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FT4 Rapid Quantitative Test - India CDSCO Medical Device Registration

FT4 Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000035_e3664b64baf174194ef86821c9a3cb98_9be6280aab63bde21ed61ae73b85c4bb. This device is marketed under the brand name Immunoglobulin E. 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
FT4 Rapid Quantitative Test
UID: IMP/IVD/2022/000035_e3664b64baf174194ef86821c9a3cb98_9be6280aab63bde21ed61ae73b85c4bb

Brand Name

Immunoglobulin E

License Holder

DIYA SCIENTIFIC

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Biotime FT4 Rapid Quantitative Test is intended to quantify the concentration of FT4 in human serum on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of hyperthyroidism. -Fluorescence immunoassay -hyperthyroidism For in vitro diagnostic use only. For professional use only.

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