What is MDD?
The Medical Devices Directive (MDD) covers the mandatory regulatory requirements of the European Union for Medical Devices to fulfill CE certification requirements in order to export medical devices, of Class I, IIa, IIb, and III to any country within the European community. Compliance with the requirements of the Medical Devices Directive is declared by placing the CE Marking on the product, and supplying the device with a Declaration of Conformity.
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