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Alpha Feto Protein Enzyme Conjugate Reagent - India CDSCO Medical Device Registration

Alpha Feto Protein Enzyme Conjugate Reagent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000078_f7c4d69c717edac2f62d4a65377a5688_a7b6e645a5dd0e880a8114b225786565. This device is marketed under the brand name AFP+CEA+PSA. The license holder is Tosoh India Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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
Alpha Feto Protein Enzyme Conjugate Reagent
UID: MFG/IVD/2021/000078_f7c4d69c717edac2f62d4a65377a5688_a7b6e645a5dd0e880a8114b225786565

Brand Name

AFP+CEA+PSA

License Holder

Tosoh India Pvt. Ltd.

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

For in-vitro diagnostic use only for quantitative determination of Alpha Feto Protein (AFP+CEA+PSA) in Human Serum by a Microplate Enzyme Immunoassay (AFP+CEA+PSA)

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