As of May 1, 2020, the European Union (EU) will be implementing changes to their current Medical Device Regulations aimed at overall device safety and effectiveness. Some changes that can be anticipated are device reclassification, as well as Safety and Performance Requirements.

In preparation for any possible impact to current contracts, HealthPRO is working diligently with suppliers to determine any anticipated changes or supply disruptions.

To best serve members, further information, including any impact and timelines, will be provided as soon as it is available.