Início>FAQtos>FAQtos Técnicos>Limites de Exposição à Radiação Eletromagnética>Implants for surgery – Active implantable medical devices – Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
Título Implants for surgery – Active implantable medical devices – Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
Resumo This part 1 of EN 45502 specifies requirements that are generally applicable to active implantable medical devices. For particular types of active implantable medical devices, these essential requirements are supplemented or modified by the requirements of particular standards which form additional parts of this European Standard. The tests that are specified in EN 45502 are type tests and are to be carried out on samples of a device to show compliance. This part of EN 45502 is applicable not only to active implantable medical devices that are electrically powered but also to those powered by other energy sources (for example by gas pressure or by springs). This part of EN 45502 is also applicable to some non-implantable parts and accessories of the devices. The device that is commonly referred to as an active implantable medical device may in fact be a single device, a combination of devices, or a combination of a device or devices and one or more accessories. Not all of these parts are required to be either partially or totally implantable, but there is a need to specify some requirements of non-implantable parts and accessories if they could affect the safety or performance of the implantable device. The terminology used in this European Standard is intended to be consistent with the terminology of Directive 90/385/EEC.
Fonte European Committee for Electrotechnical Standardization (CENELEC)
Origem Internacional
Autor/Editor IEC Sub-Committee 62D
Disponibilidade Disponível por encomenda
Link cenelec.eu
Referência EN 45502-1:2015
Data Maio 2015
2020-02-10T10:37:59+00:00
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