These Instructions for Use and associated translations are provided in electronic format according to Commission implementing Regulation (EU) 2021/2226 of 14 December 2021 laying down rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as regards electronic instructions for use of medical devices.
Electronic versions are provided as PDF documents and a PDF reader is required to open the documents. PDF readers are commonly available at no cost for users. Refer to the applicable system and hardware requirements for the PDF reader that is used.
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