Instruction to register the supply of alternative medical devices

A manufacturer, authorised representative, distributor, or importer can register the supply of an alternative medical device with the IGJ for medical equipment (class IIa/b and III) that do not carry a CE marking or that have not gone through the normal conformity assessment procedure.

An exception to this procedure is applicable for medical devices (like ventilators) and in-vitro diagnostics (tests) which are purchased via a central national working group initiated by the Ministry of VWS. Manufacturers and suppliers are requested to send specifications and information about the fulfilment of technical and clinical requirements to The inspection will forward the information to the relevant working group.

Registrations can be submitted by email to while referencing “Corona request care provider class II/III”.