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Immunoglobulin E Rapid Test Kit(Insta Immunoglobulin E Rapid Test Kit) - India CDSCO Medical Device Registration

Immunoglobulin E Rapid Test Kit(Insta Immunoglobulin E Rapid Test Kit) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000130_dee15f127edc69edd27ba38ebb2b9b28_c199dd4a52b04ec98b11fb962c6496af. 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
Immunoglobulin E Rapid Test Kit(Insta Immunoglobulin E Rapid Test Kit)
UID: MFG/IVD/2022/000130_dee15f127edc69edd27ba38ebb2b9b28_c199dd4a52b04ec98b11fb962c6496af

Brand Name

Insta Chikungunya IgG/IgM Rapid Test

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

The Immunoglobulin E (Insta Chikungunya IgG/IgM Rapid Test) Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of Immunoglobulin E (Insta Chikungunya IgG/IgM Rapid Test) in human serum/plasma/whole blood specimens

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