| Nombre | apoyo | Revisión | Disponibilidad | Fecha de emisión | Precio | ||
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PDF |
Inglés |
Vigente |
22/5/2017 |
441,00 € |
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Detalles
IEC TR 60601-4-1:2017(E) is intended to help a manufacturer through the key decisions and steps to be taken to perform a detailed risk management and usability engineering processes for medical electrical equipment or a medical electrical system, hereafter referred to as MEE or MES, employing a degree of autonomy (DOA).
This document provides a definition of DOA of MEE or MES and a medical robot, and also provides guidance on:
- methodologies to perform the risk management process and usability engineering for an MEE or MES with a DOA,
- considerations of basic safety and essential performance for an MEE and MES with a DOA, and
- identifying the use of DOA, and similar concepts in existing ISO/IEC standards dealing with MEE or MES with the goal to facilitate alignment of standards by consistent use of the concept of DOA, and
- distinguishing between medical robots, and other MEE and MES.
Unless specified otherwise, this document considers MEE and MES together.
The manufacturer of an MEE or MES with a DOA is expected to design and manufacture an MEE or MES that fulfils its intended use and does not have unacceptable risk throughout its life-cycle.
This document provides guidance to help the manufacturer in complying with the requirements of IEC 60601-1:2005 and IEC 60601-1:2005/AMD1:2012 for MEE and MES with DOA. The document is also intended as guidance for future standard writers.
There are no prerequisites to this document.
Información adicional
| Autor | International Electrotechnical Commission (IEC) |
|---|---|
| Comité | TC 62/SC 62A |
| Publicado por | IEC |
| Tipo de Documento | Norma |
| Edición | 1.0 |
| ICS | 11.040.01 : Equipo médico en general
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| Número de páginas | 80 |
| Palabra clave | IEC60601-4-1,IEC TR 60601-4-1:2017,IEC/TR 60601-4-1 |
| Formulario de pedido |
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