The "Active Implantable Medical Devices
- Market Analysis, Trends, and Forecasts" report has been added to ResearchAndMarkets.com's offering.
* To address EMF concerns, we investigated the possibility that the human body and active implantable medical devices
were affected by the radiated emissions of WPT.
(3.) Council Directive 90/385/EEC on the approximation of the laws of Member States relating to active implantable medical devices
Variety of active implantable medical devices
(AIMD) malfunctions observed through electromagnetic fields (EMF) exposure Observed AIMD The source of EMF AIMD type * malfunctions exposure Pacing inhibition EAS systems [5,6]; CP (complete or induction hobs temporary stop of (25-34 kHz) ; pacing); the implant GSM [6,8-10]; interprets electrical vicinity of BTS potentials from EMF [11,12]; MD gates electrodynamic ; interaction as the MRI scanners (1.5 T) proper heart rate and [6,14]; ESU [6,15] stops the pacing, even in the absence of the intrinsic heart rate Triggering of rapid 2.1.
For Active Implantable Medical Devices
(AIMDs) like ReActiv8, CE Marking is granted by a Notified Body after review of the design dossier and other information for conformity to the AIMD Directive.
* 2020 Active implantable medical devices
reviewed for inclusion
Topics include the characteristics and applications of materials used for medical implants, precision machining, polyurethane in biomedical applications, customized cranio-facial implants design and manufacture, technological advances for polymers in active implantable medical devices
, integrated telemedicine systems, application of the finite method in spinal implant design and manufacture, and more.
The proposal on medical devices - which replaces Directives 90/385/EEC (active implantable medical devices
) and 93/42/EEC (medical devices) - clarifies the rights and responsibilities of the different stakeholders:- Manufacturers of medical devices (or their representative) will have to register with a European database and designate at least one qualified person in their organisation to monitor compliance with regulations.
In the UK, ALTs are regulated by the Medical Devices Directive ("MDD") and the Active Implantable Medical Devices
In the world of active implantable medical devices
, for example, every discarded unit can represent thousands of dollars in lost materials, labor, and revenue.
The two other medical devices Directives (Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices
and Council Directive 93/42/EEC concerning medical devices) were revised by Directive 2007/47/EC, and the need to revise Directive 98/79/EC was revealed by the public consultation that launched in 2008.
* The EC Active Implantable Medical Devices
Directive (European Commission 1990).