11.040.55 诊断设备 标准查询与下载
共找到 858 条与 诊断设备 相关的标准，共 58 页
IEC 62563-1:2009 describes the evaluation methods for testing medical image display systems. It is directed to practical tests that can be visually evaluated or measured using basic test equipment. More advanced or more quantitative measurements can be performed on these devices, but these are beyond the scope of this document. IEC 62563-1:2009 applies to medical image display systems, which can display monochrome image information in the form of greyscale values on colour and greyscale image display systems (e.g. cathode ray tube (CRT) monitors, flat panel displays, projection system). This standard applies to medical image display systems used for diagnostic (interpretation of medical images toward rendering clinical diagnosis) or viewing (viewing medical images for medical purposes other than for providing a medical interpretation) purposes and therefore having specific requirements in terms of image quality. Head mounted image display systems and image display systems used for confirming positioning and for operation of the system are not covered by this standard.
Medical electrical equipment - Medical image display systems - Part 1: Evaluation methods
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- 11.040.55
- CCS
- 发布
- 2010-03-05
- 实施
- 2010-06-01 (7)
Non-invasive sphygmomanometers - Part 1 : general requirements.
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- 11.040.55
- CCS
- C39
- 发布
- 2010-03-01
- 实施
Non-invasive sphygmomanometers - Part 1 : general requirements.
- ICS
- 11.040.55
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- C39
- 发布
- 2010-03-01
- 实施
- 2010-03-10
The document, in conjunction with EN 1060-1:1994 and EN 1060-1 A1:2009, specifies performance, efficiency and mechanical and electrical safety requirements, including test methods, for non-invasive mechanical sphygmomanometers and their accessories which, by means of an inflatable cuff, are used for the non-invasive measurement of arterial blood pressure.
Non-invasive sphygmomanometers - Part 2: Supplementary requirements for mechanical sphygmomanometers; German version EN 1060-2:1995+A1:2009
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- 11.040.55
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- C38
- 发布
- 2010-03
- 实施
- 2010-03-01
This Technical Specification spezifies and describs the general concepts of the limits of applicability of acoustic measurements in water, a method to ensure that measurements are made under quasi-linear conditions, to acoustic fields in the frequency range 0.5 MHz to 15 MHz to both circular and rectangular source geometries and both contiuous-wave and pulsed fields. It also spezifies the definition of an acoustic quantity appropriate for establishing quasi-linear conditions, a threshold value for the acoustic quantity as an upper limit for quasi-linear conditions and a method for the estimation of attenuated acoustic quantities under conditions of nonlinear propagation in water.
Ultrasonics - Field characterization - In situ exposure estimation in finite-amplitude ultrasonic beams (IEC/TS 61949:2007); German version CLC/TS 61949:2008
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- 11.040.55
- CCS
- C41
- 发布
- 2010-03
- 实施
- 2010-03-01
The document specifies performance and overall accuracy requirements for electro-mechanical blood pressure measuring systems. EN 1060-4 is specifies as test method for the overall accuracy
Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems; German version EN 1060-3:1997+A2:2009
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- 11.040.55
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- C38
- 发布
- 2010-03
- 实施
- 2010-03-01
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MR EQUIPMENT and MR SYSTEMS, hereafter referred to also as ME EQUIPMENT. This standard does not cover the application of MR EQUIPMENT beyond the INTENDED USE. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant. The standard does not formulate ESSENTIAL PERFORMANCE requirements related to INTERVENTIONAL MR EXAMINATIONS.
Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
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- 11.040.55
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- C39
- 发布
- 2010-03
- 实施
- 2010-03-12
Medical electrical equipment -- Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening (IEC 80601-2-59:2008 + corrigendum 2009)
- ICS
- 11.040.55
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- 发布
- 2010-02-26
- 实施
- 2010-02-26
This Part of EN 1060 specifies performance, efficiency and safety requirements for electro-mechanical blood pressure measuring systems that, by means of an inflatable cuff are used for non-invasive measurements of arterial blood pressure at the upper arm, the wrist and the thigh. It also specifies requirements for their accessories and gives test methods.This Part of EN 1060 applies to electro-mechanical blood pressure measuring systems in which the cuff pressure is measured electronically, but in which the blood pressure can be determined either manually with the aid of a stethoscope or automatically.Additional safety requirements for automatic cycling ind
Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems
- ICS
- 11.040.55
- CCS
- 发布
- 2010-01-29
- 实施
- 2010-01-29
Non-invasive sphygmomanometers - Part 3 : supplementary requirements for electro-mechanical blood pressure measuring systems.
