EU-MDR: what it means for our instruments and your registration

The EU Medical Device Regulation (EU-MDR, 2017/745) raised the bar for how medical devices are designed, documented and monitored across the European Union. For clinicians it means stronger safety and traceability; for distributors it means clearer, more complete technical documentation.

How we support you

For approved partners, we provide the documentation packs needed to register and place SG Manufacturers devices on your market. Visit our Quality & Certifications page or request access through the resource centre.