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Brucella IgM ELISA - India CDSCO Medical Device Registration

Brucella IgM ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000101_a19ae45daf63efde40904ab852f1ee31_d1eedffe3297e924db9cee8da0369053. 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
Brucella IgM ELISA
UID: IMP/IVD/2021/000101_a19ae45daf63efde40904ab852f1ee31_d1eedffe3297e924db9cee8da0369053

Brand Name

NovaLisa

Device Class

Class B

Approving Authority

CDSCO

Product Information

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

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