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BS EN 60601-2-43:2022 – TC:2023 Edition

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Tracked Changes. Medical electrical equipment – Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures

Published By Publication Date Number of Pages
BSI 2023 176
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This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of both FIXED and MOBILE X-RAY EQUIPMENT declared by the MANUFACTURER to be suitable for RADIOSCOPICALLY GUIDED INTERVENTIONAL PROCEDURES, hereafter referred to as INTERVENTIONAL X-RAY EQUIPMENT. Its scope excludes, in particular: – equipment for RADIOTHERAPY; – equipment for COMPUTED TOMOGRAPHY; – ACCESSORIES intended to be introduced into the PATIENT; – mammographic X-RAY EQUIPMENT; – dental X-RAY EQUIPMENT. NOTE 1 Examples of RADIOSCOPICALLY GUIDED INTERVENTIONAL PROCEDURES, for which the use of INTERVENTIONAL X-RAY EQUIPMENT complying with this standard is recommended, are given in Annex AA. NOTE 2 Specific requirements for magnetic navigation devices, and for the use of INTERVENTIONAL X-RAY EQUIPMENT in an operating room environment were not considered in this particular standard; therefore no specific requirements have been developed for these devices or uses. In any case, such devices or uses remain under the general clause requirements. NOTE 3 INTERVENTIONAL X-RAY EQUIPMENT, when used for cone-beam CT mode, is covered by this standard and not by IEC 60601-2-44 [2]2. No additional requirements for operation in cone-beam CT mode were identified for this standard (see also Note 4 in 203.6.4.5). INTERVENTIONAL X-RAY EQUIPMENT declared by the MANUFACTURER to be suitable for RADIOSCOPICALLY GUIDED INTERVENTIONAL PROCEDURES, which does not include a PATIENT SUPPORT as part of the system, is exempt from the PATIENT SUPPORT provisions of this standard. If a clause or subclause is specifically intended to be applicable to INTERVENTIONAL X-RAY 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 INTERVENTIONAL X-RAY EQUIPMENT and to ME SYSTEMS, as relevant. NOTE 4 See also 4.2 of the general standard. The subclauses of this standard supersede IEC 60601-2-54 subclauses. IEC 60601-2-54 applies only with regards to the cited subclauses; non-cited subclauses of IEC 60601-2-54 do not apply.

PDF Catalog

PDF Pages PDF Title
107 undefined
112 Annex ZA (normative)Normative references to international publicationswith their corresponding European publications
115 Blank Page
116 English
CONTENTS
117 FOREWORD
120 INTRODUCTION
121 201.1 Scope, object and related standards
123 201.2 Normative references
124 201.3 Terms and definitions
125 201.4 General requirements
Table 201.101 – Additional list of potential essential performance to be considered by the manufacturer in the risk management analysis
127 201.5 General requirements for testing me equipment
201.6 Classification of me equipment and me systems
201.7 Me equipment identification, marking and documents
131 201.8 Protection against electrical hazards from me equipment
Table 201.102 – Other subclauses requiring statements in accompanying documents
132 201.9 Protection against mechanical hazards of me equipment and me systems
133 201.10 Protection against unwanted and excessive radiation hazards
201.11 Protection against excessive temperatures and other hazards
135 201.12 Accuracy of controls and instruments and protection against hazardous outputs
138 201.13 Hazardous situations and fault conditions for me equipment
201.14 Programmable electrical medical systems (PEMS)
139 201.15 Construction of me equipment
201.16 ME Systems
201.17 Electromagnetic compatibility of me equipment and me systems
140 202 Electromagnetic disturbances – Requirements and tests
203 Radiation protection in diagnostic x-ray equipment
153 Annexes
154 Annex AA (informative) Particular guidance and rationale
Table AA.1 – Examples of prolonged radioscopically guided interventional procedures for which deterministic effects of irradiation are possible
155 Table AA.2 – Examples of radioscopically guided interventional procedures for which deterministic effects are unlikely
164 Table AA.3 – Examples of isodose boundaries and colour codes for skin dose map and air kerma map
166 Annex BB (normative) Distribution maps of stray radiation
167 Figure BB.1 – Example of isokerma map at 100 cm height in lateral configuration
168 Figure BB.2 – Example of isokerma map at 100 cm height in vertical configuration
169 Bibliography
172 Index of defined terms
BS EN 60601-2-43:2022 - TC
$258.95