Pure Global

C3 Fluid Pack - India CDSCO Medical Device Registration

C3 Fluid Pack is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000406_cfab783e2c5c0b81a1a02fcb49c249e9_4cbc73002ac15d60cbe6f3351e2c37cf. This device is marketed under the brand name C3 Fluid Pack. The license holder is Roche Diagnostics India 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
C3 Fluid Pack
UID: IMP/IVD/2019/000406_cfab783e2c5c0b81a1a02fcb49c249e9_4cbc73002ac15d60cbe6f3351e2c37cf

Brand Name

C3 Fluid Pack

Device Class

Class B

Approving Authority

CDSCO

Product Information

C3 Fluid pack for cobas b 121 system

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing