共找到 858 条与 诊断设备 相关的标准,共 58 页
Non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers
Non-invasive sphygmomanometers - Part 4 : test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers.
This European Standard describes test procedures for investigations to determine the overall system accuracy of automated non-invasive sphygmomanometers, designed for the indirect measurement of blood pressure.#,,#
Non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers; German version EN 1060-4:2004
This standard specifies requirements and recommended test methods for measuring the field of view and direction of view of endoscopes.
Optics and optical instruments - Medical endoscopes and endoscopic accessories - Part 3: Determination of field of view and direction of view of endoscopes with optics (ISO 8600-3:1997 + AMD 1:2003)
This document describes test procedures for investigations to determine the overall system accuracy of automated non-invasive sphygmomanometers, designed for the indirect measurement of blood pressure.
Non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers
This document describes test procedures for investigations to determine the overall system accuracy of automated non-invasive sphygmomanometers, designed for the indirect measurement of blood pressure.
Non-invasive sphygmomanometers - Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers
This National Standard of Canada is equivalent to International Standard IEC 60601-2-33:2002. 1 Scope and object This clause of the General Standard applies except as follows: 1.1 Scope Addition: This Particular Standard applies to MAGNETIC RESONANCE EQUIPMENT as defined in 2.2.101 and MAGNETIC RESONANCE SYSTEMS as defined in 2.2.102. This Standard does not cover the application of MAGNETIC RESONANCE EQUIPMENT beyond the INTENDED USE.
Medical Electrical Equipment - Part 2-33: Particular Requirements for the Safety of Magnetic Resonance Equipment for Medical Diagnosis
This National Standard of Canada is equivalent to International Standard IEC 60601-2-51:2003. 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 RECORDING AND ANALYSING SINGLE CHANNEL AND MULTICHANNEL ELECTROCARDIOGRAPHS as defined in 2.101, 2.111, 2.117, 2.123, 2.126, hereinafter referred to as EQUIPMENT. The EQUIPMENT may be attended or unattended. This Particular Standard complements IEC 60601-2-25 and its Amendment 1 (1999).
Medical Electrical Equipment - Part 2-51: Particular Requirements for Safety, Including Essential Performance, of Recording and Analysing Single Channel and Multichannel Electrocardiographs
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)
Medical electrical equipment. Part 2-51: Particular requirements for safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs (IEC 60601-2-51:2003)
本标准规定了医疗诊断用磁共振设备的术语、产品分类、技术要求和试验方法。 本标准适用于医疗诊断用磁共振设备。
Technical requirements and test methods for magnetic resonance equipment for medical diagnosis
This Particular Standard specifies the particular safety requirements for Electroencepthalographs as defined in 2.2. 103 and also referred to as equipment. This special requirements for other equipment also used in electroencephalography are not covered by this standard, for example: - cerebral fuction monitors; - phono-photic stimulators; - electronencephalograpic telemetry; - EEG data storage and retrieval; - Equipment particular intended for monitoring during electro-convulsive theraphy; - ambulatory electrocephalograhic recorders.
Medical electrical equipment - Part 2-26: Particular requirements for the safety of electroencephalographs
This Particular Standard specifies requirements for the safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs as defined in 2.101, 2.111, 2.117, 2.123, 2.126, hereinafter referred to as equipment. The equipment may be attended or unattended. This Particular Standard complements IEC 60601-2-25 and its Amendment 1 of 1999.
Medical electrical equipment - Part 2-51: Particular requirements for the safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs
This collateral standard specifies requirements for ALARM SYSTEMS and ALARM SIGNALS in MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS. It also provides guidance for the application of ALARM SYSTEMS.
Medical electrical equipment. General requirements for safety. Collateral standard. General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
Medical electrical equipment - Part 2-51: Particular requirements for safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs (IEC 60601-2-51:2003); German version EN 60601-2-51:2003
Medical electrical equipment - Part 2-26: Particular requirements for the safety of electroencephalographs (IEC 60601-2-26:2002); German version EN 60601-2-26:2003
Medical electrical equipment. Part 2. Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems
Medical electrical equipment. Part 2. Particular requirements for the safety of multifunction patient monitoring equipment
Safety requirements for electrical equipment for measurement, control, and laboratory use. Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment (IEC 61010-2-101:2002, modified)
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