From implants and instruments to single-use and combination products, as well as active electronic devices, Eurofins Medical Device Services offers the optimal testing strategy for all types of Class I, II, and III devices. We help verify product designs, confirm safety and efficacy, and ensure user needs are met.

With over 40 years of experience in preclinical testing and regulatory submissions, our scientists assist companies in navigating international regulatory requirements and scientific trends. Our 20+ state-of-the-art facilities across North America, Europe, and Asia Pacific provide a full scope of testing services, including Analytical Chemistry, Microbiology, Biocompatibility, Electrical & Mechanical, Packaging, Stability Testing, and Storage.

We are committed to global regulatory standards and quality systems compliant with cGMP, GLP, and ISO 17025, conducting tests in accordance with ISO, ASTM, ANSI, and AAMI standards to meet our customers' unique needs.