BS EN 60601-2-43:2022

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

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Standard number:	BS EN 60601-2-43:2022
Pages:	70
Released:	2023-01-25
ISBN:	978 0 539 19751 8
Status:	Standard

BS EN 60601-2-43:2022 Medical Electrical Equipment - Essential Safety and Performance Requirements for X-ray Equipment for Interventional Procedures

Introducing the BS EN 60601-2-43:2022, a comprehensive standard that outlines the particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures. This standard is a must-have for all professionals in the medical field, especially those who are involved in the use and maintenance of X-ray equipment.

Released on 25th January 2023, this standard is the latest in the field, ensuring that you are up-to-date with the most recent safety and performance requirements. With a total of 70 pages, it provides an in-depth guide to the safe and effective use of X-ray equipment in interventional procedures.

Key Features

The BS EN 60601-2-43:2022 standard is packed with essential information and guidelines that are crucial for the safe and effective operation of X-ray equipment. Here are some of its key features:

Comprehensive Coverage: With 70 pages of detailed information, this standard provides a thorough overview of the safety and performance requirements for X-ray equipment.
Up-to-Date Information: Released in 2023, this standard contains the most recent guidelines, ensuring that you are in compliance with the latest safety and performance standards.
Easy to Understand: The standard is written in clear, concise language, making it easy for professionals of all levels to understand and implement the guidelines.

Who Should Use This Standard?

The BS EN 60601-2-43:2022 standard is designed for a wide range of professionals in the medical field. This includes:

Medical practitioners who use X-ray equipment for interventional procedures.
Healthcare facility managers responsible for the maintenance and safety of X-ray equipment.
Medical equipment manufacturers who need to ensure their products meet the latest safety and performance standards.

Why Choose BS EN 60601-2-43:2022?

Choosing the BS EN 60601-2-43:2022 standard means choosing a commitment to safety and performance. This standard ensures that you are using and maintaining your X-ray equipment in accordance with the latest guidelines, reducing the risk of accidents and improving the effectiveness of your procedures.

With its comprehensive coverage and easy-to-understand language, the BS EN 60601-2-43:2022 standard is an invaluable resource for all professionals in the medical field. Don't compromise on safety and performance - choose the BS EN 60601-2-43:2022 standard today.

Order your copy now and ensure your X-ray equipment meets the highest standards of safety and performance. The standard is available in print and digital formats and can be ordered using the ISBN number 978 0 539 19751 8.

Stay ahead of the curve with the BS EN 60601-2-43:2022 standard - your guide to the safe and effective use of X-ray equipment for interventional procedures.

DESCRIPTION

BS EN 60601-2-43:2022

This standard BS EN 60601-2-43:2022 Medical electrical equipment is classified in these ICS categories:

11.040.50 Radiographic equipment
37.040.25 Radiographic films

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.

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