IEC 80601-2-77:2019
Medical electrical equipment - Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment
Medical electrical equipment - Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 111
- Дата публикации:
- 15 ноября 2023 г.
- Издание:
- IEC IS 80601 edition 1 version 1
- ICS:
- 11.040.01
IEC 80601-2-77:2019 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ROBOTICALLY ASSISTED SURGICAL EQUIPMENT (RASE) and ROBOTICALLY ASSISTED SURGICAL SYSTEMS (RASS), referred to as ME EQUIPMENT and ME SYSTEMS together with their INTERACTION CONDITIONS and INTERFACE CONDITIONS.
Abstract
Overview
IEC 80601-2-77:2019 is an international standard published by the International Electrotechnical Commission (IEC) that specifies particular requirements for the basic safety and essential performance of robotically assisted surgical equipment (RASE) and robotically assisted surgical systems (RASS). This standard applies to medical electrical equipment (ME equipment) and systems used in robotic surgery, ensuring their safe integration, reliable functioning, and compatibility within healthcare environments. The document consolidates crucial safety guidelines and performance criteria tailored specifically for robotic surgical technologies.
Key Topics
-
Scope and Applicability
IEC 80601-2-77:2019 targets the safety and performance demands necessary for robotically assisted surgical equipment and systems, covering their interaction and interface conditions with other medical devices and environments. -
Basic Safety Requirements
This standard emphasizes protection against electrical hazards, mechanical hazards, excessive radiation, temperature extremes, and other potential risks associated with robotic surgical devices. -
Essential Performance
It defines requirements to maintain the accuracy, reliability, and effectiveness of controls, instruments, and programmable electrical medical systems (PEMS) inherent in robotic-assisted surgical equipment. -
Testing and Evaluation Procedures
The standard prescribes rigorous testing methods to verify compliance with safety and performance criteria, including electromagnetic compatibility (EMC) testing and fault condition assessments. -
Identification and Documentation
Requirements for clear identification, marking, and comprehensive documentation of robotic surgical devices and systems are set to ensure proper use and traceability. -
Risk Assessment and Usability
It provides guidance on risk management, structural integrity testing throughout the expected service life, and usability considerations to minimize hazards during robotic surgical procedures.
Applications
IEC 80601-2-77:2019 is indispensable for manufacturers, designers, healthcare providers, and regulatory authorities involved with:
-
Robotically Assisted Surgery
Ensuring safety and performance of robotic surgical platforms used in minimally invasive procedures such as laparoscopic surgery, bone milling, and other complex operations. -
Medical Device Development
Guiding the architectural and functional design of new robotic surgical equipment to meet international safety standards before market release. -
Product Testing and Certification
Assisting testing laboratories and certification bodies in evaluating device compliance with standardized safety and performance standards required for global regulatory acceptance. -
Healthcare Facility Integration
Helping hospitals and surgical centers verify that robotic surgical equipment aligns with safety protocols for electrical, mechanical, and electromagnetic environments.
Related Standards
-
IEC 60601 Series
The broader medical electrical equipment standards family addressing general safety and performance requirements for all types of medical electrical devices. -
IEC 80601-2-x Series
Other particular standards within the 80601 series that target various specialized medical electrical systems and devices. -
ISO 13485
Quality management systems for medical device manufacturing, which supports implementing consistent safety and performance aligned with IEC standards. -
ISO/IEC Directives
Principles and rules governing the preparation and drafting of standards, including the collaboration framework between IEC and ISO, influencing the structure of IEC 80601-2-77.
Keywords: IEC 80601-2-77, robotically assisted surgical equipment, RASE, surgical robots, medical electrical equipment safety, essential performance, robotic surgery standards, medical device testing, medical system safety, healthcare regulatory standards, programmable electrical medical systems, electromagnetic compatibility, IEC medical standards.
Технические детали
- Технический комитет
- SC 62D - Particular medical equipment, software, and systems
- SKU
- IEC 80601-2-77:2019
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