C-Reactive Protein Assay (C-Reactive Protein Assay )
- UID
- IMP/IVD/2020/000383_4b638ce6a30c66ffd3e804843adcfd0f_614f97b5d525d975abd1bdbd808dfab4
- Device class
- Class C
- Brand name
- Immunofluorescence
- License holder
- BIODX HEALTHCARE
- Approving authority
- CDSCO
- Product information
- The kit is used for the quantitative in vitro detection of C-Reactive Protein (Immunofluorescence) in human serum, plasma or whole blood samples
C-Reactive Protein Assay (C-Reactive Protein Assay ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000383_4b638ce6a30c66ffd3e804843adcfd0f_614f97b5d525d975abd1bdbd808dfab4. This device is marketed under the brand name Immunofluorescence. The license holder is BIODX HEALTHCARE, and it is classified as Device Class Class C. 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.