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Urine Diluent - India CDSCO Medical Device Registration

Urine Diluent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000406_80a913c2fd3ddd4fadbbf7eeea463040_ff5cd359f91ffcb90204ba55d05c6c43. This device is marketed under the brand name cobas® 8000 data manager. The license holder is Roche Diagnostics India Pvt. Ltd., and it is classified as Device Class Class A. 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 A
Urine Diluent
UID: IMP/IVD/2019/000406_80a913c2fd3ddd4fadbbf7eeea463040_ff5cd359f91ffcb90204ba55d05c6c43

Brand Name

cobas® 8000 data manager

Device Class

Class A

Approving Authority

CDSCO

Product Information

The urine diluent is intended to be used for the dilution of urine prior to the measurement with 9180 Electrolyte Analyzer

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