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HDL DIRECT TEST KIT - India CDSCO Medical Device Registration

HDL DIRECT TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000017_edefab203b944bdedf3a0fa3e2f644af_67b814e19f498be1f1442080ed406eb1. This device is marketed under the brand name SEROCON CYSTATIN C CONTROL SET. The license holder is Beacon Diagnostics Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Gujarat.

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
HDL DIRECT TEST KIT
UID: MFG/MD/2020/000017_edefab203b944bdedf3a0fa3e2f644af_67b814e19f498be1f1442080ed406eb1

Brand Name

SEROCON CYSTATIN C CONTROL SET

Device Class

Class B

Approving Authority

Gujarat

Product Information

quantitative determination of HDL cholesterol in serum/plasma

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