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specifies requirements and provides guidance on the enumeration and microbial characterization of the population of viable microorganisms on or in a health care product, component, raw material or package

specifies general performance requirements for washer-disinfectors (WD) and their accessories that are intended to be used for cleaning and disinfection of re-usable medical devices and other articles used in the context of...

specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices. It also specifies requirements and provides guidance in relation to depyrogenation processes...

ISO 10524-1:2018 specifies the design, construction, type testing, and marking requirements for pressure regulators intended for the administration of medical gases and their mixtures in the treatment, management, diagnostic...

ISO 10524-2:2018 specifies design, construction, type testing, and marking requirements for manifold pressure regulators and line pressure regulators intended for use in medical gas pipeline systems. Examples of gases include...

This document specifies design, type testing, and marking requirements for cylinder valves with integrated pressure regulators [as defined in 3.26 and referred to hereafter as valves with integrated pressure regulators (VIPRs...

ISO 9170-1:2017 is intended especially to ensure the gas-specific assembly, mechanical resistance, flow, leakage and pressure drop of terminal units and to prevent their interchange between different gases and services and...

This second edition cancels and replaces the first edition published in 2009 and amendment 1:2013. This new edition constitutes a technical revisions This edition includes the following significant technical changes with...

This part of ISO/IEC 10118 specifies dedicated hash-functions, i.e. specially designed hash-functions. The hash-functions in this part of ISO/IEC 10118 are based on the iterative use of a round-function. Seven distinct round...

ISO 10079-2:2014 specifies safety and performance requirements for medical, manually powered suction equipment intended for oro-pharyngeal suction. It covers equipment operated by foot or by hand or both. Annex C illustrates...

ISO 10079-3:2014 specifies safety and performance requirements for medical suction equipment powered from a vacuum or positive pressure gas source generating venturi suction. It applies to equipment connected to medical gas...

ISO 23328-1:2003 gives a short-term airborne sodium chloride particle challenge test method for assessing the filtration performance of breathing system filters (BSF) intended for the filtration of respired gases