11.040.55 诊断设备 标准查询与下载

DS/EN 12470-2+A1:2009 临床温度计 第2部分：相变型（点阵）温度计

This Part of EN 12470 specifies performance requirements and test methods for phase change-type (dot matrix) thermometers for measuring temperature in body cavities.NOTE A body cavity can be the mouth, rectum or armpit.This European Standard does not apply to clinical thermometers designed for special applications (e.g. thermometers for hypothermia) which owing to their measurement range, scale interval or maximum permissible error do not meet the requirements specified in this Standard.

Clinical thermometers - Part 2: Phase change type (dot matrix) thermometers

NF S97-150-3/IN1:2009 医用体温计.第3部分:最大装置小型电体温计(非预测型和预测型)的性能

Clinical thermometers - Part 3 : performance of compact electrical thermometers (non-predictive and predictive) with maximum device.

NF S97-150-4/IN1:2009 医用体温计.第4部分:连续测量用电体温计性能

Clinical thermometers - Part 4 : performance of electrical thermometers for continuous measurement.

SANS 373-2:2009 内窥镜再加工.第2部分:刚性内窥镜，相关的零件及附件

Provides a code of practice for the preparation of rigid endoscopes, associated components and the reusable endoscopic accessories used with rigid endoscopes, for reuse, using washer disinfectors, steam, or chemicals in the reprocessing environment. It c

Reprocessing of endoscopes Part 2: Rigid endoscopes, associated components and accessories

SANS 373-1:2009 内窥镜再加工.第1部分:灵活内窥镜及附件

Provides a code of practice for the preparation of flexible fiber-optic endoscopes, video endoscopes and the reusable endoscopic accessories used with flexible endoscopes, for reuse, either manually or using automatic endoscope reprocessors. It covers th

Reprocessing of endoscopes Part 1: Flexible endoscopes and accessories

ISO 81060-2:2009 非侵入性血压计.第2部分:自动测量式临床验证

Non-invasive sphygmomanometers - Part 2: Clinical validation of automated measurement type

ISO/TR 13154:2009 医疗电气设备.筛选温度计用鉴定发热人群用部署、实施和操作指南

Medical electrical equipment - Deployment, implementation and operational guidelines for indentifying febrile humans using a screening thermograph

DIN EN 61157 Berichtigung 1:2009 医疗诊断超声波设备声输出的报告用标准方法.技术勘误DIN EN 61157-2008-07

Standard means for the reporting of the acoustic output of medical diagnostic ultrasonic equipment (IEC 61157:2007); German version EN 61157:2007, Corrigendum to DIN EN 61157:2008-07

IEC 61676:2002+AMD1:2008 CSV 医用电气设备.放射诊断学中X射线管电压无创测量用剂量计

Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology

IEC 80601-2-30:2009 医疗电气设备.第2-30部分:自动非侵入式血压测量计的基本安全性和基本性能用详细要求

Inhaltsverzeichnis

Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers

ANSI/AAMI/IEC 80601-2-30/C1:2009 医疗电气设备.第2-30部分:自动非侵入式血压测量计的基本安全性和基本性能的详细要求

Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated type non-invasive sphygmomanometers

GOST R IEC 60601-2-33-2009 医疗电气装置.第2-33部分:医疗诊断磁共振设备安全的特定要求

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

GOST R 53466-2009 光学元件与设备.医用温度计.一般技术要求.主要参数的测量方法

Optics and optical equipment. Medical thermographs. General technical requirements. Methods of measuring the major parameters

ANSI/ASA S3.45-2009 基本前庭功能的试验程序

Defines test procedures, measurements, data analysis, and data reporting requirements for performing and reporting a battery of six different tests for the evaluation of human vestibular function ("Basic Vestibular Function Test Battery"). Stimuli are presented to evoke eye movement by a subject whose response is determined either by measurement of electrical signals generated by the eye movements or by image processing methods applied to video eye movements. Test interpretation is not included.

Procedures for Testing Basic Vestibular Function

ASTM E2229-09 欺骗性(复写器)数据精神心理学检测说明的标准实施规范

1.1 These practices establish procedures for the systematic interpretation and analysis of Psychophysiological Detection of Deception (PDD) data. 1.2 Any test data analysis procedure used shall be correctly matched to the PDD examination format. Examiners shall use evaluation methods for which they have been formally trained. 1.2.1 Acceptable test data analysis procedures are those published in refereed or technical journals, and for which published replications of the procedures have confirmed their efficacy.

Standard Practices for Interpretation of Psychophysiological Detection of Deception (Polygraph) Data

GOST R 53469-2009 光学和光学仪器.医用内窥镜与内疗器件.第1部分:一般要求

Optics and optical instruments. Medical endoscopes and endotherapy devices. Part 1. General requirements

ANSI/AAMI/IEC 80601-2-30:2009 医疗电气设备.第2-30部分:自动无创伤性血压计的基本安全性和必要性能的详细要求

This standard applies to the basic safety and essential performance of automated sphygmomanometers which are used for the non-invasive blood pressure measurement.

Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers

ANSI/AAMI/IEC 80601-2-30:2009/C1:2009 医疗电气设备.第2-30部分:自动无创伤性血压计的基本安全和性能的详细要求

Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated type non-invasive sphygmomanometers

CAN/CSA-C22.2 No.60601-2-37-2008(R2019) 医用电气设备 第2-37部分：超声医疗诊断和监护设备基本安全和基本性能的特殊要求

This National Standard of Canada is equivalent to International Standard IEC 60601-2-37:2007. Scope Addition: This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ULTRASONIC DIAGNOSTIC EQUIPMENT as defined in 201.3.217, hereinafter referred to as ME EQUIPMENT. 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. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of this standard. NOTE See also subclause 4.2 of this standard. This particular standard does not cover ultrasonic therapeutic equipment. Equipment used for the imaging or diagnosis of body structures by ultrasound in conjunction with other medical procedures is covered.

Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment

CAN/CSA-C22.2 NO.60601-2-37-2008 医用电气设备第2-37部分：超声医疗诊断和监护设备基本安全和基本性能的特殊要求（第二版）

Medical electrical equipment — Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment (Second Edition)