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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/2022/000200_80a913c2fd3ddd4fadbbf7eeea463040_685f9a2713c042563f9cbc69e648ab79. This device is marketed under the brand name K+. The license holder is Siemens Healthcare Private Limited, 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
Urine Diluent
UID: IMP/IVD/2022/000200_80a913c2fd3ddd4fadbbf7eeea463040_685f9a2713c042563f9cbc69e648ab79

Brand Name

K+

Device Class

Class B

Approving Authority

CDSCO

Product Information

The ISE Module Urine Diluent is used for dilution of urine samples, for measuring the concentration of Li+, Na+, K+, and Cl- in diluted urine on clinical chemistry analyzers’ ISE Modules

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