Are you looking for a specific OEM product? Please consider how Technomed Europe can serve your company! Together with our strategic partners we can develop your interconnect systems, needle and surface electrodes, sensors and a wide range of other medical accessories.

We can assist with your CE registration in Europe and/or act as your Authorized Representative in line with the regulations of the MDD/93/42/ECC directive.

Technomed Europe has instituted an effective quality assurance system. We work in a certified ISO 9001:2000 and ISO 13485:2003 environment compliant with the MDD/93/42/ECC directive. We are an FDA registered plant, work according to QSR standards and products developed by us can be FDA 510(k) registered.