BS EN 60601-2-57:2011
$167.15
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
Published By | Publication Date | Number of Pages |
BSI | 2011 | 40 |
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.
PDF Catalog
PDF Pages | PDF Title |
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8 | English CONTENTS |
10 | INTRODUCTION |
11 | 201.1 Scope, object and related standards |
13 | 201.2 Normative references 201.3 Terms and definitions |
16 | 201.4 General requirements 201.5 General requirements for testing me equipment 201.6 Classification of me equipment and me systems |
18 | 201.7 Me equipment identification, marking and documents |
21 | Figure 201.101 – Example of explanatory label for a device with multiplehazard spectral regions |
22 | 201.8 Protection against electrical hazards from me equipment Figure 201.102 – Warning label – Hazard symbol |
23 | 201.9 Protection against mechanical hazards of me equipment and me systems 201.10 Protection against unwanted and excessive radiation hazards |
24 | 201.11 Protection against excessive temperatures and other hazards 201.12 Accuracy of controls and instruments and protection against hazardous outputs |
25 | 201.13 Hazardous situations and fault conditions |
26 | 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 Annexes |
27 | Annex AA (informative)Particular guidance and rationale |
29 | Annex BB (informative)Exposure limit Values |
33 | Annex CC (informative)Protective eyewear for ls equipment |
34 | Annex DD (informative)Summary of manufacturer’s requirements |
35 | Annex EE (informative)Symbols on marking |
36 | Bibliography |
37 | Index of defined terms used in this particular standard |