TUV Rheinland provides medical device certification services to EN ISO 13485, EU Directives (MDR, IVDR) and the Medical Device Single Audit Program (MDSAP). TUV Rheinland is accredited by OSHA(US) / SCC(CA) as an NRTL, by the IECEE as a CBTL of CB Scheme, and by A2LA as part of the FDA ASCA program for the product safety testing of electrical and medical-electrical products. Additional services offered include RoHS/REACH, EMC/wireless/radio, Cybersecurity (incl. Penetration Testing & FDA 510(k) readiness services) and Market Access.