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CRP LATEX KIT - India CDSCO Medical Device Registration

CRP LATEX KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000055_4bd2a973e0cefc1afa8a0fe143c031d4_46bbdfd5f1879a1e080940dd6e5904c4. This device is marketed under the brand name RAPHA SERO. The license holder is M/s Rapha Diagnostics PVt. Ltd.,, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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 C
CRP LATEX KIT
UID: MFG/IVD/2021/000055_4bd2a973e0cefc1afa8a0fe143c031d4_46bbdfd5f1879a1e080940dd6e5904c4

Brand Name

RAPHA SERO

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

Rapha Sero CRP latex REAGENT is a slide agglutination test for the qualitative and semi quantitative detection of C - reactive protein (RAPHA SERO) in human serum. Rapha Sero CRP latex is a slide agglutination test is for professional In Vitro diagnostic use only

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