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CRP/MxA Antigen test - India CDSCO Medical Device Registration

CRP/MxA Antigen test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000130_c6e28063c15e39e690401d1d162cb375_59f8f9b82ff15dfda93e5d0967b4da12. 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
CRP/MxA Antigen test
UID: MFG/IVD/2022/000130_c6e28063c15e39e690401d1d162cb375_59f8f9b82ff15dfda93e5d0967b4da12

Brand Name

Insta Chikungunya IgG/IgM Rapid Test

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

The CRP/MxA combo test intended to assists diagnose viral & bacterial infections by measuring virus-specific markers and CRP simultaneously

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