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This part of ISO/IEC 18000 defines the air interface for radio frequency identification (RFID) devices operating as an active RF tag in the 433 MHz band used in item management applications. It provides a common technical specification for RFID devices that can be used by ISO technical committees developing RFID application standards. This part of ISO/IEC 18000 is intended to allow for…

1.1 General This Document provides guidance in the evaluation of new materials and technologies in the physical environment. It is intended to help reduce health-care acquired infections (HAIs) and addresses the following topics: a) potential risks to patients, staff, and the environment; b) physical impacts; and c) human factors. 1.2 Intended users This Document is intended to be used by…

IEC 60601-1-12:2014 constitutes a collateral standard to IEC 60601-1: Medical electrical equipment - Part 1: General requirements for basic safety and essential performance hereafter referred to as the general standard. Medical practice is increasingly using medical electrical equipment and medical electrical systems for monitoring, treatment or diagnosis of patients in the emergency medical…

This is the first edition of CAN/CSA-IEC 62366-1, Medical devices — Part 1: Application of usability engineering to medical devices, which is an adoption without modification of the identically titled IEC (International Electrotechnical Commission) Standard 62366-1 (first edition, 2015-02). It replaces CAN/CSA-IEC 62366:14 (adopted IEC 62366:2007). For brevity, this Standard will be referred…

This is the fourth edition of CAN/CSA-Z8836, Suction catheters for use in the respiratory tract, which is an adoption, with Canadian deviations, of the identically titled ISO (International Organization for Standardization) Standard 8836 (fourth edition, 2014-10-15). It supersedes the previous edition published in 2011 as CAN/CSA-Z8836 (adopted ISO 8836:2007). For brevity, this Standard will…

This is the first edition of CAN/CSA-Z17510, Medical devices — Sleep apnoea breathing therapy — Masks and application accessories, which is an adoption, with Canadian deviations, of the identically titled ISO (International Organization for Standardization) Standard 17510 (first edition, 2015-08-01). It replaces CAN/CSA-Z17510-2-10 (adopted ISO 17510-2:2007). For brevity, this Standard will be…

This International Standard specifies minimum requirements for concentrates used for haemodialysis and related therapies. For the purpose of this International Standard, “concentrates” are a mixture of chemicals and water, or chemicals in the form of dry powder or other highly concentrated media, that are delivered to the end user to make dialysis fluid used to perform haemodialysis and…

ISO/IEC 18000-3:2015 defines the air interface for radio frequency identification (RFID) devices operating in the 860 MHz to 960 MHz Industrial, Scientific, and Medical (ISM) band used in item management applications. It provides a common technical specification for RFID devices that can be used by ISO committees developing RFID application standards. This part of ISO/IEC 18000 is intended to…

ISO/IEC 18000-3:2015 defines the air interface for radio frequency identification (RFID) devices operating in the 860 MHz to 960 MHz Industrial, Scientific, and Medical (ISM) band used in item management applications. It provides a common technical specification for RFID devices that can be used by ISO committees developing RFID application standards. This part of ISO/IEC 18000 is intended to…

ISO 24014-1:2015 provides the basis for the development of multi-operator/multi-service Interoperable public surface (including subways) transport Fare Management Systems (IFMSs) on a national and international level. ISO 24014-1:2015 is applicable to bodies in public transport and related services which agree that their systems need to interoperate. While ISO 24014-1:2015 does not imply that…