Expert context
EU MDR listing checklist for B2B device offers
Legislation, clinical analyses and articles beside the catalogue. Some briefs sit behind Pro / Enterprise.
A CE-marked device listing on MedScope Exchange must name the legal manufacturer, the intended purpose, the class (as declared by the advertiser) and the regions where the offer may be published.
MedScopeGlobal does not act as a notified body. The advertiser remains responsible for the technical file and post-market surveillance.
Do not attach patient data, UDI traces tied to named individuals, or consumer-facing drug claims.