{"id":236333,"date":"2024-10-19T15:25:27","date_gmt":"2024-10-19T15:25:27","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-60601-2-572011\/"},"modified":"2024-10-25T10:02:24","modified_gmt":"2024-10-25T10:02:24","slug":"bs-en-60601-2-572011","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-60601-2-572011\/","title":{"rendered":"BS EN 60601-2-57:2011"},"content":{"rendered":"
IEC 60601-2-57:2011 applies to basic safety and essential performance of equipment incorporating one or more sources of optical radiation in the wavelength range 200 nm to 3 000 nm, with the exception of laser radiation, and intended to create non-visual photo-biological effects in humans or animals for therapeutic, diagnostic, monitoring, cosmetic\/aesthetic or veterinary applications; hereafter referred to as light source equipment. IEC 60601-2-57:2011 does not apply to equipment for sun tanning, for ophthalmic instruments or for infant phototherapy. Light source equipment may consist of a single or multiple sources of optical radiation, with or without power supply, or may be incorporated into a complex system that includes optical, electricalor mechanical systems or sources of other radiation.<\/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 | ||||||
10<\/td>\n | INTRODUCTION <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | 201.1 Scope, object and related standards <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | 201.2 Normative references 201.3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 201.4 General requirements 201.5 General requirements for testing me\u00a0equipment 201.6 Classification of me\u00a0equipment and me systems <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 201.7 Me\u00a0equipment identification, marking and documents <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | Figure 201.101 \u2013 Example of explanatory label for a device with multiplehazard spectral regions <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 201.8 Protection against electrical hazards from me\u00a0equipment Figure 201.102 \u2013 Warning label \u2013 Hazard symbol <\/td>\n<\/tr>\n | ||||||
23<\/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 | ||||||
24<\/td>\n | 201.11 Protection against excessive temperatures and other hazards 201.12 Accuracy of controls and instruments and protection against hazardous outputs <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | 201.13 Hazardous situations and fault conditions <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | 201.14 Programmable electrical medical systems (pems) 201.15 Construction of me\u00a0equipment 201.16 Me\u00a0systems 201.17 Electromagnetic compatibility of me\u00a0equipment and me\u00a0systems Annexes <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | Annex\u00a0AA (informative)Particular guidance and rationale <\/td>\n<\/tr>\n | ||||||
29<\/td>\n | Annex\u00a0BB (informative)Exposure limit Values <\/td>\n<\/tr>\n | ||||||
33<\/td>\n | Annex\u00a0CC (informative)Protective eyewear for ls\u00a0equipment <\/td>\n<\/tr>\n | ||||||
34<\/td>\n | Annex\u00a0DD (informative)Summary of manufacturer\u2019s requirements <\/td>\n<\/tr>\n | ||||||
35<\/td>\n | Annex\u00a0EE (informative)Symbols on marking <\/td>\n<\/tr>\n | ||||||
36<\/td>\n | Bibliography <\/td>\n<\/tr>\n | ||||||
37<\/td>\n | Index of defined terms used in this particular standard <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Medical electrical equipment – Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic\/aesthetic use<\/b><\/p>\n |