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Dengue IgG/IgM - India CDSCO Medical Device Registration

Dengue IgG/IgM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_13f95ef30fdeba669c96f2a354f4c8a8_8687b1fd92f4904b368e444473321eb7. 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
Dengue IgG/IgM
UID: MFG/IVD/2023/000131_13f95ef30fdeba669c96f2a354f4c8a8_8687b1fd92f4904b368e444473321eb7

Brand Name

Rapid Widal

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Dengue IgG/IgM Combo is a lateral flow immunoassay for the simultaneous detection and differentition of IgG and IgM anti-dengue virus in human serum and plasma

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