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Diagnostics test reagent kits for Ammonia - India CDSCO Medical Device Registration

Diagnostics test reagent kits for Ammonia is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000163_e38ad3b979293c03d7c0689dcd097cfc_e266b691b5e1157773b280ed30d800f0. The license holder is M/s Allied Biotechnology India Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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 B
Diagnostics test reagent kits for Ammonia
UID: MFG/IVD/2020/000163_e38ad3b979293c03d7c0689dcd097cfc_e266b691b5e1157773b280ed30d800f0

Device Class

Class B

Approving Authority

Kokan Division

Product Information

An Ammonia test reagent/ kit is a medical device intended for the estimation of Ammonia in serum/plasma/urine

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