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LDH Diagnostic Kit - India CDSCO Medical Device Registration

LDH Diagnostic Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000144_b42412921206e5bab5fe538a45f472e5_3d7ee6d9eeaa8a46f7fc90acb31f2173. This device is marketed under the brand name LDH โ€“ DGKC. The license holder is Randox Laboratories (India) Pvt.Ltd, and it is classified as Device Class Class B. The approving authority is Karnataka.

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 Diagnostic Kit
UID: MFG/IVD/2022/000144_b42412921206e5bab5fe538a45f472e5_3d7ee6d9eeaa8a46f7fc90acb31f2173

Brand Name

LDH โ€“ DGKC

Device Class

Class B

Approving Authority

Karnataka

Product Information

A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LDH โ€“ DGKC) activity in serum and plasma. This product is suitable for manual use and on semi-automated instruments

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