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CMV IgG/IgM Antibody Rapid Test - India CDSCO Medical Device Registration

CMV IgG/IgM Antibody Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_dee4969a7311f24b4c2bef9cc1654ebe_829e3dab6602e0858a44e004f17c761a. This device is marketed under the brand name Chimera. The license holder is CHIMERA BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is South Delhi 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
CMV IgG/IgM Antibody Rapid Test
UID: MFG/IVD/2023/000113_dee4969a7311f24b4c2bef9cc1654ebe_829e3dab6602e0858a44e004f17c761a

Brand Name

Chimera

Device Class

Class B

Approving Authority

South Delhi Division

Product Information

The Chimeraยฎ CMV IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of the cytomegalovirus IgM/G antibody in serum /plasma. It is used as an aid in the diagnostic of past infection and epidemiological investigation

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