Brucella IgG - India CDSCO Medical Device Registration

Brucella IgG is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001078_f68b05fa4cf244d3d1cec714e7cca962_9342553a2670bbae0de6f012936ef907. 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.

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CDSCO Registered

Class Class B

Brucella IgG

UID: IMP/IVD/2020/001078_f68b05fa4cf244d3d1cec714e7cca962_9342553a2670bbae0de6f012936ef907

Brand Name

NovaLisa®

License Holder

OSB Agencies Private Limiated

Device Class

Class B

Approving Authority

CDSCO

Product Information

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

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Brand: NovaLisa®

OSB Agencies Private Limiated

Brucella IgG - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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