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Medical
TUV Rheinland of North America, Inc. is your single source for all testing and certification needs. We perform conformity assessments to all European Medical Device Directives (MDD, IVDD, AIMDD) for CE Marking and are accredited by OSHA as a NRTL, as well as by the Standards Council of Canada, for testing and certification to a wide variety of standards. TUV Rheinland is an Accredited Person under the FDA 510(k) Third Party Review Program. The following list includes a brief summary of our services for the Medical Device In Vitro Diagnostic industries.