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medical device machining function selectionArticle Source： Tianyang Release Time：2018-09-21 Browse：
medical device machining function selection。As we all know, in the highly competitive medical device machining market, the majority of people are "medical device machining function selection" a strong interest. Tianyang Senior Editor From a professional point of view of milling knowledge level, let's give you a detailed description of medical device machining good service business's professional content.
The European version of the risk management standard was updated in 2009 and again in 2012 to refer to the Medical Devices Directive (MDD) and Active Implantable Medical Device Directive (AIMDD) revision in 2007, as well as the In Vitro Medical Device Directive (IVDD). The requirements of EN 14971:2012 are nearly identical to ISO 14971:2007. The differences include three "(informative)" Z Annexes that refer to the new MDD, AIMDD, and IVDD. These annexes indicate content deviations that include the requirement for risks to be reduced as far as possible, and the requirement that risks be mitigated by design and not by labeling on the medical device (i.e., labeling can no longer be used to mitigate risk).
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