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S3 Fluid Pack A - India CDSCO Medical Device Registration

S3 Fluid Pack A is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000406_3f2d262e5dd4dc54826f82477b017149_abdf03dcace66ec44913f63e27d3c26c. 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.

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CDSCO Registered
Class Class B
S3 Fluid Pack A
UID: IMP/IVD/2019/000406_3f2d262e5dd4dc54826f82477b017149_abdf03dcace66ec44913f63e27d3c26c

Brand Name

C3 Fluid Pack

Device Class

Class B

Approving Authority

CDSCO

Product Information

S3 Fluid pack A for cobas b 221 system

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