The requirements of the Medical Device Regulation
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What do companies need to know specifically about the standard power supply of their medical device to ensure a smooth transition to the new regulations on May 26, 2021, and keep their products on the market?
The Medical Device Regulation (MDR) as a challenge for medical technology: What do manufacturers of medical devices need to know about their power supply?
The official application of the Medical Device Regulation was postponed by one year as a result of the Corona Pandemic. Manufacturers of medical devices thereby gain further valuable time to prepare for the implementation of the demanding directive.
But what do companies need to know specifically about the inconspicuous power supply of their application in order to make a clean transition to the new regulations on May 26, 2021 and to keep their approval on the market? And what should medical device manufacturers generally pay attention to when choosing their power supply?
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