- ICS
- 11.040.55
- CCS
- C38
- 发布
- 2010-01-01
- 实施
Non-invasive sphygmonanometers - Part 2 : supplementary requirements for mechanical sphygmomanometers.
- ICS
- 11.040.55
- CCS
- C39
- 发布
- 2010-01-01
- 实施
- 2010-01-16
Non-invasive sphygmomanometers - Part 3 : supplementary requirements for electro-mechanical blood pressure measuring systems.
- ICS
- 11.040.55
- CCS
- C39
- 发布
- 2010-01-01
- 实施
- 2010-01-16
Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening (First Edition; Incorporates Corrigendum 1: June 2011)
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- 11.040.55
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- 发布
- 2010-01-01
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1.1 This guide establishes essential and recommended elements in the procedures for the conduct of a psychophysiological detection of deception (PDD) examination. 1.1.1 Other unique PDD applications are addressed separately.
Standard Guide for PDD Examination Standards of Practice
- ICS
- 11.040.55
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- A92
- 发布
- 2010
- 实施
YY/T 0162的本部分规定了B型超声诊断设备档次划分的方法和各档次设备的性能指标及应具备的条件。 本部分适用于标称频率不超过15MHz范围内的B型超声诊断设备，作为此范围内B型超声诊断设备划分档次的参考依据。 本部分不适用于眼科专业超声诊断设备和血管内超声诊断设备。
Medical ultrasound equipment class series.Part 1:B mode ultrasound disgnostic equipment
- ICS
- 11.040.55
- CCS
- C41
- 发布
- 2009-11-15
- 实施
- 2010-12-01
This Part of EN 1060 specifies performance, efficiency and safety requirements for electro-mechanical blood pressure measuring systems that, by means of an inflatable cuff are used for non-invasive measurements of arterial blood pressure at the upper arm, the wrist and the thigh. It also specifies requirements for their accessories and gives test methods. This Part of EN 1060 applies to electro-mechanical blood pressure measuring systems in which the cuff pressure is measured electronically, but in which the blood pressure can be determined either manually with the aid of a stethoscope or automatically. Additional safety requirements for automatic cycling indirect blood pressure monitoring equipment are specified in EN 60601-2-30:1995. This Part of EN 1060 is to be used in conjunction with EN 1060-1.
Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems
- ICS
- 11.040.55
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- C38
- 发布
- 2009-11
- 实施
Covers requirements for aneroid and mercury type non-automated sphygmomanometers to be used with occluding cuffs for the indirect measurement of arterial blood pressure. Requirements for occluding cuff, inflatable bladder, inflation device, connecting tu
Non-automated sphygmomanometers, aneroid and mercury
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- 11.040.55
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- C38
- 发布
- 2009-10-23
- 实施
Medical electrical equipment - Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement
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- 11.040.55
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- C38
- 发布
- 2009-10
- 实施
Medical electrical equipment - Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use (ISO 9919:2005); German version EN ISO 9919:2009
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- 11.040.55
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- C39
- 发布
- 2009-09
- 实施
- 2009-09-01
This Part of EN 12470 specifies performance requirements and test methods for clinical liquid-in-glass thermometers with maximum device and applies only to thermometers filled with metallic liquid.NOTE 1 Note that in some European countries the use of mercury is prohibited in clinical thermometers. NOTE 2 Substances other than metallic liquids can be used in the manufacturing of liquid-in-glass thermometers. No reference is made to these in this European standard because there is no experience of clinical thermometers which use other substances.This European Standard does not apply to clinical thermometers designed for special applications (e.g. thermometer
Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device
- ICS
- 11.040.55
- CCS
- 发布
- 2009-08-05
- 实施
- 2009-08-05
