Public Consultation on common specifications for products without an intended medical purpose under the MDR

The European Commission has opened a public consultation on a draft Implementing Regulation regarding common specifications for the group of products without an intended medical purpose, listed in Annex XVI of Regulation (EU) 2017/745 on medical devices (“MDR”).
The group of products concerned includes among others: cosmetic contact lenses, dermal fillers, aesthetic implants, equipment for body hair/tattoo removal (e.g. laser and intense pulsed light equipment), equipment for the destruction of adipose tissue (e.g. lipolysis, liposuction and lipoplasty equipment) as well equipment intended for brain stimulation.
The public consultation will remain open until 11 February 2022 (midnight Brussels time).
👉🏻 Public consultation:
👉🏻 Draft Implementing Regulation: