Active implantable medical devices(AIMDs) are complex products subject to rigorous regulatory standards by authorities across the globe. With both implantable and non‐implantable factors, as well as EMC and wireless considerations, manufacturers have a lengthy list of standards to know and to which they must comply. It is important to know which standards and requirements apply to a given product and to consider them throughout the production process to get a compliant, marketable product to the industry quickly and efficiently.
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