AMDR comments to the Spanish Royal Decree Regulating Medical Devices
The Association of Medical Device Reprocessors (AMDR) appreciates the opportunity to comment on [...]
Latvia: Changes in the legal landscape for medical devices in the Baltics – MDR/IVDR
As well as this, the draft regulations introduce the recycling and reuse of [...]
Legal Framework: Belgium
Belgium published guidelines for the remanufacturing of single use medical devices in January [...]
Legal Framework: Netherlands
The Netherlands published guidelines for the remanufacturing of single use medical devices in [...]
Legal Framework: Germany
The legal basis for reprocessing under German law (MP Betreiber V) changes on May 26 2021 [...]
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 [...]