BS EN IEC 63009:2019
Ultrasonics. Physiotherapy systems. Field specifications and methods of measurement in the frequency range 20 kHz to 500 kHz
| Standard number: | BS EN IEC 63009:2019 |
| Pages: | 42 |
| Released: | 2019-09-23 |
| ISBN: | 978 0 580 94831 2 |
| Status: | Standard |
BS EN IEC 63009:2019 Ultrasonics Physiotherapy Systems
Discover the essential standard for ultrasonics in physiotherapy systems with the BS EN IEC 63009:2019. This comprehensive document provides detailed field specifications and methods of measurement for systems operating within the frequency range of 20 kHz to 500 kHz. Released on September 23, 2019, this standard is a crucial resource for professionals in the field of physiotherapy and medical device manufacturing.
Key Features
- Standard Number: BS EN IEC 63009:2019
- Pages: 42
- Release Date: September 23, 2019
- ISBN: 978 0 580 94831 2
- Status: Standard
Comprehensive Coverage
This standard is meticulously crafted to ensure that all aspects of ultrasonics in physiotherapy systems are covered. It provides a robust framework for understanding the field specifications and the precise methods of measurement required for systems operating in the specified frequency range. Whether you are a manufacturer, a healthcare provider, or a researcher, this document is indispensable for ensuring compliance and enhancing the quality of ultrasonic physiotherapy systems.
Why This Standard Matters
Ultrasonics play a pivotal role in modern physiotherapy, offering non-invasive treatment options that can significantly enhance patient outcomes. The BS EN IEC 63009:2019 standard ensures that these systems are designed and operated to the highest standards, promoting safety, efficacy, and reliability. By adhering to this standard, manufacturers can ensure that their products meet international benchmarks, thereby gaining trust and credibility in the global market.
Applications and Benefits
The applications of this standard are vast, encompassing various aspects of physiotherapy and rehabilitation. By following the guidelines set forth in this document, practitioners can optimize the therapeutic benefits of ultrasonic treatments, ensuring that patients receive the best possible care. Additionally, the standard aids in the development of new technologies and innovations in the field, paving the way for advanced treatment modalities.
Technical Insights
The BS EN IEC 63009:2019 standard delves into the technical intricacies of ultrasonic physiotherapy systems, providing detailed methodologies for measurement and evaluation. It covers the entire spectrum of frequencies from 20 kHz to 500 kHz, ensuring comprehensive guidance for all relevant systems. This level of detail is crucial for engineers and designers who are tasked with creating cutting-edge devices that meet stringent regulatory requirements.
Global Relevance
As a part of the IEC (International Electrotechnical Commission) standards, the BS EN IEC 63009:2019 is recognized globally, making it a vital resource for international companies and organizations. Its adoption ensures that products are not only compliant with local regulations but also meet the expectations of a global market. This standard is a testament to the commitment to quality and safety in the field of medical ultrasonics.
Conclusion
In conclusion, the BS EN IEC 63009:2019 standard is an essential document for anyone involved in the design, manufacture, or application of ultrasonic physiotherapy systems. Its comprehensive guidelines and specifications provide a solid foundation for ensuring that these systems are safe, effective, and reliable. By adhering to this standard, stakeholders can contribute to the advancement of physiotherapy technologies and improve patient care worldwide.
BS EN IEC 63009:2019
This standard BS EN IEC 63009:2019 Ultrasonics. Physiotherapy systems. Field specifications and methods of measurement in the frequency range 20 kHz to 500 kHz is classified in these ICS categories:
- 17.140.50 Electroacoustics
- 11.040.60 Therapy equipment
This document only relates to ultrasonic physiotherapy equipment employing a single plane non-focusing circular transducer per treatment head, producing static beams perpendicular to the face of the treatment head.
This document specifies:
• methods of measurement and characterization of the output of ultrasonic physiotherapy equipment based on reference testing methods;
• characteristics to be specified by manufacturers of ultrasonic physiotherapy equipment;
• methods of measurement and characterization of the output of ultrasonic physiotherapy equipment based on routine testing methods;
• acceptance criteria for aspects of the output of ultrasonic physiotherapy equipment.
The therapeutic value and methods of use of ultrasonic physiotherapy equipment are not within the scope of this document.
Excluded equipment includes, but is not limited to:
• equipment in which ultrasound waves are intended to destroy conglomerates (for example stones in the kidneys or the bladder) or tissue of any type;
• equipment in which a tool is driven by ultrasound (for example surgical scalpels, phacoemulsifiers, dental scalers or intracorporeal lithotripters);
• equipment in which ultrasound waves are intended to sensitize tissue to further therapies (for example radiation or chemotherapy);
• equipment in which ultrasound waves are intended to treat cancerous (i.e., malignant) or pre-cancerous tissue, or benign masses, such as High Intensity Focused Ultrasound (HIFU) or High Intensity Therapeutic Ultrasound (HITU).