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IEC 60601-2-68:2014 applies to the basic safety and essential performance of X-ray based image-guided radiotherapy (IGRT) equipment for use with External Beam Equipment (EBE). This particular standard covers safety aspects of kilovoltage and megavoltage X-ray imaging devices in a known geometrical relationship with EBE for the purpose of IGRT. IEC 60601-2-13:2003 Medical electrical equipment — Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems IEC 60601-2-52:2009/Amd 1:2015 Medical electrical equipment — Part 2-52: Particular requirements for the basic safety and essential performance of medical beds — Amendment 1 IEC 80601-2-59:2017 applies to the basic safety and essential performance of screening thermographs intended to be used for the individual non-invasive febrile temperature screening of a human under controlled environmental conditions, hereafter referred to as ME equipment. IEC 60601-1-2:2014 applies to the basic safety and essential performance of Medical Equipment (ME) equipment and ME systems in the presence of electromagnetic disturbances and to electromagnetic disturbances emitted by me equipment and me systems. IEC 60601-2-22:2019 applies to the Basic Safety and Essential Performance of laser equipment for surgical, therapeutic, medical diagnostic, cosmetic or veterinary applications, intended for use on humans or animals, classified as Laser Product of Class 1C where the Enclosed Laser is of Class 3B or 4, or Class 3B, or Class 4.

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• Uppfyller NHS ”National Patient Safety Agency”. (NPSA/2010/RRR019). Spruta lossnat, nästan slut- och slut av  230 VAC. 600 VA. 60 Hz. Standarder. Säkerhet. EMC. Vätskeskydd. IEC 606011, EN 606011, UL606011;.

In contrast, regulation supports the evaluation each component of a system as a seperate medical device. IEC 60601-2-39:2019 applies to the basic safety and essential performance of peritoneal dialysis medical electrical equipment.

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Denna standard beskriver specifika krav när det gäller elektrisk utrustning inom sjukvården, exempelvis grundläggande säkerhet och viktig  strömförsörjd enligt EN 60601-1. Konstruktionsstandarder: Fyller gällande krav i EN 60601-1,. EN 60601-1-11, IEC 60601-2-4. Miljö.

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IEC 60601-2-10 National Deviation Canada cl. 6.8.3 bb). The maximum output charge per pulse and maximum average current across a. 500 ohm resistive load  Applying three different methods of measuring CTDIfree air to the extended CTDI formalism for wide-beam scanners (IEC 60601-2-44): a comparative study  IEC 60601-2-38 och. ANSI/AAMI ES60601-1:2005. CAN/CSA C22.2 nr 60601-1:08.

IEC 60601-2-20:2020 is available as IEC 60601-2-20:2020 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition. IEC 60601-2-20:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT TRANSPORT INCUBATOR equipment, as defined in 201.3.208, also referred to as ME EQUIPMENT. IEC 60601-2-19:2020 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition. IEC 80601-2-59:2017 applies to the basic safety and essential performance of screening thermographs intended to be used for the individual non-invasive febrile temperature screening of a human under controlled environmental conditions, hereafter referred to as ME equipment. IEC 60601-2-22:2019 is available as IEC 60601-2-22:2019 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition. IEC 60601-2-22:2019 applies to the Basic Safety and Essential Performance of laser equipment for surgical, therapeutic, medical diagnostic, cosmetic or veterinary applications, intended for IEC 60601-2-21:2020 is available as IEC 60601-2-21:2020 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.
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IEC 60601-2-16:2018 includes all electromedical equipment that is intended to deliver a haemodialysis, haemodiafiltration and haemofiltration treatment to a patient suffering from kidney failure.

Överensstämmer med standarderna. IEC 60601-1, IEC 60601-1-2, IEC 60601-2-41. Egenskaperna i korthet.
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Elektrisk utrustning för medicinskt bruk  Standarden baserades på den internationella versionen IEC 60601-2-12. Inom ramen för VDE- standarderna klassificeras standarden som  TS EN IEC 60601-2-39 Elektriska medicintekniska produkter - Del 2-39: Grundläggande säkerhet för peritonealdialysenheter och specifika funktioner för  IEC 60601-2-18: Medicinsk elektrisk utrustning, del 2-18: Särskilda krav för grundläggande säkerhet och nödvändig prestanda hos endoskopisk utrustning. IEC 60601-2-19-standarden, utarbetad av International Electrotechnical Commission (IEC), ett dotterbolag till International Standards Organization (ISO), är en . Standard Svensk standard · SS-EN IEC 60601-2-39. Elektrisk utrustning för medicinskt bruk - Säkerhet och väsentliga prestanda - Del 2-39: Särskilda fordringar  2 kV för 1 mA/1 minut vid 50 Hz överensstämmer med EN/IEC 61812-1.