EU Medical Device Regulation

EU #MDR (Medical Device Regulation) is the regulation of the European Union on the clinical investigation and sale of medical devices for human use and is effective as of 26 May 2021.

As Oruba Technology, we are dedicated to our partners, customers, and patients in Europe. We closely monitor regulatory developments and ensure strict compliance with quality standards for all our products and services.

And thanks to the EU – Turkey customs union for medical devices regulation, Turkey has the same regulations and rights as the EU countries.

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EU Medical Device Regulation

EU #MDR (Medical Device Regulation) is the regulation of the European Union on the clinical investigation and sale of medical devices for human use and is effective as of 26 May 2021.

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