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With the rapid advancement of technological advancements electronic medical equipment, the usage and production are rapidly changing. These products are becoming more popular and larger in scale. EN 60601-1-1:2010 describes a method that allows a manufacturer to examine, specify, create and test the usability. It relates to the safety requirements and essential specifications for the performance of medical electrical equipment. This usability engineering process evaluates and minimizes risks from issues with usability that are associated with the proper use. This standard should be kept in mind when you are involved with the manufacturing of medical equipment. See the top sist catalog standards sist-en-61058-2-5-1999 blog.

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