COVID-19 Neutralizing Antibody ELISA Test - India CDSCO Medical Device Registration

COVID-19 Neutralizing Antibody ELISA Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000029_e9850d71276ebb666bbd46a356eed0a0_3ec22b4d34ba9eb25d2fdefa250de89c. This device is marketed under the brand name Merilisa. The license holder is Meril Diagnostics Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered

Class Class C

COVID-19 Neutralizing Antibody ELISA Test

UID: MFG/MD/2018/000029_e9850d71276ebb666bbd46a356eed0a0_3ec22b4d34ba9eb25d2fdefa250de89c

Brand Name

Merilisa

License Holder

Meril Diagnostics Pvt. Ltd.

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Covid - 19 Neutralizing Antibody Detection Kit is a blocking enzyme-linked immunosorbent assay intended for qualitative direct detection of total neutralizing antibodies to covid-19 in human serum and plasma

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Drug of Abuse Rapid Test- MDMA-500mg/ml

Brand: Merilisa

Meril Diagnostics Pvt. Ltd.

COVID-19 Neutralizing Antibody ELISA Test - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

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