UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

BSI - BS EN ISO 80601-2-12

Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators

active, Most Current
Organization: BSI
Publication Date: 30 November 2023
Status: active
Page Count: 170
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

BS EN ISO 80601-2-12
November 30, 2023
Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
A description is not available for this item.
BS EN ISO 80601-2-12
March 31, 2020
Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
A description is not available for this item.
BS EN ISO 80601-2-12
September 30, 2011
Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
To be read in conjunction with BS EN 60601-1
BS EN ISO 80601-2-12
September 30, 2011
Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
A description is not available for this item.

References

This document references:
AAMI 2700-1 - Medical Devices and Medical Systems - Essential safety and performance requirements for equipment comprising the patient-centric integrated clinical environment (ICE) - Part 1: General requirements and conceptual model
Published by AAMI on January 1, 2019
This standard specifies general requirements, a model and framework for integrating equipment to create a INTEGRATED CLINICAL ENVIRONMENT (ICE), as defined in 3.6. This standard specifies the...
This document references:
IEC 60068-2-27 - Environmental testing – Part 2-27: Tests – Test Ea and guidance: Shock
Published by IEC on February 1, 2008
Object To provide a standard procedure for determining the ability of a specimen to withstand specified severities of shock.
This document references:
IEC 60068-2-31 - Environmental testing – Part 2-31: Tests – Test Ec: Rough handling shocks, primarily for equipment-type specimens
Published by IEC on May 1, 2008
This part of IEC 60068 deals with a test procedure for simulating the effects of rough handling shocks, primarily in equipment-type specimens, the effects of knocks, jolts and falls which may be...
This document references:
IEC 60601-1-10 - Medical electrical equipment – Part 1-10: General requirements for basic safety and essential performance – Collateral Standard: Requirements for the development of physiologic closed-loop controllers
Published by IEC on July 1, 2020
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document references:
IEC 60601-1-12 - Medical electrical equipment – Part 1-12: General requirements for basic safety and essential performance – Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment
Published by IEC on July 1, 2020
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS,...
This document is referenced by:
EN ISO 80601-2-55 - Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors
Published by CEN on February 1, 2018
This document specifies particular requirements for the BASIC SAFETY and ESSENTIAL PERFORMANCE of a RESPIRATORY GAS MONITOR (RGM), hereafter referred to as ME EQUIPMENT, intended for CONTINUOUS...
View Less
View All
Advertisement