CEN /TC10 EN81-20:2014(E) CEN /TC10 Secretariat :AFNOR Safety rules for the construction and installation of lifts Lifts for the transport of persons and goods - Part20 :Passenger and goods passenger lifts Sicherheitsregeln fur die Konstruktion und den Einbau von Aufzugen Aufzuge fur den Personen -und Gutertransport-Teil 20 :Personen -und Lastenaufzuge Regles de securite pour la construction et l'installation des elevateurs Elevateurs pour le transport de personnes et d'objets - Partie20 : Ascenseurs et ascenseurs de charge ICS : Descriptors : en81-20:2014(e) Contents Foreword .. Introduction 0.1 General ... 0.2 General remarks 0.3 Principles 0.4 Assumptions 1 Scope 2 Normative references 3 Terms and definitions 4 List significant hazards Safety requirements and /orprotective measures 5.1 General .... 5.2 Well ,machinery spaces and pulley rooms 5.2.1 General provisions 5.2.2 Access to well and to machinery spaces and pulley rooms 5.2.3 Access and emergency doors Access trap doors Inspection doors . 5.2.4 Notices 5.2.5 Well . 5.2.6 Machinery spaces and pulley rooms 5.3 Landing doors and car doors 5.3.1 General provisions 5.3.2 Height and width of entrance...
EUROPEAN STANDARD ENISO 7198 NORME EUROPEENNE EUROPAISCHE NORM March 2017 ics11.040.40 Supersedes EN 12006-2 :1998 +A1:2009 English Version Cardiovascular implants and extracorporeal systems Vascular prostheses Tubular vascular grafts and vascular patches ( 7198 :2016 ) Implants cardiovasculaires et systemes extracorporels Kardiovaskulare Implantate und extrakorporale Protheses vasculaires -Greffons vasculaires Systeme -Vaskulare Prothesen-Tubulare vaskulare tubulaires et pieces vasculaires ( 7198 :2016 ) Transplantate und GefaBpatches ( 7198 :2016 ) This European Standard was approved by CEN on 8 July 2016 . CEN members are bound to ply with the CEN /CENELECInternal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration .Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member . This European Standard exists in three official versions ( English,French ,German ).A version in any other language made by translation under the responsibility of a CEN member into its own langu...
s .[ o ] :osi pue ][dxajo ozoz .+oI-g' aouaps ap an : .3373N33-N30 ? : . :OSI sapas . 090s8s ZOZ .Ien. awdo 9ES OSI NG aaVaNVLS :9EsNa sa BS EN ISO 536 :2020 EN ISO 536:2020e) European foreword This document ( ENISO 536 :2020 )has been prepared by Technical Committee ISO /TC"Paper,board and pulps "in collaboration with Technical Committee CEN /TC172 " Pulp,paper and board "the secretariat of which is held by DIN . This European Standard shall be given the status of a national standard ,either by publication an identical text or by endorsement ,at the latest by August 2020 ,and conflicting national standards shall be withdrawn at the latest by August 2020 . Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights .CEN shall not be held responsible for identifying any or all such patent rights . This document supersedes EN ISO 536 :2012 . According to the CEN-CENELEC Internal Regulations ,the national standards organizations of the following countries are bound to implement this European Standard :Austria ,Belgium ,Bulgaria , Croatia ,Cyprus ,Czech Republic ,Denmark ,Estonia ,Finland ,France ,Germany ,Greece ,...
EUROPEAN STANDARD EN ISO 15223-1 NORME EUROPEENNE EUROPAISCHE NORM September 2021 01.080.2011.040.01 Supersedes EN ISO 15223-1 :2016 English Version Medical devices Symbols to be used with information to be supplied by the manufacturer Part 1 :General requirements ( 15223-1 :2021 ) Dispositifs medicaux Symboles a utiliser avec Medizinprodukte -Zu verwendende Symbole informations a fournir par le fabricant -Partie mit durch den Hersteller bereitgestellten 1 :Exigences generales ( 15223-1 :2021 ) Informationen Teil 1 :Allgemeine Anforderungen ( 15223-1 :2021 ) This European Standard was approved by CEN on 4 June 2021 . CEN and CENELEC members are bound to ply with the CEN /CENELECInternal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration .Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN and CENELEC member . This European Standard exists in three official versions ( English,French ,German ).A version in any other language made by translation under the responsibility o...
