Document management — Electronically stored information — Requirements for trustworthiness and relia...
This document specifies the implementation and operation of information management systems that stores and make available for use electronically stored information (ESI) in a trustworthy and reliable manner. Such ESI can be of any type, including “page based” information, information in databases and audio/video information.
This document is for use by any organization that uses information…
The provisions of this document apply to Single-Stage and economised refrigerant compressors of the positive displacement type. Selected test methods are described for the determination of the refrigerating capacity, the power, the isentropic efficiency and the coefficient of performance. These test methods provide results of sufficient accuracy to permit consideration of the suitability of a…
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…
Medical devices — Information to be supplied by the manufacturer
NOTE 1 There is guidance or rationale for this Clause contained in Clause A.2.
This document specifies the requirements for information supplied by the manufacturer for a medical device or by the manufacturer for an accessory, as defined in 3.1. This document includes the generally applicable requirements for identification and labels on a medical device or accessory, the packaging,…
Information technology — Coding-independent code points — Part 2: Video
This document defines various code points and fields that establish properties of a video (or still image) representation and are independent of the compression encoding and bit rate. These properties can describe the appropriate interpretation of decoded data or can, similarly, describe the characteristics of such a signal before the signal is compressed by an encoder that is suitable for…
Évaluation biologique des dispositifs médicaux — Partie 7: Résidus de stérilisation à l'oxyde d...
L'ISO 10993-7:2007 spécifie les limites admissibles des résidus d'oxyde d'éthylène (OE) et de chlorhydrate d'éthylène (ECH) pour des dispositifs médicaux individuels stérilisés à l'oxyde d'éthylène, les modes opératoires pour le mesurage de l'oxyde d'éthylène et du chlorhydrate d'éthylène et les méthodes de mesure en vue de déterminer leur conformité…
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…
