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Dengue IgM ELISA Kit - India CDSCO Medical Device Registration

Dengue IgM ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000099_a0b475164f2063983eb59176bbbbe669_7b9daf489629264c980a6cd3593d27bb. This device is marketed under the brand name LDL. The license holder is Matrix Labs Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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
Dengue IgM ELISA Kit
UID: MFG/IVD/2021/000099_a0b475164f2063983eb59176bbbbe669_7b9daf489629264c980a6cd3593d27bb

Brand Name

LDL

License Holder

Matrix Labs Pvt Ltd

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

The Dengue IgM ELISA Test is an enzyme-linked immunosorbent assay designed for the qualitative detection of IgM antibodies against Dengue virus in human serum or plasma. The test kit is intended for professional use only

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