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EUROPEAN COMMISSION DG ENTERPRISEDirectorate G Unit 4 Pressure Equipment, Medical Devices, MetrologyMEDICAL DEVICES : Guidance documentMEDDEV 2.121 rev 4 April 2001GUIDELINES ON A MEDICAL DEVICES
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The European commission EC medical is a form required to be filed by companies seeking approval for medical products to be marketed in the European Union.
Manufacturers and distributors of medical products who wish to market their products in the European Union.
The form can be filled out online on the European Commission's official website by providing all necessary information about the medical product.
The purpose of the European Commission EC medical form is to ensure the safety and efficacy of medical products marketed in the European Union.
Information such as product details, manufacturing process, clinical trials data, and safety information must be reported on the European Commission EC medical form.
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