CDSCO UID IMP/IVD/2020/000298_57ce9ce0b764ee7140ef0baaad24c4e5_d4409af969bcd15f3c0fab1102f361e1

Diagnostic Kit for IgM/IgG Antibody to Coronavirus

M/s GENES 2 ME PVT. LTD.·Device Class Class C·India CDSCO·Brand: SARS-CoV-2
Registration details
UID
IMP/IVD/2020/000298_57ce9ce0b764ee7140ef0baaad24c4e5_d4409af969bcd15f3c0fab1102f361e1
Device class
Class C
Brand name
SARS-CoV-2
Approving authority
CDSCO
Product information
This product is used for in vitro qualitative detection of Coronavirus (SARS-CoV-2) IgM/IgG antibody in human serum, plasma and venous whole blood samples. Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals. Results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status. Not for the screening of the general population. For professional use only.
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About this record

Diagnostic Kit for IgM/IgG Antibody to Coronavirus is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000298_57ce9ce0b764ee7140ef0baaad24c4e5_d4409af969bcd15f3c0fab1102f361e1. This device is marketed under the brand name SARS-CoV-2. The license holder is M/s GENES 2 ME PVT. LTD., and it is classified as Device Class Class C. The approving authority is CDSCO.

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