Cover E DIN EN IEC 60601-2-33 VDE 0750-2-33:2022-09
larger

E DIN EN IEC 60601-2-33 VDE 0750-2-33:2022-09

Medical electrical equipment

Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

(IEC 62B/1247/CDV:2021); German and English version prEN IEC 60601-2-33:2021
Class/Status: Draft, valid
Released: 2022 -09   Published: 2022-08 -26
VDE Art. No.: 1701711
End of objection deadline: 2022-10-26

This document applies to the Basic Safety and Essential Performance of MR Equipment and MR Systems. NOTE Where ME Equipment and ME Systems are used in the clause headings, this is to be understood to indicate MR Equipment and MR Systems. This document does not cover the application of MR Equipment beyond the Intended use. If a clause or subclause is specifically intended to be applicable to MR Equipment only, or to MR Systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to MR Equipment and to MR Systems, as relevant. This document does not formulate additional specific requirements for MR Equipment or MR Systems used in Interventional MR Examinations.

Title Format
Entwicklung und Herstellung medizinischer Software
Prinz, Thorsten (Hrsg.)

Entwicklung und Herstellung medizinischer Software

Normen in der Medizintechnik
VDE-Schriftenreihe – Normen verständlich, Band 171

2017, 219 pages, Din A5, Broschur

Dieser Buchtitel ist auch als E-Book (PDF) erhältlich
Fachbuch eBook (PDF) Kombi-Fassung - Buch und E-Book