One step rapid test kit for differential detection of Chikungunya IgM & IgG Ab
- UID
- MFG/IVD/2020/000017_fbf3c3a389890566d27f2508a34dc507_e4ddabea46669b3e55afc686a3180019
- Device class
- Class B
- Brand name
- Standard F TSH FIA
- License holder
- SD Biosensor Healthcare Pvt. Ltd
- Approving authority
- Haryana
- Product information
- It is an immunochromatographic assay for the detection of IgM/IgG antibodies against Chikungunya virus in human serum, plasma or whole blood specimen
One step rapid test kit for differential detection of Chikungunya IgM & IgG Ab is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000017_fbf3c3a389890566d27f2508a34dc507_e4ddabea46669b3e55afc686a3180019. This device is marketed under the brand name Standard F TSH FIA. The license holder is SD Biosensor Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Haryana.
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.