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Direct Renin - India CDSCO Medical Device Registration

Direct Renin is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000339_f703fdd9b36296af504ce18707364964_2a38aad755e5c3b7c884032488373596. This device is marketed under the brand name CTX-I. The license holder is CPC DIAGNOSTICS PVT.LTD, and it is classified as Device Class Class B. 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 B
Direct Renin
UID: IMP/IVD/2022/000339_f703fdd9b36296af504ce18707364964_2a38aad755e5c3b7c884032488373596

Brand Name

CTX-I

Device Class

Class B

Approving Authority

CDSCO

Product Information

The IDS-iSYS Direct Renin assay is an in vitro diagnostic device intended for the quantitative determination of Direct Renin in human plasma on the IDS System

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