Medical electrical equipment — Part 2-74: Particular requirements for basic safety and essential per...
This document applies to the basic safety and essential performance of a humidifier, also hereafter referred to as ME equipment, in combination with its accessories, the combination also hereafter referred to as ME system.
This document is also applicable to those accessories intended by their manufacturer to be connected to a humidifier where the characteristics of those accessories can affect…
Medical electrical equipment — Part 2-90: Particular requirements for basic safety and essential per...
This document applies to the basic safety and essential performance of respiratory high-flow therapy equipment, as defined in 201.3.220, hereafter also referred to as ME equipment or ME system, in combination with its accessories:
— intended for use with patients who can breathe spontaneously; and
— intended for patients who would benefit from improved alveolar gas exchange; and who would…
Oil and gas industries including lower carbon energy — Well integrity — Life cycle governance
ISO 16530-1:2017 is applicable to all wells that are operated by the petroleum and natural gas industry. This document is applicable to any well, or group of wells, regardless of their age, location (including onshore, subsea and offshore wells) or type (e.g. naturally flowing, artificial lift, injection wells).
ISO 16530-1:2017 is intended to assist the petroleum and natural gas industry to…
Commercial beverage coolers — Classification, requirements and test conditions
This document specifies the classification for commercial beverage coolers and their requirements and test methods. This document is applicable to integral refrigeration systems.
This document is not applicable to remote and secondary system cabinets.
Space systems — Launch-vehicle-to-spacecraft interfaces
ISO 14303 specifies the interfaces between a launch vehicle (LV) and the spacecraft (SC) being launched, to provide LV and SC organizations with the necessary format for presenting the required technical data on existing and future interfaces. Its intended purpose is to minimize costs and reduce the risks from errors resulting from miscommunication. It does not limit the ability of LV or SC…
Medical electrical equipment — Clinical performance evaluation of clinical thermometers
This document specifies the requirements and methods for the clinical investigation of ME equipment used to measure the body temperature in indirect measurement mode.
This document covers both intermittently and continuously measuring clinical thermometers.
NOTE For clinical thermometers in direct measurement mode determining the technical accuracy in accordance with IEC 80601-2-56 is…
Exactitude (justesse et fidélité) des résultats et méthodes de mesure — Partie 2: Méthode de base po...
1.1 Le présent document:
— souligne les principes généraux applicables à la planification d'expériences pour l'estimation numérique de la fidélité des méthodes de mesure au moyen d'une expérience collaborative interlaboratoires;
— fournit une description pratique détaillée de la méthode de base d'une utilisation courante pour l'estimation de la fidélité des méthodes de…
Information technology — Office equipment — Method for the determination of toner cartridge yield fo...
ISO/IEC 19752:2017 is limited to the evaluation of toner cartridge page yield for toner containing cartridges (i.e. all-in-one toner cartridges and toner cartridges without a photoconductor) for monochrome electrophotographic print systems. This document could also be applied to the printer component of any multifunctional device that has a digital input-printing path (i.e. multi-function devices…
Nanotechnologies — A test method for detection of nano-object(s) release from mask media
This TS specifies a test method for detection of nano-object/s release from respiratory masks media containing nanomaterial/s under different (light, medium and heavy) working conditions. In addition this standard also provides the sampling procedure and qualitative characterization methods of the released nano-object/s. The document does not consider the health and safety aspects of the released…
