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 ISO 27427

Anaesthetic and respiratory equipment — Nebulizing systems and components

inactive
Buy Now
Organization: BSI
Publication Date: 28 February 2014
Status: inactive
Page Count: 60
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

BS EN ISO 27427
July 31, 2023
Anaesthetic and respiratory equipment - Nebulizing systems and components
A description is not available for this item.
BS ISO 27427
February 28, 2014
Anaesthetic and respiratory equipment — Nebulizing systems and components
A description is not available for this item.
BS EN ISO 27427
February 28, 2014
Anaesthetic and respiratory equipment - Nebulizing systems and components
A description is not available for this item.

References

This document references:
IEC 60601-1-6 - Medical electrical equipment – Part 1-6: General requirements for basic safety and essential performance – Collateral standard: Usability
Published by IEC on July 1, 2020
This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL...
This document references:
11607-1 AMD 1 - Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems AMENDMENT 1: Application of risk management
Published by ISO on September 1, 2023
A description is not available for this item.
This document references:
ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on August 15, 2006
Inclusions This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE Although the scope of this...
This document references:
ISO 10993-15 - Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys
Published by ISO on November 1, 2019
This document specifies general requirements for the design of tests for identifying and quantifying degradation products from final metallic medical devices or corresponding material samples...
This document references:
IEC 60601-1-6 - Medical electrical equipment – Part 1-6: General requirements for basic safety and essential performance – Collateral standard: Usability
Published by IEC on July 1, 2020
This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL...
View Less
View All
Advertisement