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CDSCO UID MFG/IVD/2020/000014_d893dffb6efc23c916b4255eb0ea6d08_ca94bd3e6cf24f9d727d6f0c50878613

Erba Lisa® COVID-19 IgG

M/s.Transasia Bio-Medicals Ltd.Device Class Class CIndia CDSCOBrand: ERBAQIK Dengue Alpha NS1Ag
VerifiedCDSCO · official registry
Registration details
UID
MFG/IVD/2020/000014_d893dffb6efc23c916b4255eb0ea6d08_ca94bd3e6cf24f9d727d6f0c50878613
Device class
Class C
Brand name
ERBAQIK Dengue Alpha NS1Ag
Approving authority
Central Drug Standards Control Organization, West Zone
Product information
Coronavirus COVID-19 IgG antibody test Kit is intended for the qualitative detection of human anti–COVID 19 IgG antibody in human serum with coronavirus infection.
About this record

Erba Lisa® COVID-19 IgG is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000014_d893dffb6efc23c916b4255eb0ea6d08_ca94bd3e6cf24f9d727d6f0c50878613. This device is marketed under the brand name ERBAQIK Dengue Alpha NS1Ag. The license holder is M/s.Transasia Bio-Medicals 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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