Medical Devices
SZUTEST Konformitätsbewertungsstelle GmbH has applied to become a notified body within the framework of the Medical Device Regulation (EU) 2017/745.
WHAT SERVICES DOES SZUTEST OFFER FOR MEDICAL DEVICES?
The scope of the application includes MDR Medical Device Regulation (EU) 2017/745 in Annex IX Part I, Annex IX Part II and Annex XI Part A.
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![](https://www.szutest-germany.de/wp-content/uploads/2021/09/FR.MED_.166-Process-Flow-Chart-R02-1160x750.png)