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Rheumatoid Factor IgM Antibody TEST - India CDSCO Medical Device Registration

Rheumatoid Factor IgM Antibody TEST is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000103_7d0589df2560bac1f0bd8f03eb40c86a_c16985b5d55e216c4c51326eb5f40a50. 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
Rheumatoid Factor IgM Antibody TEST
UID: MFG/IVD/2023/000103_7d0589df2560bac1f0bd8f03eb40c86a_c16985b5d55e216c4c51326eb5f40a50

Brand Name

RF-IgM

Device Class

Class B

Approving Authority

Rajasthan

Product Information

RF IgM is applicable to the quantitative detection of the concentration of IgM of Rheumatoid factor in human serum or plasma in vitro

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