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DIN 267-29: Fasteners – Part 29: Technical specifications; Product grades for parts for bolted connections for use at temperatures ranging from −200 °C to +700 °C: Withdrawn: DIN 267-30: Fasteners – Part 30: Technical specifications; Metric thread rolling screws of property class 10.9: Active: DIN 276-1: Building costs; Part 1: Building ...
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This is a list of published [note 1] standards and other deliverables of the International Organization for Standardization (ISO). [note 2] For a complete and up-to-date list of all the ISO standards, see the ISO catalogue. [1] The standards are protected by copyright and most of them must be purchased.
The figure below (based on one from the IEEE 11073-20601 standard) shows the IEEE 11073 Personal Health Device Domain Information Model, expressed as a UML class diagram. The MDS object (and the objects that it contains) belongs to the Agent, but the Manager is able to build its own representation by interrogating the Agent.
CEN ISO/IEEE 11073 Health informatics - Medical / health device communication standards enable communication between medical, health care and wellness devices and external computer systems. They provide automatic and detailed electronic data capture of client-related and vital signs information , and of device operational data.
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 15189 Medical laboratories — Requirements for quality and competence is an international standard that specifies the quality management system requirements particular to medical laboratories. The standard was developed by the International Organisation for Standardization 's Technical Committee 212 (ISO/TC 212).
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