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TSH Rapid Quantitative Test - India CDSCO Medical Device Registration

TSH Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000035_2916948dd18deea876774be337549534_bc80ba3cdb40fd10186beeae8ca1f28c. The license holder is DIYA SCIENTIFIC, 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 Rapid Quantitative Test
UID: IMP/IVD/2022/000035_2916948dd18deea876774be337549534_bc80ba3cdb40fd10186beeae8ca1f28c

License Holder

DIYA SCIENTIFIC

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Biotime TSH ##PLACEHOLDER_0## Rapid Quantitative Test is intended to quantify the concentration of TSH in human serum or plasma on Biotime FIA Analyzers by fluorescent immunoassay. The test is used as an aid detection of hyperthyroidism or hypothyroidism

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