Importers – The European Union Medical Device Regulation

If you are a non-EU manufacturer of medical devices or In-Vitro Diagnostic devices you need to comply with the Medical Device Regulation (MDR). The Regulation states manufacturers have to assign an importer that will have to meet the requirements and will be liable and responsible for placing products on the [url=https://www.growthimports.eu/article-13-mdrivdr]EU market[/url]. 

An Importer has different responsibilities from the other Economic Operators such as the Authorized Representative and Distributors. With GrowthImports you will comply with Article 13 and have an independent partner for your importing needs across Europe and the United Kingdom.

Import your medical goods Into Europe with our hassle-free market access Importing service while maintaining flexibility, compliance and Increased quality standards. With over 30 years of combined experience, GrowthImports is an ISO 13485 certified MDR/IVDR importer of record dedicated to ensure the facilitation of a compliant and smooth European wide importing into the European market.

Visit site https://www.growthimports.eu/article-13-mdrivdr