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Anti-Bordetella pertussis toxin ELISA - India CDSCO Medical Device Registration

Anti-Bordetella pertussis toxin ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000152_fb560baa3b8a4c3ddfded09f28438cb5_61c81339b62edda29373559f140b078f. This device is marketed under the brand name NIL. The license holder is M/s. CPC Diagnostics Pvt Ltd, 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
Anti-Bordetella pertussis toxin ELISA
UID: IMP/IVD/2022/000152_fb560baa3b8a4c3ddfded09f28438cb5_61c81339b62edda29373559f140b078f

Brand Name

NIL

Device Class

Class B

Approving Authority

CDSCO

Product Information

The ELISA test kit provides a quantitative in vitro assay for human antibodies of the immunoglobulin class IgG against Bordetella pertussis toxin in serum or plasma for the diagnosis of Bordetella pertussis infections and whooping cough

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