EUROPEAN STANDARD EN ISO 14971 NORME EUROPEENNE EUROPAISCHE NORM December 2019 ICS11.040.01 Supersedes EN ISO 14971 :2012 English version Medical devices - Applicationof risk management to medical devices ( 14971 :2019 ) Dispositifs medicaux -Application de la gestion des Medizinprodukte -Anwendung des risques aux dispositifs medicaux ( 14971 :2019 ) Risikomanagements auf Medizinprodukte ( ISO 14971:2019 This European Standard was approved by CEN on 5 August 2019 . CEN and CENELEC members are bound to ply with the CEN /CENELECInternal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration .Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN and CENELEC member . This European Standard exists in three official versions ( English,French ,German ).A version in any other language made by translation under the responsibility of a CEN and CENELEC member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official versions . CEN and CENE...
EUROPEAN STANDARD EN ISO 10993-1 NORME EUROPEENNE EUROPAISCHE NORM December 2020 is11.100.20 Supersedes EN ISO 10993-1 :2009 English Version Biological evaluation of medical devices Part 1 Evaluation and testing within a risk management process ( ISO10993-1 :2018 ,including corrected version 2018-11 ) Evaluation biologique des dispositifs medicaux Partie Biologische Beurteilung von Medizinprodukten Teil 1 : 1 :Evaluation et essais au sein d'un processus de Beurteilung und Prufungen im Rahmen eines gestion du risque ( 10993-1 :2018 ,y pris Risikomanagementsystems ( 10993-1 :2018 , version corrigee 2018-11 ) einschlieBlich korrigierte Fassung 2018-11 ) This European Standard was approved by CEN on 10 December 2020 . CEN members are bound to ply with the CEN /CENELECInternal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration .Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member . This European Standard exists in three official versions ( English,French ,German ).A ...
DS Dansk standard ds/en746-2 2 .udgave 2010-06-01 Udstyr til industrielle termiske procesanlaeg Del 2 :Sikkerhedskrav 568668 til fyrings-og braendstofsystemer Industrial thermoprocessing equipment -Safety requirements for bustion and fuel handling systems DANSK STANDARD Danish Standards Kollegievej 6 DK-2920 Charlottenlund el:+4539966101 Fax+4539966102 dansk standard @ds.dk .ds.dk Dansk Standard Eftertryk uden tilladelse forbudt ds/en746-2 Kobenhavn DS projekt :M212672 ics:25.180.01 Forste del af denne publikations betegnelse er DS /EN,hvilket betyder ,at det er en europaeisk standard ,der har status som dansk standard . Denne publikations overensstemmelse er : IDT med :en746-22010. DS-publikationen er pa engelsk . Denne publikation erstatter :DS /EN746-2 :1997 . DS-publikationstyper Dansk Standard udgiver forskellige publikationstyper . Typen pa denne publikation fremgar af forsiden . Der kan vaere tale om : Dansk standard standard ,der er udarbejdet pa nationalt niveau ,eller som er baseret pa et andet lands nationale standard ,eller standard ,der er udarbejdet pa internationalt og /ellereuropaeisk niveau ,og som har faet status som dansk standard DS-i...
EUROPEAN STANDARD EN62366 NORME EUROPEENNE EUROPAISCHE NORM April 2015 ics11.040 English Version Medical devices -Part 1 :Application of usability engineering to medical devices (eC62366-1:2015) Dispositifs medicaux -Partie 1 :Application de lingenierie Medizinprodukte Anwendung der Gebrauchstauglichkeit de l'aptitude a I'utilisation aux dispositifs medicaux auf Medizinprodukte (ec62366-1:2015) (ec62366-1:2015) This European Standard was approved by CENELEC on 2015-03-31 .CENELEC members are bound to ply with the CEN /CENELEC Intemal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration Up-to-date lists and bibliographical references such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CENELEC member . This European Standard exists in three official versions ( English,French ,German ).A version any other language made by translation under the responsibility of a CENELEC member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official versions CENELEC members are the national electrotechn...
