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JEV IgM Rapid Test - India CDSCO Medical Device Registration

JEV IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000130_73dd15fe908ce39b0b6345684482121f_aaa7971496207d712b77b3df1e9c20ca. This device is marketed under the brand name Insta Chikungunya IgG/IgM Rapid Test. The license holder is Seloi Healthcare Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Greater Mumbai 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
JEV IgM Rapid Test
UID: MFG/IVD/2022/000130_73dd15fe908ce39b0b6345684482121f_aaa7971496207d712b77b3df1e9c20ca

Brand Name

Insta Chikungunya IgG/IgM Rapid Test

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

JEV Test is a rapid immunochromatography assay for the detection of IgM antibodies to JE virus in human whole blood, serum or plasma. The assay is used as a screening test for JEV infection and as an aid for diagnosis of infections in conjunction with other criteria

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