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ISO 22745 Industrial automation systems and integration - Open technical dictionaries and their application to master data ISO 22745-2:2010 Part 2: Vocabulary; ISO/IEC TR 22767:2005 Information technology – Telecommunications and information exchange between systems – Using CSTA for SIP phone user agents (uaCSTA)
An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.
The process of using concept identifiers from an external open technical dictionary is a form of semantic encoding compliant with the requirements of ISO 8000-110:2008, the international standard for the exchange of quality master data. The eOTD concept identifiers are in the public domain.
Medical device connectivity is the establishment and maintenance of a connection through which data is transferred between a medical device, such as a patient monitor, and an information system. The term is used interchangeably with biomedical device connectivity or biomedical device integration.
The standard "ISO/IEEE International Standard for Health informatics - Point-of-care medical device communication - Part 20702: Medical devices communication profile for web services" [7] (short Medical DPWS or MDPWS) enables the foundational interoperability between medical devices. This includes the ability of medical devices to exchange data ...
Historically, most classes of technical documentation lacked universal conformity for format, content and structure. Standards are being developed to redress this through bodies such as the International Organization for Standardization(ISO), which has published standards relating to rules for preparation of user guides, manuals, product specifications, etc. for technical product documentation.
This article needs to be updated.The reason given is: the section related to E.U. needs further updates (esp. in sections 3.2 and 4.2.2) as the directives 93/42/EEC on medical devices and 90/385/EEC on active implantable medical devices have been fully repealed on 26 May 2021 by Regulation (EU) no. 2017/745 (MDR); furthermore, Brexit triggers updates in these sections (U.K. developed their own ...
Global Medical Device Nomenclature (GMDN) is a system of internationally agreed generic descriptors used to identify all medical device products. This nomenclature is a naming system for products which include those used for the diagnosis, prevention, monitoring, treatment or alleviation of disease or injury in humans.