BS EN IEC 60601-2-21:2021 – TC
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Tracked Changes. Medical electrical equipment – Particular requirements for the basic safety and essential performance of infant radiant warmers
Published By | Publication Date | Number of Pages |
BSI | 2021 | 116 |
IEC 60601-2-21:2020 is available as IEC 60601-2-21:2020 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.IEC 60601-2-21:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT RADIANT WARMERS as defined in 201.3.204, also referred to as ME EQUIPMENT. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this document are not covered by specific requirements in this document, except in 7.2.13 and 8.4.1 of the general standard. IEC 60601-2-21:2020 specifies the safety requirements for INFANT RADIANT WARMERS, but alternate methods of compliance with a specific clause, by demonstrating equivalent safety, will not be judged as non-compliant, if the MANUFACTURER has demonstrated in his RISK MANAGEMENT FILE that the RISK presented by the HAZARD has been found to be of an acceptable level when weighed against the benefit of treatment from the device. This particular standard does not apply to: – devices supplying heat via BLANKETS, PADS or MATTRESSES in medical use; for information, see IEC 60601-2-35; – INFANT INCUBATORS; for information, see IEC 60601-2-19; – INFANT TRANSPORT INCUBATORS, for information, see IEC 60601-2-20; – INFANT PHOTOTHERAPY EQUIPMENT, for information, see IEC 60601-2-50. SKIN TEMPERATURE SENSORS which are applied to operate a BABY CONTROLLED RADIANT WARMER including the displayed value are not considered to be a CLINICAL THERMOMETER in the sense of the particular standard ISO 80601-2-56. IEC 60601-2-21:2020 cancels and replaces the second edition published in 2009 and Amendment 1:2016. This edition constitutes a technical revision. IEC 60601-2-21:2020 includes the following significant technical change with respect to the previous edition: alignment with IEC 60601-1:2005 and IEC 60601-1:2005/AMD1:2012.
PDF Catalog
PDF Pages | PDF Title |
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74 | undefined |
77 | Annex ZA(normative)Normative references to international publicationswith their corresponding European publications |
79 | English CONTENTS |
80 | FOREWORD |
83 | INTRODUCTION |
84 | 201.1 Scope, object and related standards |
86 | 201.2 Normative references 201.3 Terms and definitions |
87 | Figure 201.101 – Layout of test devices |
88 | 201.4 General requirements Figure 201.102 – Test device |
89 | 201.5 General requirements for testing me equipment 201.6 Classification of me equipment and me systems 201.7 Me equipment identification, marking and documents Table 201.101 – Additional essential performance requirements |
91 | 201.8 Protection against electrical hazards from me equipment 201.9 Protection against mechanical hazards of me equipment and me systems |
93 | 201.10 Protection against unwanted and excessive radiation hazards 201.11 Protection against excessive temperatures and other hazards |
94 | 201.12 Accuracy of controls and instruments and protection against hazardous outputs |
98 | 201.13 Hazardous situations and fault conditions for me equipment 201.14 Programmable electrical medical systems (PEMS) 201.15 Construction of me equipment |
100 | 201.16 Me systems 201.17 Electromagnetic compatibility of me equipment and me systems 202 Electromagnetic disturbances – Requirements and tests |
101 | Annexes |
102 | Annex AA (informative) Particular guidance and rationale Figure AA.1 – Illustration of the main requirements of this document |
111 | Bibliography |
113 | Index of defined terms used in this document |