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TSH Test - India CDSCO Medical Device Registration

TSH Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_5acad52824337156d0d14901a0f15914_b58c86ef885e5c08ede9e4112ffe1900. This device is marketed under the brand name Finecare Beta-HCG Rapid Quantitative Test. The license holder is Star Biomed Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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 Test
UID: IMP/IVD/2021/000413_5acad52824337156d0d14901a0f15914_b58c86ef885e5c08ede9e4112ffe1900

Brand Name

Finecare Beta-HCG Rapid Quantitative Test

License Holder

Star Biomed Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Finecareโ„ข TSH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecareโ„ข FIA System (Finecare Beta-HCG Rapid Quantitative Test) for quantitative determination of thyroid stimulating hormone (Finecare Beta-HCG Rapid Quantitative Test) in human whole blood, serum or plasma

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