Posts tagged medical device

European Commission amends EU RoHS to...

European Commission amends EU RoHS to add new Annex IV exemptions

December 14, 2021|Written by GreenSoft Technology, Inc. 3 New Exemptions Added To EU RoHS Annex IV List On November 15, the European Commission published an amendment to Annex IV of the EU RoHS Directive, which added 3 new phthalates exemptions. Annex IV lists exemptions which specifically apply to medical devices and monitoring and control instruments. […]

View our EU Medical Devices Regulatio...

View our EU Medical Devices Regulation (EU MDR) Educational Webinar

November 15, 2018 |Written by GreenSoft Technology, Inc. Now Available to View On-Demand: EU MDR Webinar On November 14, we hosted a webinar on the new EU Medical Devices Regulation (EU MDR). Hosted by Randy Flinders, this educational presentation covered: An overview of the EU Medical Devices Regulation (EU MDR) Your responsibilities and requirements as […]

Get Ready for the New EU Medical Devi...

Get Ready for the New EU Medical Devices Regulation

August 20, 2018 |Written by GreenSoft Technology, Inc. Compliance with New EU Medical Devices Regulation (EU MDR) Becomes Mandatory in May 2020 A new European regulation for medical devices is coming into effect in 2020. In May 2017, the EU Commission published the Medical Devices Regulation (MDR). The regulation becomes mandatory for medical device producers […]