Diagnostic Kit for Serum Amyloid A
- UID
- IMP/IVD/2023/000169_0481b8c25a7a7932ae027dd654d7267e_22a1fb71ad7c5ac6bce8eab88f3da6ad
- Device class
- Class B
- Brand name
- Time-resolved Fluorescence Immunochromatographic Assay
- License holder
- Arkray Healthcare Pvt., Ltd.,
- Approving authority
- CDSCO
- Product information
- This test kit uses double antibody sandwich method principle and fluorescence immunochromatography analysis technology to quantitatively detect the concentration of SAA antigen in human serum, plasma, whole blood samples.
Diagnostic Kit for Serum Amyloid A is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000169_0481b8c25a7a7932ae027dd654d7267e_22a1fb71ad7c5ac6bce8eab88f3da6ad. This device is marketed under the brand name Time-resolved Fluorescence Immunochromatographic Assay. The license holder is Arkray Healthcare Pvt., Ltd.,, 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.