Safety of medical devices

The design of medical devices must consider the safety of users and third parties, as well as that of the patient. Medical devices often constitute work equipment and are therefore also an issue for occupational safety and health.

In the European Single Market, the nature of medical devices is governed by the EU Medical Devices Regulation (EU) 2017/745. The essential requirements set out in this European product regulation are intended to protect the safety and health of patients, users and third parties. The essential requirements can be supported in standards. KAN's work focuses on the safety and health of users of medical devices, in particular the following aspects:

Further information

  • KANBrief 1/22: Standardization of infection protection masks
  • KANBrief 4/21: Update on the safety of treatment tables
  • KANBrief 4/20: Treatment tables: safe raising and lowering
  • KANBrief 1/19: KAN expert discussion on the design of safe treatment tables

Do you have any questions on this topic, or need support? If so please contact Dr Anna Dammann.

News

Therapieliege © Frank Herrmann www.fh-photodesign.com-stock.adobe.com
2024-02-26

Third KAN expert discussion of the design of safe treatment tables

Following two fatal accidents on treatment tables, KAN organized…

Therapieliege © Frank Herrmann www.fh-photodesign.com-stock.adobe.com
2022-11-29

Update on the safety of treatment tables

On treatment tables with powered height adjustment, incidents in…

Eine Frau befindet sich unter einer Therapieliege. © BG BAU/Steindesign Werbeagentur
2021-03-16

New publication concerning treatment tables

In December 2020, the supreme regional authorities in Germany…

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