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Glucose and Lipid Panel Test - India CDSCO Medical Device Registration

Glucose and Lipid Panel Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000494_72a8a497d514a8f7a8980eab9fabe277_8caaab84311b3deabc3c23fda05a5ecc. 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
Glucose and Lipid Panel Test
UID: IMP/IVD/2023/000494_72a8a497d514a8f7a8980eab9fabe277_8caaab84311b3deabc3c23fda05a5ecc

Brand Name

PushKang

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Glucose and Lipid Panel Test is intended for in vitro quantitative detection of the concentration or activity of Glucose(PushKang), Triglyceride(PushKang), Total Cholesterol(PushKang), High Density Lipoprotein Cholesterol(PushKang), Glycated serum protein(PushKang) in human serum, plasma, and whole blood by the microfluidic colorimetry

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