IEC 60601-2-26 Medical Electrical Equipment - Special Requirements for Basic Safety and Basic Performance of Electroencephalographs

Medical Device Tests

IEC 60601-2-26 Medical Electrical Equipment - Special Requirements for Basic Safety and Basic Performance of Electroencephalographs

The IEC 60601-2-26 standard applies to the basic safety and basic performance of electroencephalographs used in a clinical setting (eg hospital, doctor's office, etc.). This standard does not cover requirements for other equipment used in electroencephalography.

IEC 60601-2-26 Medical Electrical Equipment - Special Requirements for Basic Safety and Basic Performance of Electroencephalographs

This third edition cancels and replaces the second edition of IEC 60601-2-26. The purpose of this third edition is to bring this particular standard up to date with reference to the third edition of the general standard IEC 60601-1.

Special requirements for other equipment also used in electroencephalography are not within the scope of this standard, for example;

  • Cerebral function monitors;
  • Phonophotic stimulants;
  • Electroencephalographic telemetry;
  • EEG data storage and retrieval;
  • Equipment specifically for monitoring during electroconvulsive therapy;
  • Mobile electroencephalographic recordings.

EUROLAB assists manufacturers with IEC 60601-2-26 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.

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