Quality & Safety

The Magstim Company's aim is to provide biomedical devices of the highest quality of design and manufacture as well as safety, reliability and serviceability in use.

Magstim products comply with and are registered under the requirements of BS EN ISO 13485: 2003, Annexe II of the Medical Devices Directive, the FDA Good Manufacturing Practices: 21 CFR.820, and The Canadian Medical Devices Regulations.

They are also designed and built to numerous international safety standards, including BS-EN 60601-1, VDE 0750 and UL 544.