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Emergency Room 13 Test Panel - India CDSCO Medical Device Registration

Emergency Room 13 Test Panel is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000494_d7bdfe5ea2400727c1fdd956b8960e2a_09300f5c7d2bd5395d6b19068ed21707. 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
Emergency Room 13 Test Panel
UID: IMP/IVD/2023/000494_d7bdfe5ea2400727c1fdd956b8960e2a_09300f5c7d2bd5395d6b19068ed21707

Brand Name

PushKang

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Emergency Room 13 Test Panel is intended for in vitro quantitative detection of the concentration or activity of Aspartate Aminotransferase (PushKang), Uric Acid (PushKang), Creatinine (PushKang), Glucose (PushKang), Creatine Kinase (PushKang), Creatine Kinase Isoenzyme (PushKang), Lactate Dehydrogenase (PushKang), ฮฑ-Hydroxybutyrate Dehydrogenase (PushKang), Amylase (PushKang), Potassium Ion (PushKang), Sodium Ion (PushKang), Chloride Ion (PushKang), Carbon Dioxide (PushKang) in human serum, plasma and whole blood by the microfluidic dry chemistry

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