The European Commission call for feedback on draft implementation regulation on Single-use medical devices.

News Category: Regulatory news

Date: 26/07/2019

The European Commission (EC) have recently published the safety and performance requirements for reprocessing single use devices under the new medical devices regulation. Stakeholders are invited to provide comments on the document before 20th August.

The HPRA and the Department of Health continue to work closely on developing our national position and encourage any stakeholder to contact us directly with feedback or queries by email to 

For more information and to provide feedback to the EC directly please visit the dedicated webpage below.  

Single-use medical devices - safety and performance requirements for reprocessing

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