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IEC 61936-1:2021 provides requirements for the design and the erection of electrical power installations in systems with nominal voltages exceeding 1 kV AC and nominal frequency up to and including 60 Hz, so as to provide safety and proper functioning for the use intended. This document does not apply to the design and erection of any of the following: – overhead and underground lines between…

L’IEC 61936-1:2021 fournit des exigences relatives à la conception et au montage des installations électriques dans des systèmes dont les tensions nominales sont supérieures à 1 kV en courant alternatif et la fréquence nominale inférieure ou égale à 60 Hz, afin d'assurer la sécurité et le fonctionnement correct pour l'utilisation prévue. L'installation électrique comprend…

This document specifies mechanisms for cross-domain password-based authenticated key exchange, all of which are four-party password-based authenticated key exchange (4PAKE) protocols. Such protocols let two communicating entities establish a shared session key using just the login passwords that they share with their respective domain authentication servers. The authentication servers, assumed to…

Le présent document spécifie les symboles utilisés pour exprimer les informations fournies pour un dispositif médical. Le présent document s’applique aux symboles utilisés pour une vaste gamme de dispositifs médicaux disponibles au niveau mondial et devant répondre à diverses exigences réglementaires. Ces symboles peuvent figurer sur le dispositif médical lui-même, sur son emballage ou dans les…

This document specifies symbols used to express information supplied for a medical device. This document is applicable to symbols used in a broad spectrum of medical devices, that are available globally and need to meet different regulatory requirements. These symbols can be used on the medical device itself, on its packaging or in the accompanying information. The requirements of this document…

Le présent document spécifie les exigences relatives aux informations à fournir par le fabricant du dispositif médical pour le traitement des dispositifs médicaux critiques ou semi-critiques (c’est-à-dire un dispositif médical qui pénètre dans des sites normalement stériles du corps humain ou un dispositif médical qui entre en contact avec des muqueuses ou une peau lésée) ou des dispositifs…

This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of critical or semi-critical medical devices (i.e. a medical device that enters normally sterile parts of the human body or a medical device that comes into contact with mucous membranes or non-intact skin) or medical devices that are intended to be sterilized. This…

This document establishes requirements and provides guidelines for “accessible tourism for all” with the aim of ensuring equal access and enjoyment of tourism by the widest range of people of all ages and abilities. This document provides information on the key aspects of policy making, strategy, infrastructure, products and services and is addressed to all stakeholders involved in the tourism…

This document specifies mechanisms for cross-domain password-based authenticated key exchange, all of which are four-party password-based authenticated key exchange (4PAKE) protocols. Such protocols let two communicating entities establish a shared session key using just the login passwords that they share with their respective domain authentication servers. The authentication servers, assumed to…

This document specifies the transformation of SysML (ISO/IEC 19514:2017) constructs to XSD (World Wide Web Consortium's XML schema definition language) constructs for the purpose of representing the SysML model represented in XMI (ISO/IEC 19509:2014) as XML (World Wide Web Consortium's XML) schemas. The specified mapping is a one-way transformation from SysML information model…