Abstract
As a result of European unification, new regulations valid within the territory of
the European Union (EU) have been negotiated and published. As in other medical fields,
the Medical Device Directive (MDD) is the most important new regulation and also effects
endoscopy. In a transition period until June 1998, the MDD will be transposed into
national law by the member states of the EU. Compliance with the MDD and other European
regulations is indicated by the CE mark affixed to the product.
