BS 5724-1:1979 - Comprehensive Guide to Health Care Technology Standards

The BS 5724-1:1979 is a pivotal standard in the realm of health care technology, focusing on safety and performance criteria for medical electrical equipment. This British Standard emphasizes the importance of compliance with the specified safety requirements, ensuring that medical devices are not only effective but also safe for patient use.

Originally modified from IEC 60601-1:1977, this standard was published on March 30, 1979, and it serves as a critical framework that guides manufacturers and healthcare providers in the development and implementation of medical technologies.

As the industry steadily progresses towards greater innovations in health care technology, maintaining adherence to these standards becomes increasingly essential. BS 5724-1:1979 outlines specific testing protocols and performance metrics, safeguarding health care practitioners and patients alike from unnecessary risks associated with medical electrical equipment.

Key Specifications

• Health Care Technology Index: 11
• Modified Standard: IEC 60601-1:1977
• Publication Date: 1979-03-30
• Format: Hardcopy
• Replacements: This standard was eventually replaced by the dual-numbered standard BS EN 60601-1:1990 and BS 5724-1:1989.

For professionals engaged in the design, manufacture, and quality assurance of medical electrical equipment, the BS 5724-1:1979 standard is an essential resource. With a price point of £330.00, it provides invaluable insights into compliance requirements that can aid in avoiding potential liabilities and enhancing overall product safety.

Acquiring the hardcopy version of this standard means you have a tangible resource at your disposal, which is beneficial for cross-referencing during design and compliance evaluations. Adhering to such outlined standards promotes a consistent approach to healthcare technology, fostering advancements that prioritize patient safety and device reliability.

By staying informed with BS 5724-1:1979, organizations can assure their products meet national and international safety benchmarks, ultimately contributing to improved patient outcomes and enhanced trust in medical innovations.