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Dengue IgG/IgM Ab Test - India CDSCO Medical Device Registration

Dengue IgG/IgM Ab Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000145_12ee3a71825a27e1d5ffc0d5423f45e8_08fd9e799976a49c1f0e8a82580c47db. This device is marketed under the brand name SickleCatchโ„ข. The license holder is Mylab Discovery Solutions 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
Dengue IgG/IgM Ab Test
UID: MFG/IVD/2023/000145_12ee3a71825a27e1d5ffc0d5423f45e8_08fd9e799976a49c1f0e8a82580c47db

Brand Name

SickleCatchโ„ข

Device Class

Class B

Approving Authority

Kokan Division

Product Information

The Dengue IgG/IgM Ab test card is used for rapid visual tests for the qualitative detection of the presence or absence of Antibodies, specific to Dengue IgG/IgM antibody in human whole blood /Serum/Plasma specimens.

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