With the medical EMC and performance test, it is possible to ensure the electromagnetic compatibility of your medical devices to provide basic and necessary performance based on emissions and immune requirements.
In accordance with the medical EMC standard IEC 60601-1-2, medical devices are expected to perform and be safe for their intended use (basic performance and safety). IEC 60601-1-2 defines basic and fundamental performance for medical equipment in terms of emissions and immunity to electromagnetic disturbances.
IEC 60601-1-2 is valid for basic safety and basic performance in the presence of medical-electrical equipment and medical-electrical systems, electromagnetic disturbances as well as electromagnetic disturbances emitted by medical-electrical equipment and medical-electrical Systems.
IEC 60601-1-2 4th Edition introduced key technical revisions such as risk management, risk analysis and changes in immunity requirements. These key changes include determination of immunity testing levels based on intended use environments classified according to locations compliant with IEC 60601-1-11: professional healthcare facility environment, home healthcare environment, and special environments.
EUROLABis the first NRTL approved by OSHA for medical equipment. OSHA regulations cover all workplaces, including hospitals, clinics, therapy centers and similar facilities. EUROLAB Certified medical products are universally accepted in the United States and Canada.
EUROLAB Medical EMC testing by is typically performed according to EN/IEC 60601-1-2 for most devices. Additions and/or deviations from the requirements of 60601-2-60601 published in the appropriate EN/IEC 1-2-XX may also be applied for certain devices.
EUROLAB, with its highly expert team and internationally accredited laboratories, Medical EMC and Performance Tests It performs all test, analysis, measurement, evaluation and report generation services completely and reliably.
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