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FT3 CLIA Test Reagent Kit - India CDSCO Medical Device Registration

FT3 CLIA Test Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000082_fd55d77d0a4be9ff80449e34a8625c24_85c5d3e33a5d933088e870d16560e80a. This device is marketed under the brand name BIOGENIX. The license holder is Biogenix Inc. Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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
FT3 CLIA Test Reagent Kit
UID: MFG/IVD/2020/000082_fd55d77d0a4be9ff80449e34a8625c24_85c5d3e33a5d933088e870d16560e80a

Brand Name

BIOGENIX

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

FT3 (BIOGENIX) Chemiluminescence immunoassay (BIOGENIX) kit is intended for the quantitative determination of FT3 (BIOGENIX) in human serum

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