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医用诊断用磁共振设备检测

发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22

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工业诊断 动物实验 植物学检测 环境试验

BS EN 60601-2-33:2010+A11:2011 电气.基本安全性和必要性能的详细要求

Medical electrical equipment. Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

BS EN 60601-2-33:2010 电气.的基本安全性和必要性能的详细要求

Replacement: This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MR EQUIPMENT and MR SYSTEMS, hereafter referred

Medical electrical equipment. Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

YY 0319-2000 电气.第2部分:安全专要求

本标准适用于2.2.101定义的磁共振设备。 本标准不包括用于医学研究的磁共振设备

Medical electrical equipment.Part 2:Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

KS C 9708-2022 显象剂

Phantoms for magnetic resonance equipment for medical diagnosis

JIS Z 4924:1995 人体模型

この規格は,診断用磁気共鳴装置の日常点検に用いるファントム(以下,ファントムという。)について規定する

Phantoms for magnetic resonance equipment for medical diagnosis

JIS Z 4924:2016 人体模型

Phantoms for magnetic resonance equipment for medical diagnosis

YY 0319-2008 电气.第2-33部分: 安全专要求

本专用标准适用于由2.2.101定义的磁共振设备和由2.2.102定义的磁共振系统。 本标准不涵盖磁共振设备预期用途之外的应用

Medical Electrical Equipment.Part 2-33:Particular Requirements for the Safety of Magnetic Reconance Equipment for Medical Diagnosis

GOST R 50267.33-1999 疗电气 第2部分安全专要求

Medical electrical equipment. Part 2. Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

NF C74-122/A1:2006 电气.第2-33部分:安全专要求

Medical electrical equipment - Part 2-33 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.

DIN EN 60601-2-33:2008 电气.第2-33部分:的安全特殊要求

Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2002 + A1:2005 + A2:2007); German version EN 60601-2-33:2002 + A1:2005 + A2:2008

IEC 60601-2-33:2010/AMD1:2013 电气.第2-33部分:的安全专要求

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

IEC 60601-2-33:2006 电气.第2-33部分:的安全专要求

This Particular Standard applies to MR EQUIPMENT as defined in 2.2.101 and MR SYSTEMS as defined in 2.2.102. This Standard does not cover

Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

NF C74-122:1996 电气.第2部分:的安全特殊要求

Medical electrical equipment. Part 2 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.

IEC 60601-2-33/AMD1:2006 电气.第2-33部分:的安全专要求.修改件1

Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient. Establishes requirements to provide

Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis; Amendment 1

SN/T 1672.6-2013 进出口检验规程 第X部分:

SN/T 1672的本部分规定了进出口医疗诊断用磁共振设备的检验要求。本部分适用于进出口医疗诊断用磁共振设备的进出口抽样、检验及判定

Rules for the inspection of import and export medical equipment.Part 6:Magnetic resonance imaging equipment for medical diagnosis

BS EN 60601-2-33:2010+A11:2011 电气.基本安全性和必要性能的详细要求

Medical electrical equipment. Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

BS EN 60601-2-33:2010 电气.的基本安全性和必要性能的详细要求

Replacement: This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MR EQUIPMENT and MR SYSTEMS, hereafter referred

Medical electrical equipment. Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

YY 0319-2000 电气.第2部分:安全专要求

本标准适用于2.2.101定义的磁共振设备。 本标准不包括用于医学研究的磁共振设备

Medical electrical equipment.Part 2:Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

KS C 9708-2022 显象剂

Phantoms for magnetic resonance equipment for medical diagnosis

JIS Z 4924:1995 人体模型

この規格は,診断用磁気共鳴装置の日常点検に用いるファントム(以下,ファントムという。)について規定する

Phantoms for magnetic resonance equipment for medical diagnosis

JIS Z 4924:2016 人体模型

Phantoms for magnetic resonance equipment for medical diagnosis

YY 0319-2008 电气.第2-33部分: 安全专要求

本专用标准适用于由2.2.101定义的磁共振设备和由2.2.102定义的磁共振系统。 本标准不涵盖磁共振设备预期用途之外的应用

Medical Electrical Equipment.Part 2-33:Particular Requirements for the Safety of Magnetic Reconance Equipment for Medical Diagnosis

GOST R 50267.33-1999 疗电气 第2部分安全专要求

Medical electrical equipment. Part 2. Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

NF C74-122/A1:2006 电气.第2-33部分:安全专要求

Medical electrical equipment - Part 2-33 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.

DIN EN 60601-2-33:2008 电气.第2-33部分:的安全特殊要求

Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2002 + A1:2005 + A2:2007); German version EN 60601-2-33:2002 + A1:2005 + A2:2008

IEC 60601-2-33:2010/AMD1:2013 电气.第2-33部分:的安全专要求

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

IEC 60601-2-33:2006 电气.第2-33部分:的安全专要求

This Particular Standard applies to MR EQUIPMENT as defined in 2.2.101 and MR SYSTEMS as defined in 2.2.102. This Standard does not cover

Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

NF C74-122:1996 电气.第2部分:的安全特殊要求

Medical electrical equipment. Part 2 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.

IEC 60601-2-33/AMD1:2006 电气.第2-33部分:的安全专要求.修改件1

Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient. Establishes requirements to provide

Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis; Amendment 1

SN/T 1672.6-2013 进出口检验规程 第X部分:

SN/T 1672的本部分规定了进出口医疗诊断用磁共振设备的检验要求。本部分适用于进出口医疗诊断用磁共振设备的进出口抽样、检验及判定

Rules for the inspection of import and export medical equipment.Part 6:Magnetic resonance imaging equipment for medical diagnosis

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