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Hantavirus IgM ELISA - India CDSCO Medical Device Registration

Hantavirus IgM ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000101_80acc4824a8277f4aab74c101d7e3e5a_650ebb2f05b6f4f8af551fbf7ccadd9a. This device is marketed under the brand name NovaLisa. The license holder is Dia Sure Immunodiagnostic LLP, and it is classified as Device Class Class B. The approving authority is CDSCO.

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 B
Hantavirus IgM ELISA
UID: IMP/IVD/2021/000101_80acc4824a8277f4aab74c101d7e3e5a_650ebb2f05b6f4f8af551fbf7ccadd9a

Brand Name

NovaLisa

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Hantavirus IgM ELISA is intended for the qualitative determination of IgM antibodies against Hantavirus in human serum or plasma

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