Mumps Virus IgM - India CDSCO Medical Device Registration

Mumps Virus IgM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001078_de39c5a8ba42aa95789ad5a28bc6b6b3_f0d49c7cf4b087dc46a3d42216fe30d3. 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

Mumps Virus IgM

UID: IMP/IVD/2020/001078_de39c5a8ba42aa95789ad5a28bc6b6b3_f0d49c7cf4b087dc46a3d42216fe30d3

Brand Name

NovaLisa®

License Holder

OSB Agencies Private Limiated

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Mumps VirusIgM ELISA is intended for the qualitative determination of IgM class antibodies against Mumps Virus in human serum or plasma (NovaLisa®)

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Parvovirus B19 IgM

Brand: NovaLisa®

OSB Agencies Private Limiated

Mumps Virus IgM - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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