We are proud to announce that all Contract Medical International device CE certificates have been upgraded to the Annex II (Full Quality Assurance System) Conformity Assessment Procedure of the Council Directive 93/42/EEC by KEMA Quality notified body.

Annex II capability gives CMI the ability to act as its own ‘Notified Body’, and such as, has the most latitude allowed under the Medical Device Directive.

You can find all updated certificates here