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Reference Electrode - India CDSCO Medical Device Registration

Reference Electrode is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000200_960de3b40affeac3fb762b15afab0a87_a3487ea9de91a5fb2c5a7926926216a2. 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
Reference Electrode
UID: IMP/IVD/2022/000200_960de3b40affeac3fb762b15afab0a87_a3487ea9de91a5fb2c5a7926926216a2

Brand Name

K+

Device Class

Class B

Approving Authority

CDSCO

Product Information

The ISE Module Reference Electrode is used to measure the concentration of sodium, potassium, chloride and lithium in serum, plasma or diluted urine samples

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