共找到 858 条与 诊断设备 相关的标准,共 58 页
Ultrasonics - Field characterization - Test methods for the determination of thermal and mechanical indices related to medical diagnostic ultrasonic fields.
Medical electrical equipment - Part 2-18 : particular requirements for the safety of endoscopic equipment.
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 the application of MR EQUIPMENT beyond the INTENDED USE.
Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
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; Amendment 1
Ultrasonics. Field characterization. Test methods for the determination of thermal and mechanical indices related to medical diagnostic ultrasonic fields
This International Standard is applicable to medical diagnostic ultrasound fields. This standard establishes – parameters related to thermal and non-thermal aspects of diagnostic ultrasonic fields; – methods for the determination of an exposure parameter relating to temperature rise in theoretical tissue-equivalent models, resulting from absorption of ultrasound; – methods for the determination of an exposure parameter appropriate to certain nonthermal effects. NOTE In this standard where multiples or submultiples of SI units are used this is clearly stated and the usage is self-consistent.
Ultrasonics - Field characterization - Test methods for the determination of thermal and mechanical indices related to medical diagnostic ultrasonic fields
This Particular Standard applies to the safety requirements of MULTIFUNCTION PATIENT MONITORING EQUIPMENT as defined in subclause 2.2.101. The scope of this standard is restricted to EQUIPMENT having either more than one APPLIED PART or more than one SINGLE FUNCTION, intended for connection to a single PATIENT. This standard does not specify requirements for individual monitoring functions.
Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment
本标准规定了无菌、一次性使用的动脉管路血液过滤器(以下简称过滤器)的要求,该器件拟用于进行心肺转流手术时,滤除人体血液中的微栓、碎屑、血块、微气泡及其他具有潜在性危险的固体物质。
Cardiovascular implants and artificial organs-Cardiopulmonary bypass systems-Arterial line blood filters
Establishes particular requirements, in addition to the requirements of IEC 60601-2-25, for the safety, including essential performance of recording and analysing single channel and multichannel electrocardiographs. These requirements shall apply particu
Medical electrical equipment - Part 2-51: Particular requirements for the safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs
Medical electrical equipment - Part 2-25 : particular requirements for the safety of electrocardiographs.
Medical electrical equipment - Part 1-8 : 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 2-47 : Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems.
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 2-34 : particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment.
Medical electrical equipment - Part 2-49 : particular requirements for the safety of multifunction patient monitoring equipment
Medical electrical equipment - Part 2-51 : particular requirements for safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs.
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, CATHETER needles, Luer locks, taps and tap tables. This Particular Standard also does not apply to NON-INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT.
Medical electrical equipment - Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment
SN/T 1672 的本部分规定了对进出口经颅多普勒血液分析仪的抽样、检验及合格判定。 本部分适用于由电网电源或电源设备供电的经颅多普勒血液分析仪的进出口检验。
Rules for the inspection of medical equipment for import and export --Part 3: Transcranical Doppler blood flow analyzer
Medical electrical equipment - Part 2-37 : particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment.
Medical electrical equipment - Part 2-33 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
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