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This part of ISO/IEC 2382 is intended to facilitate international communication in artificial intelligence. It presents , in two languages, terms and definitions of selected concepts relevant to the field of information...

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

Scope This part of ISO/IEC 14443 specifies a half-duplex block transmission protocol featuring the special needs of a contactless environment and defines the activation and deactivation sequence of the protocol. This part of...

This part of ISO/IEC 19762 provides terms and definitions unique to radio frequency identification (RFID) in the area of automatic identification and data capture techniques. This glossary of terms enables the communication...

This part of ISO/IEC 19762 provides terms and definitions unique to optically readable media (ORM) in the area of automatic identification and data capture techniques. This glossary of terms enables the communication between...

This part of ISO/IEC 19762 provides general terms and definitions in the area of automatic identification and data capture techniques on which are based further specialized sections in various technical fields, as well as the...

This document specifies the particular requirements, including performance criteria for washer-disinfectors (WD) that are intended to be used for cleaning and chemical disinfection of thermolabile endoscopes. This document...

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...