EN 60601-1-2 standard is one of the Electromagnetic Compatibility (EMC) product family standards. Electrical medical product manufacturers design and have their products tested according to the EN 60601-1-2 standard.
EN 60601-1-2 standard covers general EMC requirements for basic safety and required performance for electrical medical devices and systems.
The purpose of the EN 60601-1-2 standard is to specify general specifications and tests for electromagnetic compatibility (EMC) of electrical medical devices and systems.
Emission EMC Tests specified in EN 60601-1-2 standard;
Immunity EMC Tests specified in EN 60601-1-2 standard;
Basic safety and required performance must be ensured for EMC Tests applied to electrical medical devices and systems. During or after the test; component failures, changes in programmable parameters, factory reset, change of operating mode, false alarms, noise or disturbance that may affect diagnosis, treatment and monitoring, etc. too many performance drops are not allowed.
Our EUROLAB laboratory test experts, with their professional working mission and principles, offer you, the manufacturer and suppliers, the best service and controlled testing process in our accredited laboratories within the scope of EN 60601-1-2 test standard.
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