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Gamma GT Reagent Test kit - India CDSCO Medical Device Registration

Gamma GT Reagent Test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000015_b87bc1ec5d2612500ac38834a8084c0d_04a538cc6ca4b425634d82f5995b4b1d. This device is marketed under the brand name 1:1. The license holder is DiaSys Diagnostics India Private Limited, 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
Gamma GT Reagent Test kit
UID: MFG/IVD/2022/000015_b87bc1ec5d2612500ac38834a8084c0d_04a538cc6ca4b425634d82f5995b4b1d

Brand Name

1:1

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Diagnostic reagent for quantitative in vitro determination of Gamma GT in human serum or heparin plasma or Urine on automated photometric systems

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