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LDH Kit(LDH-L ) - India CDSCO Medical Device Registration

LDH Kit(LDH-L ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_9faa1144a20ca0bafc025e93ba1290a5_6e7b65b816b5b7f2dc448634f9137479. This device is marketed under the brand name Rapid Widal. The license holder is BIOLAB DIAGNOSTICS (I) PVT. LTD., and it is classified as Device Class Class B. The approving authority is Kokan Division.

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 Kit(LDH-L )
UID: MFG/IVD/2023/000131_9faa1144a20ca0bafc025e93ba1290a5_6e7b65b816b5b7f2dc448634f9137479

Brand Name

Rapid Widal

Device Class

Class B

Approving Authority

Kokan Division

Product Information

It is used for estimation of LDH-L levels in human serum/plasma

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