Mobile medical devices

Mobile medical devices

Red Overlay
Mobile medical devices
Mobile medical devices
Red Overlay

Unrivalled expertise from an EU Notified Body and UK Approved Body for mobile medical devices

As a manufacturer of software as a medical device, you must ensure that you meet the relevant regulatory requirements before placing your product onto the market; for the EU, these are outlined in the Medical Device Regulation (MDR) (EU) 2017/745 and, for the UK, the UK Medical Devices Regulations (UK MDR) 2002.






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