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ELISA Kit for detection of Alpha-Fetoprotein in Human serum/plasma - India CDSCO Medical Device Registration

ELISA Kit for detection of Alpha-Fetoprotein in Human serum/plasma is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000068_e834543616f567b0c960ba07c1c4405a_4befc5fd6dab960972bee76787dcf222. This device is marketed under the brand name Cassette format. The license holder is Biogenix Inc. Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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
ELISA Kit for detection of Alpha-Fetoprotein in Human serum/plasma
UID: MFG/IVD/2020/000068_e834543616f567b0c960ba07c1c4405a_4befc5fd6dab960972bee76787dcf222

Brand Name

Cassette format

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Maternal Serum Alpha-Fetoprotein (Cassette format) Test reagents/kits for is a medical device intended for the spina bifida screening of spina bifida in serum

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