EUROLAB laboratory provides testing and compliance services within the scope of ANSI AAMI IEC 60601-1-2 test standard. ANSI AAMI IEC 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.
The IEC 60601-1-2 standard covers general EMC requirements for basic safety and required performance for medical electrical devices and systems.
The purpose of the IEC 60601-1-2 standard is to specify general specifications and tests for electromagnetic compatibility (EMC) of medical electrical devices and systems.
Emission EMC Tests specified in the IEC 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.
EUROLAB assists manufacturers with ANSI AAMI IEC 60601-1-2 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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EUROLABreporting and certification activities, United Accreditation Foundation (UAF), Turkish Accreditation Agency (TÜRKAK) ve Enterprise Accreditation Foundation (EAF) based on the accreditation provided by the accreditation body. The Enterprise Accreditation Foundation (EAF) accreditation body is also a signatory of the United Nations (UN GLOBAL COMPACT) organization.
