Testing End-to-End for Medical Safety
Service Detail from Eurofins E&E North America
End-to-end testing, certification, and evaluation helping you ensure the conformity of your Medical Electrical Equipment to product safety & essential performance requirements for global product approvals.
Product Safety requirements for electrical active medical devices are documented and internationally harmonized under the IEC 60601-xx standard family which is the base for the approval procedure of medical electrical equipment in most regulatory frameworks all over the world.
MET provides the full range of product safety testing per the 60601-1 series of standards including collateral (Part 1) and particular (Part 2) standards. In addition we offer complete testing for active implantable devices (ISO 14708).