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DIN EN 60601-2-33:2017-11 WITHDRAWN

VDE 0750-2-33. Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis.
(VDE 0750-2-33. Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Magnetresonanzgeräten für die medizinische Diagnostik.)

WITHDRAWN published on 1.11.2017

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E DIN EN IEC 60601-2-33:2022-09 WITHDRAWN

VDE 0750-2-33. Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis.
(VDE 0750-2-33. Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Magnetresonanzgeräten für die medizinische Diagnostik.)

WITHDRAWN published on 1.9.2022

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E DIN EN 60601-2-33/A1:2004-08 WITHDRAWN

VDE 0750-2-33/A1. Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
(VDE 0750-2-33/A1. Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit von Magnetresonanzgeräten für die medizinische Diagnostik.)

WITHDRAWN published on 1.8.2004

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E DIN EN 60601-2-33/A1:2012-08 WITHDRAWN

VDE 0750-2-33/A1. Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis.
(VDE 0750-2-33/A1. Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit von Magnetresonanzgeräten für die medizinische Diagnostik.)

WITHDRAWN published on 1.8.2012

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E DIN EN 60601-2-33/A11:1997-03 WITHDRAWN

VDE 0750-2-33/A11. Medical electrical equipment - Part 2: Particular requirements for safety of magnetic resonance equipment for medical diagnosis.
(VDE 0750-2-33/A11. Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von medizinischen diagnostischen Magnetresonanzgeräten.)

WITHDRAWN published on 1.3.1997

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DIN EN 60601-2-33/A11:1998-02 WITHDRAWN

VDE 0750-2-33/A11. Medical electrical equipment - Part 2: Particular requirements for safety of magnetic resonance equipment for medical diagnosis; Amendment A11.
(VDE 0750-2-33/A11. Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von medizinischen diagnostischen Magnetresonanzgeräten; Änderung A11.)

WITHDRAWN published on 1.2.1998

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E DIN EN 60601-2-33/A2:2006-11 WITHDRAWN

VDE 0750-2-33/A2. Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
(VDE 0750-2-33/A2. Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit von Magnetresonanzgeräten für die medizinische Diagnostik.)

WITHDRAWN published on 1.11.2006

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E DIN EN 60601-2-33/A2:2016-05 WITHDRAWN

VDE 0750-2-33/A2. Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis.
(VDE 0750-2-33/A2. Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Magnetresonanzgeräten für die medizinische Diagnostik.)

WITHDRAWN published on 1.5.2016

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DIN EN 60601-2-33/Ber1:2009-05 WITHDRAWN

VDE 0750-2-33/Ber.1. Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
(VDE 0750-2-33/Ber.1. Medizinische elektrische Geräte - Teil 2-33: Besondere Festlegungen für die Sicherheit von Magnetresonanzgeräten für die medizinische Diagnostik.)

WITHDRAWN published on 1.5.2009

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E DIN EN 60601-2-34:1994-11 WITHDRAWN

VDE 0750-2-34. Medical electrical equipment - Part 2: Particular requirements for the safety of direct blood pressure monitoring equipment.
(VDE 0750-2-34. Medizinische elektrische Geräte - Teil 2: Besondere Festlegungen für die Sicherheit von invasiven Blutdruck-Überwachungsgeräten.)

WITHDRAWN published on 1.11.1994

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