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 - 23/30475022 DC

Draft BS EN ISO 80601-2-90 Medical electrical equipment Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment

pending
Organization: BSI
Publication Date: 4 July 2023
Status: pending
Page Count: 116
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

23/30475022 DC
July 4, 2023
Draft BS EN ISO 80601-2-90 Medical electrical equipment Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment
A description is not available for this item.
BS EN ISO 80601-2-90
October 31, 2021
Medical electrical equipment Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment
A description is not available for this item.

References

This document references:
IEC 60601-1-3 - Medical electrical equipment – Part 1-3: General requirements for basic safety and essential performance – Collateral Standard: Radiation protection in diagnostic X-ray equipment
Published by IEC on January 1, 2021
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 61672-1 - Electroacoustics - Sound level meters - Part 1: Specifications
Published by IEC on September 1, 2013
This part of IEC 61672 gives electroacoustical performance specifications for three kinds of sound measuring instruments: a time-weighting sound level meter that measures exponential-time-weighted,...
This document references:
IEC 62366-1 - Medical devices – Part 1: Application of usability engineering to medical devices
Published by IEC on June 1, 2020
This part of IEC 62366 specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY of a MEDICAL DEVICE as it relates to SAFETY. This USABILITY ENGINEERING (HUMAN...
This document references:
IEC 62570 - Standard practice for marking medical devices and other items for safety in the magnetic resonance environment
Published by IEC on February 1, 2014
A description is not available for this item.
This document references:
81001-5-1 - Health software and health IT systems safety, effectiveness and security – Part 5-1: Security – Activities in the product life cycle
Published by IEC on December 1, 2021
This document defines the LIFE CYCLE requirements for development and maintenance of HEALTH SOFTWARE needed to support conformance to IEC 62443-4-1[11] – taking the specific needs for HEALTH SOFTWARE...
View Less
View All
Advertisement