EU Regulatory Resources

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 [...]

By |2020-11-18T14:32:18+00:00November 16th, 2020|EU Regulatory Resources|0 Comments

European Union, Medical Device Regulation of 2017, Regulation (EU) 2017/745 of the Euroepan Parliament and of the Council 5 April 2017, Article 17:

Single-Use Devices and their Reprocessing “…The reprocessing and further use of single-use devices [...]

By |2020-10-27T12:35:06+00:00May 5th, 2017|EU Regulatory Resources|0 Comments

Germany, Commission on Hospital Hygiene and Infection Prevention at the Robert Koch Institute and the Federal Institute for Drugs and Medical Devices (BfArM), Hygiene Requirements for the Reprocessing of Medical Devices (2012)

By |2020-10-27T12:36:25+00:00December 1st, 2012|EU Regulatory Resources|0 Comments