Australian Regulatory Guidelines for Medical Devices
Update: Notice to Stakeholders – Health Canada’s Regulatory Approach to Commercial Reprocessing of Medical Devices Originally Labelled for Single Use
EU National Rules on Reprocessing “Single-Use” Medical Devices Study on the implementation of Article 17 of Regulation (EU) 2017/745 on medical devices on the EU market
Healthcare Technologies Resource Guide
Regulations Relating to Medical Devices and In Vitro Diagnostic Medical Devices (IVDs)
UK Guidance on Remanufacturing
FDA SUD Reprocessing Regulation, 2000
FDA SUD Reprocessing Supplemental Regulation, 2002
