CE Marking of Medical Devices According to 93/42/EEC Medical Devices Directive

CE marking of medical devices is a legal requirement to place a device on the market in the European Union. 93/42/EEC Directive lays out the safety and performance requirements for medical devices to be sold in the EU. The assessment criteria and requirements depend on the risk level, complexity of the device and its intended use.
NOTICE is appointed by the European Commission as Notified Body no 2764 for medical devices under the quality modules of the Medical Devices Directive, annexes II &V and has the expertise and experience to provide CE marking services.

Application Process

All that you need to do is to fill out our application form and provide us with the necessary and required information about your company and products.
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