Rheumatoid Factor IgM Antibody TEST
- UID
- MFG/IVD/2023/000103_7d0589df2560bac1f0bd8f03eb40c86a_c16985b5d55e216c4c51326eb5f40a50
- Device class
- Class B
- Brand name
- RF-IgM
- License holder
- Genovik Biotech Pvt. Ltd.
- 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
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.
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