建筑 形式与功能 之间的矛盾 The Contradiction Between Form and Function i Architecture 美]约翰香农亨德里克斯(John Shannon Hendrix ) 吴梦译 机械工业出版社 CHINA MACHINE PRESS 建筑形式与 功能之间的矛盾 The Contradiction Between Form and Function in Architecture [美]约翰·香农·亨德里克斯 ( JohnShannon Hendrix ) 吴梦译 机械工业出版社 本书论述了形式与功能的矛盾性在建筑创作策略中的重要性。在建筑学中,建筑形式 与功能的矛盾性被认为是建筑诗意的表现手法以及表达建筑理念的一种手段。 本书迪过对建筑史及建筑理论的研究分析,从维特鲁威(Vitruvius )时代到现在,尤 其重点研究了20世纪功能主义,得出了形式与功能矛盾性的重要性。书中列举了众多历 史案例,从远古建筑、古典建筑、伊斯兰建筑拜占庭建筑、哥特式建筑到文艺复兴、风 格主义和新古典主义建筑,乃至20世纪至今的运动思潮。除此之外,书中还探讨了历史 上与建筑创作相关联的哲学问题,如特征、表象、延异、梦的构成、深层结构与表层结 构,拓扑理论、自我实现和内在性等 本书有助于将建筑学作为一门人文学科重新对待,强调建筑在理念表达上的作用,以 及人类智慧中建筑作为伦理角色的参与,从而让建筑成为表达人类同一性的一种方式。 Copyright 2013 by Routledge Authorized translation from English language edition published by Routledge ,part of Taylor Francis Group LLC :All rights ;本书原版由&Francis 出版集团旗下,Routledge 出版公司出版,并经其授权翻译出版,版权所有,侵权必究 China Machine Press is authorized to publish and distribute exclusively the Chinese Simpli - fied Characters language edition .This edition is authorized for sale throughout Mainland of China . No part of the publication may be reproduced or distributed by any means ,or stored in a database or retrieval system ,without the prior written permiss...
Nederlandse norm NEN-EN-IEC 60754-1 ( en) Test on gases evolved during bustion of materials from cables -Part 1 :Determination of the halogen acid gas content ( IEC60754 - 1:2011,idt) ]]] Vervangt NEN-EN 50267-1 :1999 ,deels nen-en50267-2-1:1999.deels nen-en50267-2-2:1999,deels nen-en506-2-3:1999deels ics13.220.4029.02029.060.20 april 2014 document nas been under by DEKRA Certification edith cmrdkm55-20149-5441 NEN-EN-IEC 60754-1 Als Nederlandse norm is aanvaard -en60754-1:2014,idt iec60754-1:2011,DT Nederlands Elektrotechnisch Comite Normmissie 364020 " Draaden kabel voor elektrische sterkstroominstallaties (NEC20 ) THIS PUBLICATION IS COPYRIGHT PROTECTED DEZE PUBLICATIE IS AUTEURSRECHTELIJK BESCHERMD Apart from exceptions provided by the law ,nothing from this Although the utmost care has been taken with this publication may be duplicated and /orpublished by means of publication ,errors and omissions cannot be entirely photocopy ,microfilm ,storage in puter files or otherwise , excluded .The Netherlands Standardization Institute and /or which also applies to full or partial processing ,without the written the members of the mittees therefore accep...
EUROPEAN STANDARD en60601-2-34 NORME EUROPEENNE EUROPAISCHE NORM June 2014 ics11.040.55 Supersedes EN 60601-2-34 :2000 English Version Medical electrical equipment Part 2-34 :Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment (C60601-2-34:2011) Appareils electromedicaux-Partie 2-34 :Exigences Medizinische elektrische Gerate -Teil 2-34 :Besondere particulieres pour la securite de base et les performances Festlegungen fur die Sicherheit einschlielslich der essentielles des appareils de surveillance de la pression wesentlichen Leistungsmerkmale von invasiven Blutdruck - sanguine prelevee directement Uberwachungsgeraten (ce60601-2-34:2011) (e60601-2-34:2011) This European Standard was approved by CENELEC on 2011-05-16 .CENELEC members are bound to ply with the CEN /CENELEC Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CENELEC member This European Standa...
EN60436:2020(E) 6.4.7.1 General 6.5 Drying of the soiled tableware items 6.5.2 Oven drying method 6.5.3 Air drying method 6.6 Loading and operating 6.6.2 Operating Modification of Clause 7 " Combinedcleaning and drying performance assessment 7 Combined cleaning and drying performance assessment . 7.2 Determination of the drying performance 7.2.1 General requirements to enable subsequent cleaning assessment 7.2.2 Drying assessment procedure 7.2.3 Calculation of the drying index 7.3 Determination of the cleaning performance . 7.3.1 General . 7.3.4 Assessing In Wc Modification of clause 8 ," Energyconsumption ,water consumption ,cycle time and program time 8.1 General and purpose 8.2 Method of measurement 8.2.1 General 8.2.2 Energy consumption 8.2.4 Water consumption 8.2.5time. Modification of clause " Airborneacoustical noise 10 Modification of Annex A Annex A (normative)Placesettings and serving pieces A .2Test load specification 11 Modification of Annex B 12 Modification of Annex D 13 Modification of Annex E E .1General 14 Modification of Annex F F .1Specification of the microwave oven F .2Calibration of the microwave oven 15 Modification of Annex G G...