Medical Device or Laboratory Equipment Evaluation
Ready to prove your production-equivalent device is compliant to the appropriate medical device or laboratory safety standards? A Medical Device or Laboratory Equipment Evaluation includes review of compliance to standards such as IEC 60601-1, IEC 61010-1, etc. including testing, documentation reviews, and report writing. The output of a medical device or laboratory equipment evaluation is a completed Test Report Form (TRF). Please see the Report Types page for details on the types of test reports MECA provides.