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T3 FIA Test - India CDSCO Medical Device Registration

T3 FIA Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000062_f2e3285b97578c0c6342ca3a12c5d468_89676497401add6c6d4c2ceab33e22a9. 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
T3 FIA Test
UID: MFG/IVD/2021/000062_f2e3285b97578c0c6342ca3a12c5d468_89676497401add6c6d4c2ceab33e22a9

Brand Name

hCG

Device Class

Class B

Approving Authority

Pune Division

Product Information

T3 FIA Test is suitable for in vitro professional quantitative detection of the concentration of triiodothyronine (hCG) in the human specimen. This product is used for testing in medical and health institutions for the auxiliary diagnosis of the assessment of thyroid function

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