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ISO 7010 is an International Organization for Standardization technical standard for graphical hazard symbols on hazard and safety signs, including those indicating emergency exits. It uses colours and principles set out in ISO 3864 for these symbols, and is intended to provide "safety information that relies as little as possible on the use of ...
English: ISO 15223-1 (Medical devices). Symbol for medical device labels, labelling and information to be supplied. Indicates a medical device that is intended for one use, or for use on a single patient during a single procedure.
ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.
ISO 27185:2012 Cardiac rhythm management devices - Symbols to be used with cardiac rhythm management device labels, and information to be supplied - General requirements; ISO 27186:2010 Active implantable medical devices – Four-pole connector system for implantable cardiac rhythm management devices – Dimensional and test requirements
This is a list of abbreviations used in medical prescriptions, including hospital orders (the patient-directed part of which is referred to as sig codes). This list does not include abbreviations for pharmaceuticals or drug name suffixes such as CD, CR, ER, XT (See Time release technology § List of abbreviations for those).
ISO/IEC 18328-2:2015 Part 2: Physical characteristics and test methods for cards with devices; ISO/IEC 18328-3:2016 Part 3: Organization, security and commands for interchange; ISO/TS 18339:2015 Endotherapy devices – Eyepiece cap and light guide connector
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as the directives 93/42/EEC on medical devices and 90/385/EEC on active implantable medical devices have been fully repealed on 26 May 2021 by Regulation (EU) no. 2017/745 (MDR); furthermore, Brexit triggers updates in these sections (U.K. developed their own ...
ISO 20916:2019 In vitro diagnostic medical devices -- Clinical performance studies using specimens from human subjects -- Good study practice; ISO/IEC 20919:2016 Information technology – Linear Tape File System (LTFS) Format Specification; ISO/IEC 20922:2016 Information technology – Message Queuing Telemetry Transport v3.1.1