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TSH Fast Test Kit - India CDSCO Medical Device Registration

TSH Fast Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000153_d75a188daf0476470df138e9bcaca21a_9ff8635c7dd94c759ba87fb092f86c46. This device is marketed under the brand name Immunofluorescence Assay. The license holder is Cipla 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 Fast Test Kit
UID: IMP/IVD/2022/000153_d75a188daf0476470df138e9bcaca21a_9ff8635c7dd94c759ba87fb092f86c46

Brand Name

Immunofluorescence Assay

License Holder

Cipla Limited

Device Class

Class B

Approving Authority

CDSCO

Product Information

TSH Fast Test Kit (Immunofluorescence Assay) is intended for in vitro quantitative determination of thyroid-stimulating hormone (Immunofluorescence Assay) in serum and plasma. This test is used in the screening, clinical diagnosis, prognosis and therapeutic effect evaluation of thyroid diseases

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