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.

ISO 26782 FRENCH

Matériel d'anesthésie et de réanimation respiratoire - Spiromètres destinés au mesurage des volumes expiratoires forcés chronométrés chez les humains Rectificatif technique 1

active, Most Current
Buy Now
Organization: ISO
Publication Date: 15 November 2009
Status: active
Page Count: 1
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

ISO 26782 FRENCH
November 15, 2009
Matériel d'anesthésie et de réanimation respiratoire - Spiromètres destinés au mesurage des volumes expiratoires forcés chronométrés chez les humains Rectificatif technique 1
A description is not available for this item.
ISO 26782 FRENCH
July 15, 2009
Matériel d'anesthésie et de réanimation respiratoire - Spiromètres destinés au mesurage des volumes expiratoires forcés chronométrés chez les humains
A description is not available for this item.

References

This document references:
ISO 13485 - Medical devices - Quality management systems - Requirements for regulatory purposes
Published by ISO on March 1, 2016
This International Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that...
This document references:
ISO 14937 - Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Published by ISO on October 15, 2009
Inclusions This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a...
This document references:
ISO 14971 - Medical devices - Application of risk management to medical devices
Published by ISO on December 1, 2019
This document specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The process...
This document references:
ISO 23747 - Anaesthetic and respiratory equipment - Peak expiratory flow meters for the assessment of pulmonary function in spontaneously breathing humans
Published by ISO on August 1, 2015
This International Standard specifies requirements for a peak expiratory flow meter (pefm) intended for the assessment of pulmonary function in spontaneously breathing humans. This International...
This document references:
IEC 60601-1 - MEDICAL ELECTRICAL EQUIPMENT – Part 1: General requirements for basic safety and essential performance
Published by IEC on March 1, 2021
A description is not available for this item.
This document references:
15223-1 - Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements
Published by ISO on July 1, 2021
This document specifies symbols used to express information supplied for a medical device. This document is applicable to symbols used in a broad spectrum of medical devices, that are available...
View Less
View All
Advertisement