Erba Lisa® COVID-19 IgG - India CDSCO Medical Device Registration

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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CDSCO Registered

Class Class C

Erba Lisa® COVID-19 IgG

UID: MFG/IVD/2020/000014_d893dffb6efc23c916b4255eb0ea6d08_ca94bd3e6cf24f9d727d6f0c50878613

Brand Name

ERBAQIK Dengue Alpha NS1Ag

License Holder

M/s.Transasia Bio-Medicals Ltd.

Device Class

Class C

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.

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Erba Lisa® COVID-19 IgG

Brand: Erba Lisa

Transasia Diagnostics Private Limited

Erba Lisa® COVID-19 IgG - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

Erba Lisa® COVID-19 IgG

ERBAQIK Dengue IgG/IgM

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