If your company does not have a physical presence in Europe and you
wish to place a Medical Device or Invivo Diagnostic Device on the
market then European law stipulates that you must appoint an
Authorised Representative in Europe to liaise, for you, with the
Competent Authorities of the individual Member States.
Authorised Representative through PSF Medical ensures that you
meet the legal requirements for representation in Europe before
placing your medical device on the market. We can olso take care of
your Class 1 depositions.