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 MFG/IVD/2023/000103_a1f032c4ab0b7dcaa12fcfb337518520_dff1f7ee3d491993ac6d84c6fbb1cfd3. This device is marketed under the brand name RF-IgM. The license holder is Genovik Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Rajasthan.

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: MFG/IVD/2023/000103_a1f032c4ab0b7dcaa12fcfb337518520_dff1f7ee3d491993ac6d84c6fbb1cfd3

Brand Name

RF-IgM

License Holder

Genovik Biotech Pvt. Ltd.

Device Class

Class B

Approving Authority

Rajasthan

Product Information

Genovik Testosterone (RF-IgM) Test Kit is intended for the quantitative measurement of Total Testosterone (RF-IgM) in serum or plasma

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Brand: RF-IgM

Genovik Biotech Pvt. Ltd.

Testosterone Test - India CDSCO Medical Device Registration

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Device Class

Approving Authority

Product Information

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