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Testosterone Assay (Testosterone Assay ) - India CDSCO Medical Device Registration

Testosterone Assay (Testosterone Assay ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000207_fcc8d7a3bdf1365e184a13bea61a7c17_6578baf26aefae4195c980f01e70010e. This device is marketed under the brand name CLIA. The license holder is Rapid House, 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 Assay (Testosterone Assay )
UID: IMP/IVD/2023/000207_fcc8d7a3bdf1365e184a13bea61a7c17_6578baf26aefae4195c980f01e70010e

Brand Name

CLIA

License Holder

Rapid House

Device Class

Class B

Approving Authority

CDSCO

Product Information

Testosterone Assay (CLIA) is for the in vitro quantitative determination of testosterone in human serum and plasma

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