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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/2022/000074_aaa03697569fb48660cbaecced9585ba_0cf09ba21e18b99fd45587c82d61b534. This device is marketed under the brand name Glycated Hemoglobin. The license holder is FINOVA HEALTHCARE PRIVATE LIMITED, 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/2022/000074_aaa03697569fb48660cbaecced9585ba_0cf09ba21e18b99fd45587c82d61b534

Brand Name

Glycated Hemoglobin

Device Class

Class B

Approving Authority

CDSCO

Product Information

The TSH (Glycated Hemoglobin) Rapid Quantitative Test along with Aehealth FIA Meter is intended for vitro quantitative determination of Thyroid Stimulating Hormone (Glycated Hemoglobin) in human whole blood, serum or plasma. The test is used as an aid in the functional diagnosis of thyroidea

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