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Mumps IgM ELISA - India CDSCO Medical Device Registration

Mumps IgM ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000040_ea7d4ff036982b01b5ae7ab324c9aaf3_29fc9d2886c1c9e8cc003bf646982ee0. This device is marketed under the brand name IL-6. The license holder is Krishgen Pudgala LLP, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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 IgM ELISA
UID: MFG/IVD/2022/000040_ea7d4ff036982b01b5ae7ab324c9aaf3_29fc9d2886c1c9e8cc003bf646982ee0

Brand Name

IL-6

License Holder

Krishgen Pudgala LLP

Device Class

Class B

Approving Authority

Kokan Division

Product Information

The Mumps IgM GENLISATM ELISA is intended for the qualitative determination of IgMclass antibodies in human serum and plasma

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