CMI complies with CAN/CSA ISO 13485
CMI has received CAN/CSA ISO 13485 certificate which is required by the Canadian medical device authorities from manufactures to be able to place their devices into the market in Canada. - Read more »
CMI has received CAN/CSA ISO 13485 certificate which is required by the Canadian medical device authorities from manufactures to be able to place their devices into the market in Canada. - Read more »
We are proud to announce that all Contract Medical International device CE certificates have been upgraded to the Annex II (Full Quality Assurance System) - Read more »
CMI is proud to be associated with the new medical device accelerator in Europe (MDA). - Read more »
We are proud to announce that both of our Dresden trainees successfully passed their exams this summer - Read more »
For a number of customers and applications, CMI has developed a kink resistant sheath material which has been used in cath - Read more »
Building on the commercially available Anson Refix™ System, a repositionable nitinol surgical clip, CMI and Lombard - Read more »
CMI worked together with researchers at the Leiden University Medical Center in The Netherlands under the direction of - Read more »