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cobas b 101 - India CDSCO Medical Device Registration

cobas b 101 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000476_db0ade96af474d93d8f8a6095f0520a2_ed6674c8a9fcd9b6059d00a8ba80c391. This device is marketed under the brand name cobas b 101. The license holder is Roche Diagnostics India Pvt. Ltd., 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
cobas b 101
UID: IMP/IVD/2023/000476_db0ade96af474d93d8f8a6095f0520a2_ed6674c8a9fcd9b6059d00a8ba80c391

Brand Name

cobas b 101

Device Class

Class C

Approving Authority

CDSCO

Product Information

The cobas b 101 system is intended for professional use in a clinical location setting or point-of-care (cobas b 101) locations.

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