Europlaz Technologies Ltd

Europlaz Technologies Ltd

The Maltings Industrial Estate, Southminster CM0 7EQ

CE Marking Medical Devices

CE Marking Medical Devices

Class I or IIa Medical Device CE Mark Applications on Your Behalf

As part of the overall ‘concept to completion’ service, Europlaz can support the Regulatory CE Marking processes for medical devices. Services range from individual Technical File elements such as testing and production documentation to managing the complete CE Marking process, including the generation and ongoing maintenance of the Technical File.

In order to apply a CE Mark to a medical device, it is necessary to demonstrate the device meets the requirements in the appropriate Medical Device Directive / Medical Device Regulation by following the relevant, comprehensive conformity assessment procedures.

Product Enquiry

SSL Secure Connection