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Myoglobin Detection Kit - India CDSCO Medical Device Registration

Myoglobin Detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000498_a64f88b0cde1b32d372d116660ee9d59_d4d3868dc7402d8c7ce084678975ade1. This device is marketed under the brand name Fluorescence Dry Quantitative Immunoassay. The license holder is Rivaara Labs Private Limited, 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
Myoglobin Detection Kit
UID: IMP/IVD/2021/000498_a64f88b0cde1b32d372d116660ee9d59_d4d3868dc7402d8c7ce084678975ade1

Brand Name

Fluorescence Dry Quantitative Immunoassay

Device Class

Class B

Approving Authority

CDSCO

Product Information

Quantitatively measuring the concentration of myoglobin (Fluorescence Dry Quantitative Immunoassay) in human serum/plasma/whole-blood.

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