The Office of Public Health is responsible for the market surveillance of medical devices and in-vitro diagnostic medical devices (IVD) in Liechtenstein. As part of this activity, it ensures that the medical devices and IVDs placed on the market, the procedures for placing them on the market and their handling comply with the legal requirements.

Notifications in the context of market surveillance

10. July 2023

The Office of Public Health requests Swiss authorized representatives (CH-REP) to review their mandates regarding ECM certifications. The following letter was sent to all CH-REPs registered with Swissmedic and based in Liechtenstein

Request to review mandates with regard to ECM certifications