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Bordetella pertussis IgM ELISA - India CDSCO Medical Device Registration

Bordetella pertussis IgM ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000101_827921f6ef5db419f9b86484b4c34a41_385ff55712e8135bceb2c937b8e4968c. 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
Bordetella pertussis IgM ELISA
UID: IMP/IVD/2021/000101_827921f6ef5db419f9b86484b4c34a41_385ff55712e8135bceb2c937b8e4968c

Brand Name

NovaLisa

Device Class

Class B

Approving Authority

CDSCO

Product Information

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

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