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Diagnostics test reagent kits for Gamma GT. - India CDSCO Medical Device Registration

Diagnostics test reagent kits for Gamma GT. is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000130_ed5fc6d90832257273754cd4c7993acd_a683e79484668b371a16f08ba55b04eb. The license holder is Vimek Bioconcept Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Greater Mumbai 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 Gamma GT.
UID: MFG/IVD/2021/000130_ed5fc6d90832257273754cd4c7993acd_a683e79484668b371a16f08ba55b04eb

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

A Gamma GT test reagent/ kit is a medical device intended for the estimation of Uric acid in serum/plasma

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