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TSH FIA Test - India CDSCO Medical Device Registration

TSH FIA Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000062_c84d37e78c41d381219708ef19e1f956_3b0231612bd127f2779914d49fb5cd4a. This device is marketed under the brand name hCG. The license holder is Mylab Discovery Solutions Pvt. Ltd. Lonavla, and it is classified as Device Class Class B. The approving authority is Pune 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
TSH FIA Test
UID: MFG/IVD/2021/000062_c84d37e78c41d381219708ef19e1f956_3b0231612bd127f2779914d49fb5cd4a

Brand Name

hCG

Device Class

Class B

Approving Authority

Pune Division

Product Information

TSH FIA Test is an in-vitro diagnostic test used to measure TSH in human specimens. The quantity measurement of the TSH is useful in the diagnosis of hypothyroidism or hyperthyroidism. This test is only for professional use and it is used as an initial screening test

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