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CRP Turbidimetry Kit - India CDSCO Medical Device Registration

CRP Turbidimetry Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000005_e248a751a877499311ef542fa5fd98fa_272d9ad4f1ab406bfca4da649057f848. 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 Turbidimetry Kit
UID: IMP/IVD/2018/000005_e248a751a877499311ef542fa5fd98fa_272d9ad4f1ab406bfca4da649057f848

Brand Name

Pathozyme® Ovarian Cancer Antigen Ag 125 ELISA

Device Class

Class C

Approving Authority

CDSCO

Product Information

Avitex® Turbo CRP is a turbidimetry kit for measurement of C-Reactive Protein (Pathozyme® Ovarian Cancer Antigen Ag 125 ELISA) antibodies in human serum or plasma

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