Pure Global

Myo - India CDSCO Medical Device Registration

Myo is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000039_9bd4075e113b7474ae358c76511d98e4_ca5a0784c997e5ed3d040341714635f0. This device is marketed under the brand name Finecare . The license holder is M/s Avantor Performance Materials India 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Myo
UID: IMP/IVD/2019/000039_9bd4075e113b7474ae358c76511d98e4_ca5a0784c997e5ed3d040341714635f0

Brand Name

Finecare

Device Class

Class B

Approving Authority

CDSCO

Product Information

"Quantitative determination of Myoglobin in human whole blood, serum or plasma. The test is used as an aid to assist in the diagnosis of acute myocardial infarction (Finecare ). "

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing