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Myocardial Enzyme Panel Test - India CDSCO Medical Device Registration

Myocardial Enzyme Panel Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000494_f94187f6613a67fa47d1683dd56f8998_c81abd98cda954f9e0e628fa66bd2def. This device is marketed under the brand name PushKang. The license holder is Weldon Biotech India 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
Myocardial Enzyme Panel Test
UID: IMP/IVD/2023/000494_f94187f6613a67fa47d1683dd56f8998_c81abd98cda954f9e0e628fa66bd2def

Brand Name

PushKang

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Myocardial Enzyme Panel Test is intended for in vitro quantitative detection of the concentration or activity of Aspartate Aminotransferase (PushKang), Creatine Kinase (PushKang), Creatine Kinase Isoenzyme (PushKang), Lactate Dehydrogenase (PushKang), ฮฑ-Hydroxybutyrate Dehydrogenase (PushKang), in human serum, plasma and whole blood by the microfluidic dry chemistry

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