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Haulla "1010" löytyi 83 tulosta.

SFS-EN ISO 11073-10102:en – Health informatics. Point-of-care medical device communication. Part 10102: Nomenclature. Annotated ECG (ISO/IEEE 11073-10102:2014)

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ISO/IEEE 11073-10102:2014 extends the IEEE 11073-10101 Nomenclature by providing support for ECG annotation terminology. It may be used either in conjunction with other IEEE 11073 standards (e.g. ISO/IEEE 11073-10201:2001) or independently with other standards. The major subject areas addressed b ...
https://sales.sfs.fi/julkaisu.html.stx?id=247493

SFS-EN ISO 11073-10103:en – Health informatics. Point-of-care medical device communication. Part 10103: Nomenclature. Implantable device, cardiac (ISO/IEEE 11073-10103:2014, Corrected version 2014-05-01)

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ISO/IEEE 11073-10103:2014 extends the base nomenclature provided in IEEE 11073 to support terminology for implantable cardiac devices. Devices within the scope of this nomenclature are implantable devices such as pacemakers, defibrillators, devices for cardiac resynchronization therapy, and impla ...
https://sales.sfs.fi/julkaisu.html.stx?id=244063

SFS-EN ISO 11073-10101:2020:en – Health informatics. Device interoperability. Part 10101: Point-of-care medical device communication. Nomenclature (ISO/IEEE 11073-10101:2020)

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This document defines a nomenclature for communication of information from point-of-care medical devices. Primary emphasis is placed on acute care medical devices and patient vital signs information. The nomenclature also supports concepts in an object-oriented information model that is for medic ...
https://sales.sfs.fi/julkaisu.html.stx?id=931496

SFS-EN 61010-2-020:2017:en – Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 2-020: Particular requirements for laboratory centrifuges

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IEC 61010-2-020:2016 is available as IEC 61010-2-020:2016 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition. IEC 61010-2-020:2016 is applicable to electrically powered LABORATORY CENTRIFUGES. This ...
https://sales.sfs.fi/julkaisu.html.stx?id=492056

SFS-EN 61010-2-101:2017:en – Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment

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IEC 61010-2-101:2015 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety function, as specified in IEC Guide 104. This standard has been prepared in close collaboration with Working Group CENEL ...
https://sales.sfs.fi/julkaisu.html.stx?id=475910

SFS-EN IEC 61010-2-201:2018:en – Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 2-201: Particular requirements for control equipment

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NEW!IEC 61010-2-201:2017 is available as IEC 61010-2-201:2017 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.IEC 61010-2-201:2017 specifies safety requirements and related verification tests for ...
https://sales.sfs.fi/julkaisu.html.stx?id=682359

SFS-EN 61010-1:2011/A1:2019/AC:2019:en – Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 1: General requirements

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IEC 61010-1:2010 specifies general safety requirements for the following types of electrical equipment and their accessories, wherever they are intended to be used. a) Electrical test and measurement equipment b) Electrical industrial process-control equipment c) Electrical laboratory equipment ...
https://sales.sfs.fi/julkaisu.html.stx?id=765065
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