MDD 93/42/EEC

The Medical Device Directive, Council Directive 93/42/EEC of 14 June 1993, harmonized the laws relating to medical devices within the European Union. Products conforming with the MD Directive must have a CE mark applied. The Directive was recently reviewed and amended by the 2007/47/EC and a number of changes were made. Compliance with the revised directive became mandatory on March 21, 2010. 
We manufacture Class I, IIa and IIb products according to the MDD product classification.