October 6, 2021
Schlafender Hase Team
MDR e-Labeling
The EU Medical Device Regulations (MDR) states any device manufacturer with a website must publish user information in electronic form.
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MDR
October 6, 2021
Schlafender Hase Team
MDR Graphic Symbols
Over the last few posts, we have been touching upon different labelling requirements set by the MDR.
September 22, 2021
Schlafender Hase Team
MDR UDI and Device Registration
The new European Database on Medical Devices, known as EUDAMED, was originally scheduled to launch in May 2020,
