BS EN 62563-1:2010+A2:2021
Medical electrical equipment. Medical image display systems Evaluation methods
Standard number: | BS EN 62563-1:2010+A2:2021 |
Pages: | 78 |
Released: | 2021-09-01 |
ISBN: | 978 0 539 05720 1 |
Status: | Standard |
BS EN 62563-1:2010+A2:2021 Medical Electrical Equipment. Medical Image Display Systems Evaluation Methods
Standard Number: BS EN 62563-1:2010+A2:2021
Pages: 78
Released: 2021-09-01
ISBN: 978 0 539 05720 1
Name: Medical electrical equipment. Medical image display systems Evaluation methods
Status: Standard
Overview
The BS EN 62563-1:2010+A2:2021 standard is an essential document for professionals in the medical field, particularly those involved in the evaluation and maintenance of medical image display systems. This comprehensive standard provides detailed methods for assessing the performance and quality of medical electrical equipment, ensuring that medical image display systems meet the highest standards of accuracy and reliability.
Key Features
- Comprehensive Evaluation Methods: This standard outlines a variety of methods for evaluating the performance of medical image display systems, ensuring that all aspects of the system are thoroughly assessed.
- Up-to-Date Information: Released on 2021-09-01, this standard includes the latest amendments and updates, ensuring that you have the most current information available.
- Detailed Guidelines: With 78 pages of detailed guidelines, this standard provides in-depth information on the evaluation methods, making it an invaluable resource for professionals in the medical field.
- Internationally Recognized: As a BS EN standard, this document is recognized internationally, making it a reliable and authoritative source of information.
Why This Standard is Important
Medical image display systems are critical components in the healthcare industry, used for diagnosing and monitoring patients. Ensuring the accuracy and reliability of these systems is paramount, as any discrepancies can lead to misdiagnosis or incorrect treatment plans. The BS EN 62563-1:2010+A2:2021 standard provides a structured approach to evaluating these systems, helping to maintain high standards of patient care.
Who Should Use This Standard?
This standard is designed for a wide range of professionals in the medical field, including:
- Biomedical Engineers
- Medical Physicists
- Quality Assurance Professionals
- Healthcare Administrators
- Medical Device Manufacturers
Content Overview
The BS EN 62563-1:2010+A2:2021 standard is divided into several sections, each focusing on different aspects of medical image display systems evaluation. These sections include:
- Introduction: An overview of the standard and its objectives.
- Scope: Defines the scope of the standard and the types of medical image display systems it covers.
- Normative References: Lists the documents and standards referenced in the standard.
- Terms and Definitions: Provides definitions for key terms used throughout the standard.
- General Requirements: Outlines the general requirements for evaluating medical image display systems.
- Performance Evaluation: Detailed methods for evaluating the performance of medical image display systems, including tests for luminance, contrast, resolution, and more.
- Quality Assurance: Guidelines for implementing quality assurance programs to maintain the performance of medical image display systems.
- Annexes: Additional information and resources to support the evaluation methods outlined in the standard.
Benefits of Using This Standard
By adhering to the BS EN 62563-1:2010+A2:2021 standard, healthcare facilities can ensure that their medical image display systems are performing at their best, providing accurate and reliable images for diagnosis and treatment. Some of the key benefits include:
- Improved Patient Care: Accurate and reliable medical images are crucial for diagnosing and treating patients effectively. This standard helps ensure that medical image display systems provide high-quality images, leading to better patient outcomes.
- Compliance with Regulations: Adhering to this internationally recognized standard helps healthcare facilities comply with regulatory requirements, reducing the risk of non-compliance and potential penalties.
- Enhanced Quality Assurance: The detailed guidelines and evaluation methods provided in this standard help healthcare facilities implement robust quality assurance programs, ensuring the ongoing performance and reliability of their medical image display systems.
- Cost Savings: By maintaining the performance of medical image display systems, healthcare facilities can reduce the need for costly repairs and replacements, leading to significant cost savings over time.
Conclusion
The BS EN 62563-1:2010+A2:2021 standard is an invaluable resource for professionals in the medical field, providing comprehensive guidelines and evaluation methods for medical image display systems. By adhering to this standard, healthcare facilities can ensure the accuracy and reliability of their medical image display systems, leading to improved patient care and compliance with regulatory requirements. With its detailed guidelines and up-to-date information, this standard is a must-have for anyone involved in the evaluation and maintenance of medical image display systems.
BS EN 62563-1:2010+A2:2021
This standard BS EN 62563-1:2010+A2:2021 Medical electrical equipment. Medical image display systems is classified in these ICS categories:
- 11.040.55 Diagnostic equipment
This part of IEC 62563 describes the evaluation methods for testing medical image display systems.
The scope of this International Standard is directed to practical tests that can be visually evaluated or measured using basic test equipment. More advanced or more quantitative measurements can be performed on these devices, but these are beyond the scope of this document.
This standard applies to medical image display systems, which can display image information on greyscale and colour image display systems. This standard applies to medical image display systems used for diagnostic (interpretation of medical images toward rendering clinical diagnosis) or viewing (viewing medical images for medical purposes other than for providing a medical interpretation) purposes and therefore having specific requirements in terms of image quality. Head mounted image display systems and image display systems used for confirming positioning and for operation of the system are not covered by this standard. Handheld image display systems might require additional or modified versions of the procedures described in this standard.
It is not in the scope of this standard to define the requirements of acceptance and constancy tests or the frequencies of constancy tests.