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Dengue Antibody Test (Dengue Antibody Test ) - India CDSCO Medical Device Registration

Dengue Antibody Test (Dengue Antibody Test ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000079_821b3686dc31b596d1d2a9a7a9dddfad_b7b450fa1175c2e0cc150e9b8f62ce82. This device is marketed under the brand name IgM/IgG. The license holder is Oscar Medicare Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttarakhand.

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 Antibody Test (Dengue Antibody Test )
UID: MFG/IVD/2021/000079_821b3686dc31b596d1d2a9a7a9dddfad_b7b450fa1175c2e0cc150e9b8f62ce82

Brand Name

IgM/IgG

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

DENGUE ANTIBODY TEST (IgM/IgG) is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of dengue specific antibody (IgM/IgG) in human serum / plasma for diagnosis of dengue infection. For professional use only

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