Select your location for location specific information:
The task of the Trade Supervisory Office at the Government of Upper Palatinate is to ensure safe products in the area of technical consumer protection. This includes active (energy-dependent) in-vitro diagnostics.
Economic operators (manufacturers, authorized representatives, importers and distributors) may only make safe in vitro diagnostic medical devices (IVDs) available on the market. They are responsible for ensuring that their products are designed in such a way that users and third parties are protected from risks to life and health. This is a significant contribution to the preventive protection of consumers and patients. The safety standard is based on EU legal requirements and European standards, which are decisive for the free movement of goods in the internal market. The European In Vitro Diagnostics Regulation (IVDR) is relevant for in-vitro diagnostics. The IVDR has been mandatory since May 26, 2022.
In order to ensure that only safe IVDs that meet the high European standards are placed on the market (i.e. reach the consumer / patient), the Bavarian Trade Inspectorate performs the following tasks in particular.
The trade supervisory authority
If you have any questions about the requirements for active in vitro diagnostic medical devices, or if you suspect that an active in vitro diagnostic medical device does not meet the prescribed requirements, you can contact the Trade Supervisory Office at the Government of the Upper Palatinate directly.
The task of the Trade Supervisory Office at the Government of Upper Palatinate is to ensure safe products in the area of technical consumer protection. This includes active medical devices (dependent on an energy source).
The Trade Supervisory Office at the Government of Swabia is responsible for monitoring environmentally friendly design (ecodesign) and energy consumption labeling.
Manufacturers, authorized representatives and importers (importers) of medical devices must register via the electronic system for the registration of economic operators (EUDAMED) before placing a product on the market.