Novel Coronavirus IgG/IgM Rapid Test kit
- UID
- IMP/IVD/2020/000170_f77d3e0fb85b1f22979815526a523c61_0ff0e6882fafec4159722f54af573f2c
- Device class
- Class C
- Brand name
- 2019-nCoV
- License holder
- Gland Pharma Limited
- Approving authority
- CDSCO
- Product information
- The product is a solid phase immunochromatographic assay for the rapid, qualitative/ semi-quantitative and differential detection of IgG and IgM antibodies to 2019-nCoV in human whole blood, serum or plasma
Novel Coronavirus IgG/IgM Rapid Test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000170_f77d3e0fb85b1f22979815526a523c61_0ff0e6882fafec4159722f54af573f2c. This device is marketed under the brand name 2019-nCoV. The license holder is Gland Pharma Limited, 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.