BS EN 60601-2-17:2015
$198.66
Medical electrical equipment – Particular requirements for the basic safety and essential performance of automatically-controlled brachytherapy afterloading equipment
Published By | Publication Date | Number of Pages |
BSI | 2015 | 54 |
IEC 60601-2-17:2013 applies to the basic safety and essential performance of automatically-controlled Brachytherapy Afterloading Medical Equipment. This standard does not specify requirements for sealed radioactive sources. This third edition cancels and replaces the second edition, published in 2004. Consideration has been given to new IEC standards, amendments to existing IEC standards, developments in technology and clinical usage, and various hazards encountered and envisaged since the preparation of the first and second editions. This edition constitutes a technical revision which brings this standard in line with IEC 60601-1:2005+A1:2012 and its collateral standards.
PDF Catalog
PDF Pages | PDF Title |
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4 | Foreword Endorsement notice |
5 | Annex ZA (normative) Normative references to international publications with their corresponding European publications |
7 | Annex ZZ (informative) Coverage of Essential Requirements of EU Directives |
8 | English CONTENTS |
9 | FOREWORD |
12 | INTRODUCTION |
13 | 201.1 Scope, object and related standards |
15 | 201.2 Normative references |
16 | 201.3 Terms and definitions |
18 | 201.4 General requirements 201.5 General requirements for testing ME EQUIPMENT 201.6 Classification of ME EQUIPMENT and ME SYSTEMS |
19 | 201.7 ME EQUIPMENT identification, marking and documents |
20 | Table 201.101 – Colours of lights and their meanings |
23 | Protection against electrical 201.8 HAZARDS from ME EQUIPMENT |
24 | 201.9 Protection against MECHANICAL HAZARDS of ME EQUIPMENT andME SYSTEMS 201.10 Protection against unwanted and excessive radiation HAZARDS |
43 | 201.11 Protection against excessive temperatures and other HAZARDS 201.12 Accuracy of controls and instruments and protection againsthazardous outputs |
46 | HAZARDOUS SITUATIONS and fault conditions 201.13 for ME EQUIPMENT 201.14 PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS (PEMS) 201.15 Construction of ME EQUIPMENT 201.16 ME SYSTEMS 201.17 Electromagnetic compatibility of ME EQUIPMENT and ME SYSTEMS |
47 | Annex A (informative)General guidance and rationale |
48 | Bibliography |
49 | Index of defined terms used in this particular standard |