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D-Dimer Determination Kit - India CDSCO Medical Device Registration

D-Dimer Determination Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000246_06b9210d1f4419085a19edb52036be3e_e3375ff1fbb5e134974d662d4e7bc81c. This device is marketed under the brand name HFABP. The license holder is Allied Biotechnology India 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
D-Dimer Determination Kit
UID: IMP/IVD/2022/000246_06b9210d1f4419085a19edb52036be3e_e3375ff1fbb5e134974d662d4e7bc81c

Brand Name

HFABP

Device Class

Class C

Approving Authority

CDSCO

Product Information

For quantitative detection of D-dimer in human plasma or whole blood

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