Safety and Performance Information

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.