The European Commission (EC) have recently published a draft implementing regulation regarding the safety and performance requirements for reprocessing single use devices, laying down rules for the application of Regulation (EU) 2017/745 as regards common specifications for the reprocessing of single-use medical devices.

Stakeholders are invited to provide comments on the document before 20th August 2019.

The Commission have a link on their website for stakeholders to provide feedback. For more information and to provide feedback to the EC directly, please visit the dedicated web page here.