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S2 Fluid Pack - India CDSCO Medical Device Registration

S2 Fluid Pack is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000406_73457712044479e923586617f7818ac0_a36e081348c5011c842b511d6f5fb873. 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
S2 Fluid Pack
UID: IMP/IVD/2019/000406_73457712044479e923586617f7818ac0_a36e081348c5011c842b511d6f5fb873

Brand Name

C3 Fluid Pack

Device Class

Class B

Approving Authority

CDSCO

Product Information

S2 Fluid pack for cobas b 221 system

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