IEC TR 60601-4-1:2017
Norm
Medical electrical equipment - Part 4-1: Guidance and interpretation - Medical electrical equipment and medical electrical systems employing a degree of autonomy
- Gültig
Alle Preise inkl. MwSt.
Bleiben Sie mit der IEC-Watchlist immer auf dem neuesten Stand
Mit der IEC-Watchlist haben Sie die Möglichkeit, die für Sie relevanten Normnummern oder technische Fachgebiete in Ihre persönliche Watchlist aufzunehmen. Bei Erscheinen einer neuen IEC-Norm erhalten Sie automatisch eine E-Mail.
Um eine Norm der IEC-Watchlist hinzufügen zu können, müssen Sie sich zuerst einloggen.
Zuständiges Komitee:
Hauptnummer/Reihe:
60601
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.
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.
Dieses Dokument wird folgenden, in Fettschrift gekennzeichneten, Fachgebiet(en) zugeordnet:
- 11Medizintechnik
- 11.020Medizinische Wissenschaften im Allgemeinen. Gesundheitswesen im Allgemeinen
- 11.040Medizinische Geräte
- 11.060Zahnmedizin
- 11.080Sterilisation. Desinfektion
- 11.100Labormedizin
- 11.120Pharmazie
- 11.140Krankenhausausstattung
- 11.160Erstversorgung (Erste Hilfe)
- 11.180Hilfsmittel für Behinderte
- 11.200Geburtenkontrolle. Mechanische Verhütungsmittel
- 11.220Veterinärmedizin
Artikeldetails
- Edition: 1.0
- Umfang: 80 Seiten
- Sprache: Englisch
- Ausgabedatum: 2017-05
- Erscheinungsdatum: 2017-05-22
Item 1 of 9
Item 1 of 5






