Date & Time
Dec 3, 2020 10:00am CET
Webinar will be held in Polish.
Any changes to a standard can create concern for medical device manufacturers regarding the effects it will have on their products and compliance.
In this session we will discuss the changes that resulted with Amendment 2, of the IEC 60601-1 standard, to allow you to start thinking about the impact on your products. We will cover the base standard, high level changes and the potential effects it will have on your operation.
Engineer Project Associate
UL International Polska Sp. z o.o.