We provide importing services for worldwide medical device manufacturers in Europe and the United Kingdom compliant with the Medical Device Regulation (MDR) and In Vitro Device Regulation (IVDR)

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We provide non-EU medical and in-vitro device manufacturers with independent, hassle-free, European-wide importing services that are compliant with Medical Device Regulation (MDR) and In-Vitro Diagnostic Regulation (IVDR) requirements.

For non-EU medical device manufacturers working with GrowthImports means having one dedicated partner that ensures hassle-free MDR compliant importing of medical and IVD devices in Europe. Medical device importer will maintain flexibility, reduced risks and costs by having one independent import partner for all European healthcare markets.


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