11.040.55 诊断设备 标准查询与下载

DS/EN 61685:2002 超声波 流量测量系统 流量测试对象

This International Standard specifies parameters for a flow Doppler test object representing a blood vessel of known diameter at a certain depth in human tissue, carrying a steady flow. This International Standard establishes a flow Doppler test object which can be used to assess various aspects of the performance of Doppler diagnostics equipment.

Ultrasonics - Flow measurement systems - Flow test object

BS ISO 8600-2:2002 光学和光学仪器.医疗内诊镜和内诊镜附件.对刚性支气管镜的特殊要求

This part of ISO 8600 specifies definitions and requirements for rigid bronchoscopes and their endoscopic accessories used in the practice of anaesthesia and medical endoscopy.

Optics and optical instruments - Medical endoscopes and endoscopic accessories - Particular requirements for rigid bronchoscopes

ISO 8600-2:2002 光学和光学仪器.医疗内窥镜和内窥镜附件.第2部分:硬支气管内窥镜的特殊要求

This part of ISO 8600 specifies definitions and requirements for rigid bronchoscopes and their endoscopic accessories used in the practice of anaesthesia and medical endoscopy.

Optics and optical instruments - Medical endoscopes and endoscopic accessories - Part 2: Particular requirements for rigid bronchoscopes

LST EN 60601-2-34-2002 医疗电气设备 第 2-34 部分：有创血压监测设备（IEC 60601-2-34:2000）安全性的特殊要求，包括基本性能

Medical electrical equipment. Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment (IEC 60601-2-34:2000)

KS C IEC 60601-2-23:2002 医疗电气设备.第2-23部分:经皮氧分压监测仪

KS C IEC 60601-1의 1.1에 따르는 외에 다음 사항을 추가한다.이 규격은

Medical electrical equipment－Part 2－23： Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment

BS EN 60601-2-37:2001 医用电气设备.第2-37部分:超声波医疗诊断和监测设备的特殊安全要求

This Particular Standard specifies particular safety requirements for ULTRASONIC DIAGNOSTIC EQUIPMENT as defined in 2.1.145. This standard does not cover ultrasonic therapeutic equipment; however, equipment used for the imaging of body structures by ultrasound in conjunction with therapeutic modalities is covered.

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

ASTM E2065-02 心理生理检测欺骗（PDD）考官伦理要求标准指南

1.1 The purpose of this guide is to establish ethical requirements for all individuals engaged in forensic psychophysiological detection of deception (PDD).1.2 All individuals engaged in the practice of conducting PDD examinations shall adhere to this guide.

Standard Guide for Ethical Requirements for Psychophysiological Detection of Deception (PDD) Examiners

CAN/CSA-C22.2 No.60601-2-23-2002(R2011) 医用电气设备 第2-23部分：经皮分压监测设备的安全（包括基本性能）的特殊要求

This National Standard of Canada is equivalent to International Standard IEC 60601-2-23:1999, (second edition, 1999-12). 1 Scope and object This clause of the General Standard applies except as follows: *1.1 Scope Addition: This Particular Standard specifies requirements for the safety, including essential performance, of TRANSCUTANEOUS PARTIAL PRESSURE MONITORING EQUIPMENT, as defined in 2.101 and hereinafter referred to as EQUIPMENT, whether this EQUIPMENT is stand alone or part of a system. It applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth. It does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa). 1.2 Object Replacement: The object of this Particular Standard is to establish particular requirements for the safety, including essential performance, of TRANSCUTANEOUS PARTIAL PRESSURE MONITORING EQUIPMENT as defined in 2.101.

Medical Electrical Equipment - Part 2-23: Particular Requirements for the Safety, Including Essential Performance, of Transcutaneous Partial Pressure Monitoring Equipment

DS/EN 60601-2-49:2002 医用电气设备 第 2-49 部分：多功能病人监护设备安全的特殊要求

This standard applies to the safety requirements of MULTIFUNCTION PATIENT MONITORING EQUIPMENT as defined in sub-clause 2.2.101. The scope of this document is resticted to EQUIPMENT having either more than one APPLIED PART or having more than one SINGLE FUNCTION, intended for connection to a single PATIENT.

Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment

IEC 60601-2-33:2002 医用电气设备.第2-33部分:医疗诊断用磁共振设备安全的特殊要求

Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient. Establishes requirements to provide information to the operator, staff associated with magnetic resonance equipment and the general public. Pro

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

KS P IEC 60601-2-33:2002 磁共振计算机断层扫描装置

Magnetic resonance equipment for medical diagnosis

KS P IEC 60601-2-33-2002 磁共振计算机断层扫描装置

Magnetic resonance equipment for medical diagnosis

CAN/CSA-C22.2 No.60601-2-34-2002(R2011) 医用电气设备 第2-34部分：有创血压监测设备的安全（包括基本性能）的特殊要求

This National Standard of Canada is equivalent to International Standard IEC 60601-2-34:2000, (second edition, 2000-10). Scope and object This clause of the General Standard applies except as follows: * 1.1 Scope Addition: This Particular Standard applies to INVASIVE BLOOD PRESSURE MONITORING and measuring EQUIPMENT as defined in 2.101, hereinafter referred to as EQUIPMENT. This Particular Standard does not apply to catheter tubing, catherter needles, Luer locks, taps and tap tables. This Particular Standard also does not apply to NON-INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT. 1.2 Object Replacement: The object of this Particular Standard is to establish particular requirements for the safety, including the essential performance of EQUIPMENT, as defined in 2.101.

Medical Electrical Equipment - Part 2-34: Particular Requirements for the Safety, Including Essential Performance, of Invasive Blood Pressure Monitoring Equipment

CAN/CSA-C22.2 No.60601-2-34-2002(C2011) 医疗电气设备 第2-34部分：直接血压监测设备的特殊安全和基本性能要求

La présente norme nationale du Canada est équivalente a la norme internationale CEI/IEC 60601-2-34:2005. 1 Domaine d'application et objet L'article correspondant de la Norme Générale s'applique avec les exceptions suivantes: *1.1 Domaine d'application Addition: La présente Norme Particulière s'applique aux APPAREILS DE SURVEILLANCE et de mesure DE LA PRESSION SANGUINE PRÉLEVÉE DIRECTEMENT définis en 2.101 et appelés APPAREILS dans la présente norme. La présente Norme Particulière ne s'applique pas aux tubes et aiguilles de CATHÉTER, aux connecteurs Luer, aux prises et panneaux de prises, etc. La présente Norme Particulière ne s'applique pas non plus aux APPAREILS DE SURVEILLANCE DE LA PRESSION SANGUINE PRÉLEVÉE INDIRECTEMENT. 1.2 Objet Remplacement: L'objet de la présente Norme Particulière est d'établir des règles particulières de sécurité, y compris des exigences de performances essentielles pour les APPAREILS définis en 2.101.

Medical electrical devices - Part 2-34: Particular safety and essential performance requirements for direct blood pressure monitoring devices

CKS 352-2002 非自动血压计，无液气压计和水银

This specification covers requirements for aneroid and mercury type non-automated sphygmomano- meters to be used with occluding cuffs for the indirect measurement of arterial blood pressure. Requirements for occluding cuff, inflatable bladder, inflation device, connecting tubing and fastener are also covered.

Non-automated sphygmomanometers, aneroid and mercury

GOST 30324.30-2002 医疗电气设备.第2部分.自动循环间接血压监护仪的安全性详细要求

Medical electrical equipment. Part 2. Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment

SNI 16-6639-2002 激光诊断和治疗. 安全要求

Diagnostic and therapeutic laser equipment - Safety requirements

ASTM F2196-02 循环液体和加压气体的病人温度管理设施的标准规范

Addition:The object of this Particular Standard is to establish requirements for PATIENT TEMPERATURE MANAGEMENT DEVICES, which minimize hazards to PATIENT and OPERATOR and to specify tests by which compliance can be verified.

Standard Specification for Circulating Liquid and Forced Air Patient Temperature Management Devices

AS/NZS 4966:2002 给水用1/2 In.(12 mm)到2 In.(50 mm)聚乙烯-铝-聚乙烯和交联聚乙烯-铝-交联聚乙烯复合压力管

Describes test methods for measuring the performance of pulsed Doppler ultrasound systems, and applies to tests made on overall pulsed Doppler ultrasound system which is not disassembled or disconnected, and to tests made on pulsed Doppler ultrasound systems whether they are stand-alone or as part of another ultrasound instrument. Electrical safety, acoustic output and electromagnetic compatibility (EMC) are not covered in this technical specification. It is identical with and reproduced from IEC TS 61895:1999.

Ultrasonics - Pulsed Doppler diagnostic systems - Test procedures to determine performance

AS ISO 7376.1:2002 给水用1/2 In.(12 mm)到2 In.(50 mm)聚乙烯-铝-聚乙烯和交联聚乙烯-铝-交联聚乙烯复合压力管

Specifies requirements for laryngoscopes and critical dimensions for the junction of any handle and any blade of a hook-on type laryngoscope to allow engagement, lamp illumination and disengagement through multiple cycles.

Laryngoscopic fittings - Conventional hook-on type handle blade fittings