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CK-MB - India CDSCO Medical Device Registration

CK-MB is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000191_8a863ab9781ae23a57fffc35f97a621d_05406df70f01a53599c86ff5e02de01e. This device is marketed under the brand name Testosterone Rapid Quantitative Test. The license holder is Matrix Labs, 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
CK-MB
UID: IMP/IVD/2019/000191_8a863ab9781ae23a57fffc35f97a621d_05406df70f01a53599c86ff5e02de01e

Brand Name

Testosterone Rapid Quantitative Test

License Holder

Matrix Labs

Device Class

Class B

Approving Authority

CDSCO

Product Information

Quantitative determination of CK-MB in human whole blood, serum or plasma.This test is used as an aid to assist in the diagnosis of acute myocardial infarction(Testosterone Rapid Quantitative Test)

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