EN 60601-2-33:2010/AC:2016-03
(Corrigendum)Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
General Information
- Abstract
IEC corrigendum
- Status
- Published
- Publication Date
- 03-Mar-2016
- Technical Committee
- CLC/TC 62 - Electrical equipment in medical practice
- Drafting Committee
- CLC/TC 62 - Electrical equipment in medical practice
- Current Stage
- 6060 - Document made available - Publishing
- Start Date
- 04-Mar-2016
- Completion Date
- 04-Mar-2016
- Directive
- Not Harmonized93/42/EEC - Medical devicesOJ Ref: C, C 389 OJ Date: 17-Nov-2017
Relations
- Effective Date
- 03-Aug-2020
- Effective Date
- 01-Mar-2016
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Frequently Asked Questions
EN 60601-2-33:2010/AC:2016-03 is a corrigendum published by CLC. Its full title is "Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis". This standard covers: IEC corrigendum
IEC corrigendum
EN 60601-2-33:2010/AC:2016-03 is classified under the following ICS (International Classification for Standards) categories: 11.040.55 - Diagnostic equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-33:2010/AC:2016-03 has the following relationships with other standards: It is inter standard links to EN IEC 60601-2-33:2024, EN 60601-2-33:2010. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-33:2010/AC:2016-03 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/295. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.
EN 60601-2-33:2010/AC:2016-03 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit von Magnetresonanzgeräten für die medizinische DiagnostikAppareils électromédicaux - Partie 2-33: Exigences particulières pour la sécurité de base et les performances essentielles des appareils à résonance magnétique utilisés pour le diagnostic médicalMedical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis11.040.55Diagnostic equipmentICS:Ta slovenski standard je istoveten z:EN 60601-2-33:2010/AC:2016-03SIST EN 60601-2-33:2010/AC:2016en01-maj-2016SIST EN 60601-2-33:2010/AC:2016SLOVENSKI
STANDARD
EUROPEAN STANDARD NORME EUROPÉENNE EUROPÄISCHE NORM EN 60601-2-33:2010/AC:2016-03
March 2016
ICS 11.040.55 English Version
Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2010/COR2:2016)
Appareils électromédicaux - Partie 2-33: Exigences particulières pour la sécurité de base et les performances essentielles des appareils à résonance magnétique utilisés pour le diagnostic médical (IEC 60601-2-33:2010/COR2:2016)
Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit von Magnetresonanzgeräten für die medizinische Diagnostik (IEC 60601-2-33:2010/COR2:2016) This corrigendum becomes effective on 4 March 2016 for incorporation in the Englis
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