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GAMMA GT TEST KIT - India CDSCO Medical Device Registration

GAMMA GT TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000121_5ea9e3d44bc08c5be27ea02d5002d4a9_5ee1401d37cb198e266843c305063eb9. This device is marketed under the brand name MyBio. The license holder is Beacon Diagnostics Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Gujarat.

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 TEST KIT
UID: MFG/IVD/2022/000121_5ea9e3d44bc08c5be27ea02d5002d4a9_5ee1401d37cb198e266843c305063eb9

Brand Name

MyBio

Device Class

Class B

Approving Authority

Gujarat

Product Information

Quantitative determination of Gamma GT in serum/plasma

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