Quality assurance

All products are developed and manufactured in accordance with the standard ISO 13485:2012, the current EU Medical Device Directive, the Canadian Medical Devices Regulation (CMDR), US 21 CFR 820 for the USA, and in accordance with a number of additional country-specific regulations.

MagPro transcranial magnetic stimulators and magnetic coils are approved as medical devices in Europe, the USA, Canada, China, Japan, South Korea, Australia, Russia, Brazil, and other markets worldwide.