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

Dengue IgG/IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000022_1b7c799a223f84d606c111737f26e671_c94d75859f9bc9ac48b7c0189bfabb5a. This device is marketed under the brand name Sensit. The license holder is Ubio Biotechnology Systems Private Limited, and it is classified as Device Class Class B. The approving authority is Kerala.

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 Rapid Test
UID: MFG/IVD/2020/000022_1b7c799a223f84d606c111737f26e671_c94d75859f9bc9ac48b7c0189bfabb5a

Brand Name

Sensit

Device Class

Class B

Approving Authority

Kerala

Product Information

Sensit Dengue IgG/IgM Test is an IVD medical device intended for the detection of Dengue IgG and IgM antibodies in human whole blood/ serum or plasma

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