Safety and Performance Information

Clinically Relevant Solutions

Optimizing Patient Care

This page provides the Safety and Performance Information (SPI) of Nihon Kohden products as per the requirements defined in the

Section 23.1 of Annex I of the EU MDR: Medical Device Regulation 2017/745/EU.

This Safety and Performance Information is an extract from the General and Safety Information sections of the most recent edition of the

Operator’s Manual. For detailed operating procedures, follow the instructions of your Operator’s Manual.

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