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LDH TEST KIT - India CDSCO Medical Device Registration

LDH TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000017_edbe64914f3c6bd65c3cc6cfbd35bd7e_3b17865c573aa38a1f266a85c0b10f85. 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
LDH TEST KIT
UID: MFG/MD/2020/000017_edbe64914f3c6bd65c3cc6cfbd35bd7e_3b17865c573aa38a1f266a85c0b10f85

Brand Name

SEROCON CYSTATIN C CONTROL SET

Device Class

Class B

Approving Authority

Gujarat

Product Information

Quantitative determination of LDH in serum/plasma

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