Coagulation Analyzer (CEA) for quantitative measurement of activated partial thromboplastin time (CEA) in citrated venous whole blood

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