请注意:此版本的所有临时修订版将在您购买时提供。冷藏医疗设备UL 4161范围1。1这些要求包括根据《国家电气规范》在医院、养老院、医疗保健中心、医疗和牙科办公室以及类似医疗保健设施中使用的冷藏医疗设备，如热疗和氧疗设备，NFPA 70.1.2这些要求涵盖的设备采用密封式制冷剂电机压缩机和风冷或水冷式冷凝器，设计用于额定电压不超过600伏的交流电路。这些要求考虑了氧气的存在和氧气管理设备的预期用途所造成的危害，但不包括可能使用该设备的顶棚（帐篷）或氧气储存和分配系统。 1.3这些要求不包括在危险场所使用的设备，如国家电气法规，NFPA 70.1.4中所定义的易燃麻醉剂，本标准的要求不考虑有益或不完全的生理或治疗效果的完整频谱。除非定义了潜在危险条件的公认限值。需要使用超过此类可接受限制的条件进行患者治疗的设备，是由持照医生使用或在其监督下使用的。此类设备应在设备上显著显示警告。1.5如果产品的特征、特性、组件、材料或系统与标准制定时使用的功能、特性、组件、材料或系统不同，且存在火灾、触电或人身伤害风险，则应使用适当的附加组件和终端对其进行评估- 为维持本标准意图最初预期的产品用户安全水平而确定的产品要求。

Please note: All interim revisions for this edition available at time of your purchase will be included.Refrigerated Medical EquipmentUL 4161 Scope1.1 These requirements cover refrigerated medical equipment such as thermia and oxygen therapy devices for use in hospitals, nursing homes, medical care centers, medical and dental offices, and similar health care facilities in accordance with the National Electric Code, NFPA 70.1.2 Equipment covered by these requirements employ hermetic refrigerant motor-compressors and air- or water-cooled condensers, designed for use on alternating current circuits rated not more than 600 volts. These requirements take into consideration the hazards resulting from the presence of oxygen and the intended use of oxygen administering equipment but do not cover the canopy (tent), or oxygen storage and distribution systems with which the equipment may be used.1.3 These requirements do not cover equipment for use in hazardous locations, with respect to flammable anesthetics, as defined in the National Electrical Code, NFPA 70.1.4 The requirements of this Standard do not consider the complete spectrum of physiological or therapeutic effects, beneficial or otherwise, except where generally accepted limits for potentially hazardous conditions are defined. Devices which necessitate the utilization of conditions exceeding such accepted limits for patient treatment are intended for use by or under the supervision of licensed medical persons. Such equipment shall be provided with warnings prominently displayed on the device.1.5 A product that contains features, characteristics, components, materials, or systems new or different from those in use when the standard was developed, and that involves a risk of fire, electric shock, or injury to persons shall be evaluated using the appropriate additional component and end-product requirements as determined necessary to maintain the level of safety for the user of the product as originally anticipated by the intent of this standard.