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Dengue IgG/IgM Rapid Test Kit - India CDSCO Medical Device Registration

Dengue IgG/IgM Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000069_cfd03df84801a562ed579ee3e69368e2_46e5a6124b08a0e3763c9f9cc83b1822. This device is marketed under the brand name LH. The license holder is PATHKITS HEALTHCARE PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Haryana.

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 IgG/IgM Rapid Test Kit
UID: MFG/IVD/2021/000069_cfd03df84801a562ed579ee3e69368e2_46e5a6124b08a0e3763c9f9cc83b1822

Brand Name

LH

Device Class

Class B

Approving Authority

Haryana

Product Information

It is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to dengue virus in human serum, plasma or whole blood

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