According to COMMISSION IMPLEMENTING REGULATION (EU) 2021/2226 of 14 December 2021, laying down implementing rules for Regulation (EU) 2017/745 of the European Parliament and of the Council as regards electronic instructions for use of medical devices, this page is intended exclusively for healthcare professionals.
By using this page, you confirm that you are a healthcare professional and accept the terms of use for this page.
Please note that the content of the instructions for use may vary depending on the regulatory requirements in your country.
According to Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002, and Regulation (EC) No 1223/2009, and repealing Council Directives 90/385/EEC and 93/42/EEC, eIFUs must be made available conventionally.
Paper versions of the IFU will be provided to you free of charge within 7 calendar days upon request.
To load, view, and print PDF files, you need appropriate software, such as Adobe Acrobat Reader. You can download the latest version of this program for free from the Adobe website (Adobe-Website herunterladen).
The Acrobat Reader can be accessed from your web browser if it is configured accordingly. If the PDF plugin is installed in your browser, PDF files will be displayed directly in the browser, allowing you to continue using your browser’s navigation features. If the plugin is not installed, the PDF file will be saved to your hard drive and opened with Acrobat Reader.