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Bordetella pertussis IgG - India CDSCO Medical Device Registration

Bordetella pertussis IgG is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001078_2a7258b1128e2d88495d2fa8d040ba95_f50fd48cdb2dfe3c287308655af108df. This device is marketed under the brand name NovaLisa®. The license holder is OSB Agencies Private Limiated, 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 IgG
UID: IMP/IVD/2020/001078_2a7258b1128e2d88495d2fa8d040ba95_f50fd48cdb2dfe3c287308655af108df

Brand Name

NovaLisa®

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Bordetella pertussis IgG ELISA is intended for the qualitative determination of IgG class antibodies against Bordetella pertussis in human serum or plasma (NovaLisa®).

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