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Testosterone Test - India CDSCO Medical Device Registration

Testosterone Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000191_9240f2b36d673e1788512a88fbc5ea44_8b534cbdf248db9dc11516a56e710478. This device is marketed under the brand name Testosterone Rapid Quantitative Test. The license holder is Matrix Labs, 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
Testosterone Test
UID: IMP/IVD/2019/000191_9240f2b36d673e1788512a88fbc5ea44_8b534cbdf248db9dc11516a56e710478

Brand Name

Testosterone Rapid Quantitative Test

License Holder

Matrix Labs

Device Class

Class B

Approving Authority

CDSCO

Product Information

The FinecareTM Testosterone Rapid Quantitative Test is a fluorescence immunoassay used along with FinecareTM FIA Meters (Testosterone Rapid Quantitative Test) for quantitative measurement of Testosterone in human whole blood, serum or plasma. The test is to be used as an aid in the diagnosis of diseases related to abnormal testosterone levels

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