IEC 80601-2-78:2019
Medical electrical equipment - Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation
Medical electrical equipment - Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 156
- Дата публикации:
- 12 марта 2024 г.
- Издание:
- IEC IS 80601 edition 1 version 1
- ICS:
- 11.040.01
IEC 80601-2-78:2019 applies to the general requirements for BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ROBOTS that physically interact with a PATIENT with an IMPAIRMENT to support or perform REHABILITATION, ASSESSMENT, COMPENSATION or ALLEVIATION related to the PATIENT’S MOVEMENT FUNCTIONS, as intended by the MANUFACTURER. IEC 80601-2-78:2019 does not apply to • external limb prosthetic devices (use ISO 22523), • electric wheelchairs (use ISO 7176 (all parts)), • diagnostic imaging equipment (e.g. MRI, use IEC 60601-2-33), and • personal care ROBOTS (use ISO 13482).
Abstract
Overview
IEC 80601-2-78:2019 is an international standard published by the International Electrotechnical Commission (IEC) that specifies particular requirements for the basic safety and essential performance of medical robots used in rehabilitation, assessment, compensation, or alleviation of movement impairments. This standard ensures that medical electrical equipment in the form of rehabilitation robots meets rigorous safety and functionality criteria when interacting physically with patients.
The scope of IEC 80601-2-78:2019 covers medical robots designed to assist patients with movement-related impairments. It establishes a framework for evaluating risks and performance to enhance patient safety and device reliability. However, this standard does not apply to external limb prosthetic devices, electric wheelchairs, diagnostic imaging equipment, or personal care robots, which are covered by other specialized standards such as ISO 22523, ISO 7176, IEC 60601-2-33, and ISO 13482 respectively.
Key Topics
-
Basic Safety Requirements
IEC 80601-2-78:2019 mandates protection from electrical, mechanical, and radiation hazards related to medical rehabilitation robots. It addresses potential hazards that could arise during the operation of these devices to safeguard patients and operators. -
Essential Performance Criteria
The standard defines essential performance attributes necessary to ensure that rehabilitation robots operate as intended. This includes accuracy of control systems, reliability of sensors, and maintaining functionality under various operational conditions. -
Risk Management and Usability
Emphasizing patient safety, the document incorporates risk management processes aligning with ISO 14971 and usability engineering in accordance with IEC 62366-1. This ensures that design decisions consider potential risk factors and support user-friendly interfaces for patients and healthcare providers. -
Testing and Validation
IEC 80601-2-78 outlines specific testing methods to verify electrical safety, mechanical integrity, electromagnetic compatibility, and alarm system functions. These tests confirm that rehabilitation robots meet stringent quality and safety benchmarks before clinical use. -
Programmable Electrical Medical Systems (PEMS)
The standard includes requirements for programmable aspects of medical robots to ensure software reliability and safe operation during adaptive or autonomous functioning.
Applications
IEC 80601-2-78:2019 is applicable to a broad range of medical robots engaged in:
-
Rehabilitation
Robots designed to support patient recovery and physical therapy by facilitating movement exercises or neuromuscular retraining. -
Assessment
Devices that measure and evaluate patient movement capabilities to inform clinicians about functional impairments and recovery progress. -
Compensation
Assistive robots that help patients perform movements they are unable to complete independently, aiding daily living activities. -
Alleviation
Systems aimed at reducing the impact of movement disabilities through external support or adaptive technologies.
This standard is critical for manufacturers developing rehabilitation robots ensuring compliance with internationally recognized safety norms, enabling market access worldwide, and enhancing patient outcomes.
Related Standards
- ISO 22523 – Requirements for external limb prosthetic devices
- ISO 7176 (all parts) – Standards for electric wheelchairs
- IEC 60601-2-33 – Particular requirements for diagnostic imaging equipment such as MRI
- ISO 13482 – Safety requirements for personal care robots
- ISO 14971 – Medical device risk management
- IEC 62366-1 – Usability engineering for medical devices
By adhering to IEC 80601-2-78:2019, manufacturers integrate robust safety and performance protocols within medical robotics, fostering reliable assistive technologies that support patient mobility and functional independence. The standard plays a pivotal role in defining best practices for the safe development, deployment, and clinical use of rehabilitation robotics worldwide.
Технические детали
- Технический комитет
- SC 62D - Particular medical equipment, software, and systems
- SKU
- IEC 80601-2-78:2019
Похожие стандарты
Стандарты, упомянутые в описании
BS EN ISO 22523:2006
ДействующийExternal limb prostheses and external orthoses. Requirements and test methods.
ISO 7176-6:2018
ДействующийWheelchairs — Part 6: Determination of maximum speed of electrically powered wheelchairs
Overview ISO 7176-6:2018 specifies uniform test methods to determine the maximum speed of electrically powered wheelchairs, including scooters, intended to carry one person with a nominal maximum spe…
IEC 60601-2-33:2010
ДействующийMedical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performa…
Overview IEC 60601-2-33:2010 is an international standard developed by the International Electrotechnical Commission (IEC) that specifies the particular basic safety and essential performance require…
BS EN ISO 13482:2014
ДействующийRobots and robotic devices. Safety requirements for personal care robots.
ISO 14971:2007
ДействующийMedical devices - Application of risk management to medical devices
Overview ISO 14971:2007 - Medical devices - Application of risk management to medical devices - defines a systematic process for identifying hazards, estimating and evaluating risks, implementing ris…
IEC 62366-1:2015
ДействующийMedical devices - Part 1: Application of usability engineering to medical devices
Overview IEC 62366-1:2015 is an international standard published by the International Electrotechnical Commission (IEC) that defines the process for applying usability engineering-also known as human…