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/2021/000116_d893dffb6efc23c916b4255eb0ea6d08_a48fc9778446781fab80f8231b1862a6. This device is marketed under the brand name Erba Lisa. The license holder is Transasia Diagnostics Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO, Zonal office, Hyderabad.

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CDSCO Registered

Class Class C

Erba Lisa® COVID-19 IgG

UID: MFG/IVD/2021/000116_d893dffb6efc23c916b4255eb0ea6d08_a48fc9778446781fab80f8231b1862a6

Brand Name

Erba Lisa

License Holder

Transasia Diagnostics Private Limited

Device Class

Class C

Approving Authority

CDSCO, Zonal office, Hyderabad

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

Class C

Brand: Erba Lisa

Class C