{"id":235957,"date":"2024-10-19T15:23:51","date_gmt":"2024-10-19T15:23:51","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-60601-2-222013\/"},"modified":"2024-10-25T10:00:04","modified_gmt":"2024-10-25T10:00:04","slug":"bs-en-60601-2-222013","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-60601-2-222013\/","title":{"rendered":"BS EN 60601-2-22:2013"},"content":{"rendered":"
Applies to the safety and essential performance of laser equipment for either surgical, therapeutic, medical diagnostic, cosmetic, or veterinary applications, intended for its use on humans or animals, classified as a class 3B or class 4 laser product as defined by 3.22 and 3.23 in IEC 60825-1, hereafter referred to as laser equipment. Throughout this International Standard, light emitting diodes (LED) are included whenever the word “laser” is used. This standard can also be applied to surgical, cosmetic, therapeutic and diagnostic laser equipment used for compensation or alleviation of disease, injury or disability. This third edition cancels and replaces the second edition of IEC 60601-2-22, published in 1995. This edition constitutes a technical revision. This third edition takes account of the recently published new editions of the General Standard IEC 60601-1 and publication IEC 60825-1. Additionally, it addresses technical and safety issues which have arisen in the time following the previous second edition.<\/p>\n
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
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8<\/td>\n | English CONTENTS <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | INTRODUCTION <\/td>\n<\/tr>\n | ||||||
10<\/td>\n | 201.1 Scope, object and related standards <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 201.2 Normative references 201.3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 201.4 General requirements 201.5 General requirements for testing me\u00a0equipment 201.6 Classification of me\u00a0equipment and me\u00a0systems 201.7 Me\u00a0equipment identification, marking and documents <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 201.8 Protection against electrical hazards from me equipment <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 201.9 Protection against mechanical hazards of me\u00a0equipment and me\u00a0systems 201.10 Protection against unwanted and excessive radiation hazards <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 201.11 Protection against excessive temperatures and other hazards <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 201.12 Accuracy of controls and instruments and protection against hazardous outputs <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | 201.13 Hazardous situations and fault conditions <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | 201.14 Programmable electrical medical systems (pems) 201.15 Construction of me\u00a0equipment <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 201.16 Me\u00a0systems 201.17 Electromagnetic compatibility of me\u00a0equipment and me\u00a0systems Annexes Annex D (informative) Symbols on marking Table D.1 \u2013 General symbols <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | Annex AA (informative) Particular guidance and rationale <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Medical electrical equipment – Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment<\/b><\/p>\n |