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Rheumatoid Factor IgM - India CDSCO Medical Device Registration

Rheumatoid Factor IgM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000251_f44fda19e10bd77e16962358502a0e82_6757f7f6b55aaf9e8111fc7d2fc30f8b. This device is marketed under the brand name NovaLisa®. The license holder is M/s Vishat Diagnostic 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
Rheumatoid Factor IgM
UID: IMP/IVD/2020/000251_f44fda19e10bd77e16962358502a0e82_6757f7f6b55aaf9e8111fc7d2fc30f8b

Brand Name

NovaLisa®

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Rheumatoid Factor IgM ELISA is intended for the quantitative determination of IgM rheumatoid factors in human serum or plasma (NovaLisa®)

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