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Coomb's Reagent - India CDSCO Medical Device Registration

Coomb's Reagent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000016_f512dd649be0bb93fbf49f58cc6493d6_c81b642035e1338b2ff22eba5b8fd0f7. The license holder is Genuine Biosystem Private Limited, and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South 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 D
Coomb's Reagent
UID: MFG/IVD/2019/000016_f512dd649be0bb93fbf49f58cc6493d6_c81b642035e1338b2ff22eba5b8fd0f7

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

A coomb's reagent is a medical device, intended for Anti Human Globulin serum with monoclonal Anti C

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