European Commission’s Medical Device Sector, Reprocessing of Single-Use Devices Page
‘Reprocessing’ refers to a process carried out on a used device in order [...]
AMDR Response to Swedish MedTech Shadow Report
In December 2020, the Swedish National Board of Health and Welfare (Socialstyrelsen) released [...]
AMDR comments to the Slovenian Ministry of Health Proposal
The Association of Medical Device Reprocessors (AMDR) appreciates the opportunity to comment on [...]
AMDR Reaction to Swedish Socialstyrelsen Report: Prerequisites for Reprocessing and Reusing Disposable medical Devices in Sweden
The Association of Medical Device Reprocessors (AMDR) applauds the Swedish National Board of [...]
AMDR Comments to the European Commission’s Inception Impact Assessment on the Sustainable Products Initiative
The Association of Medical Device Reprocessors (AMDR) appreciates the Commission’s efforts to promote [...]
AMDR Comments to the European Commission’s Inception Impact Assessment on Empowering the Consumer for the Green Transition
The Association of Medical Device Reprocessors (AMDR) appreciates the Commission’s efforts to promote [...]
Commission Implementing Regulation (EU) 2020/1207; Single Use Devices
PDF Version: Commission Implementing Regulation (EU) 2020.1207 COMMISSION IMPLEMENTING REGULATION (EU) 2020/1207 [...]
United Nations Development Programme: Sustainable Health Procurement Guidance Note
To have an impact on planetary health requires bold vision, direction, leadership and [...]
AMDR filed comments to the European Commission’s Inception Impact Assessment on Waste Shipment Regulations
AMDR appreciates the Commission’s communication on a European Green Deal and efforts to [...]
Compliance Navigator BSI: Reuse of single-use medical devices in the European Union
Article 17 of the European Medical Devices Regulation 2017/745 (MDR) covers reprocessing of single-use [...]