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CRP Test - India CDSCO Medical Device Registration

CRP Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000005_bcd9e8baa7fe12da9e51bf745645464a_0a58b615c5d272fcab6836910c1696b0. This device is marketed under the brand name Pathozyme® Ovarian Cancer Antigen Ag 125 ELISA. The license holder is Omega DX (Asia) Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO.

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 Test
UID: IMP/IVD/2018/000005_bcd9e8baa7fe12da9e51bf745645464a_0a58b615c5d272fcab6836910c1696b0

Brand Name

Pathozyme® Ovarian Cancer Antigen Ag 125 ELISA

Device Class

Class C

Approving Authority

CDSCO

Product Information

Avitex® CRP is an in-vitro diagnostic kit used for detection of C-Reactive Protein in human serum

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