Active Implantable Medical Devices
Given the surgical procedure involved and integration of a source of energy (electrical or not), such devices have to go through an intense amount of scrutiny to assure safety. ChallengesDevices covered by the Active Implantable Medical Devices (AIMD) rules are treated as Class III devices which require a thorough assessment procedure. AIMDs must meet the general requirements of harmonized standard EN 45502 as well as requirements to a specific family of device types. Not all Notified Bodies are recognized under directive 90/385/EEC (revised by the directive 2007/47/EC) to certify such devices. AdvantagesLNE/G-MED is recognized to assess Active Implantable Medical Devices and has significant experience certifying a wide range of devices for CE Marking, often in conjunction with ISO 13485, CMDCAS, third party FDA inspection and other certificates, to save the time and cost of multiple audits. You also benefit from:
Find Out MoreLNE/G-MED America offers in-person, online and other customized training on a wide range of certification and quality topics. For details, check out our training schedule or request a customized program.
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