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Renal Function Panel Test - India CDSCO Medical Device Registration

Renal Function Panel Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000494_18012bf7fa4c99302bf5e496c55c865f_d7a4a268417e712d2062dc5b285e8df5. 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
Renal Function Panel Test
UID: IMP/IVD/2023/000494_18012bf7fa4c99302bf5e496c55c865f_d7a4a268417e712d2062dc5b285e8df5

Brand Name

PushKang

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Renal Function Panel Test is intended for in vitro quantitative detection of the concentration of Albumin(PushKang), Uric Acid(PushKang), Creatinine(PushKang), UREA, Calcium Ion (PushKang), Carbon Dioxide(PushKang), and Inorganic Phosphorus (PushKang) in human serum, plasma and whole blood by the microfluidic dry chemistry

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