A whitepaper, How the Medical Device Regulation impacts the fluid and pneumatic systems used in medical technology, highlights some optimal approaches for integrating fluid and pneumatic components and systems into medical equipment, so that products can meet the strict requirements of the (EU) 2017/745 regulation, Medical Device Regulation (MDR).
There is a new requirement for medical device companies selling into the European market, called the Medical Device Regulation, or MDR. This new regulation places a focus on the supply chain, meaning suppliers in the industry must have a good understanding of the new...
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