Detection of Novel Coronavirus 2019-nCoV/SARS-CoV-2 from clinical samples
- UID
- MFG/IVD/2020/000021_1fe0f9146e20993c511915d88d374478_a6c646b4f839b02676d62698bfe2433b
- Device class
- Class C
- Brand name
- Multigene-Multiplex Single tube format
- License holder
- Mylab Discovery S0lutions Pvt. Ltd
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- Detection of 2019-Novel Coronavirus/SARS-CoV-2 in respiratory specimens and sera
Detection of Novel Coronavirus 2019-nCoV/SARS-CoV-2 from clinical samples is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000021_1fe0f9146e20993c511915d88d374478_a6c646b4f839b02676d62698bfe2433b. This device is marketed under the brand name Multigene-Multiplex Single tube format. The license holder is Mylab Discovery S0lutions Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.
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