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FT-IgG/IgM Test - India CDSCO Medical Device Registration

FT-IgG/IgM Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000022_ef7231156963476be863092938a864d2_7afbe059d07a984b8dfa393a46dafb4b. 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
FT-IgG/IgM Test
UID: MFG/IVD/2020/000022_ef7231156963476be863092938a864d2_7afbe059d07a984b8dfa393a46dafb4b

Brand Name

Sensit

Device Class

Class B

Approving Authority

Kerala

Product Information

quickVET Feline Toxoplasma IgG/IgM Ab Test kit is an IVD medical device intended for the simultaneous and differential detection of Feline Toxoplasma IgG and IgM antibodies in Feline whole blood/serum/ plasma

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