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在医院实施美国食品药品监督管理局关于电极导线和患者电缆的性能标准。

Implementing the FDA performance standard on electrode lead wires and patient cables in hospitals.

作者信息

Tsitlik J E, Rose D C, Baumann R C

机构信息

Clinical Engineering Department, Service-Master Management Services Company, Downers Grove, Illinois, USA.

出版信息

Biomed Instrum Technol. 2000 Jul-Aug;34(4):295-303.

Abstract

The U.S. Food and Drug Administration (FDA) Performance Standard on Electrode Lead Wires and Patient Cables became mandatory for all relevant devices on May 9, 2000. The standard requires that any lead wire or patient cable that has contact, temporary or permanent, with a patient, should not allow the connection of the patient to the earth or possibly hazardous voltages. This article advises those hospitals and other healthcare facilities that have not completed the upgrades of wires and cables on how to complete this task.

摘要

美国食品药品监督管理局(FDA)关于电极导线和患者电缆的性能标准于2000年5月9日对所有相关设备强制生效。该标准要求,任何与患者有临时或永久接触的导线或患者电缆,均不应使患者与大地或可能存在危险的电压相连。本文为尚未完成电线和电缆升级的医院及其他医疗保健机构提供如何完成此项任务的建议。

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