As of May 26, 2021, Switzerland is considered a third country beside the EU. The mutual recognition of conformity assessment procedures no longer applies. As a result, foreign manufacturers of medical devices must appoint a "Swiss Authorised Representative".
For manufacturers from outside Switzerland, we are available for designation as Swiss Authorised Representative.
As of May 26, 2021, Switzerland is considered a third country beside the EU. The mutual recognition of conformity assessment procedures no longer applies. As a result, foreign manufacturers of medical devices must appoint a "Swiss Authorised Representative".
For manufacturers from outside Switzerland, we are available for designation as Swiss Authorised Representative.
Swiss importers and distributors of in vitro diagnostic medical devices must comply with their obligations under (EU) 2017/746 IVDR.
We support your company in a competent and uncomplicated way.
Swiss importers and distributors of in vitro diagnostic medical devices must comply with their obligations under (EU) 2017/746 IVDR.
We support your company in a competent and uncomplicated way.
