悬浮床使用指导手册
悬浮床
医药气动悬浮床原理医用气动颗粒悬浮床是一种新型医用病床，应用于医疗许多领域。
它的外形象个大浴缸，缸内放的不是水，而是很细的颗粒，形成颗粒床。
当经过过滤的压缩空气向上流经细颗粒时，颗粒会象水一样流动，能够产生相当大的浮力，足以使病人漂浮在流动的颗粒之上。
由于这种床靠气动和颗粒使病人悬浮起来，所以称为气动颗粒悬浮床。
当病人漂浮在流动的颗粒上时，人体与颗粒的接触面积是相当大的，而单位接触面积上的压力却很小，这样就会增加人体皮肤受压部位的血液流量，改善皮肤表面和组织的营养，加快皮肤和组织的生长愈合。
由于颗粒流态化产生的压力低于毛细血管的闭合压，受伤的皮肤表面和组织减少了压力，就会减少病人的疼痛，使病人感觉舒适。
经过过滤后温度适宜的空气通入床体颗粒料内，使得床体内温度可调，能够改善病人的治疗和恢复环境，特别适合于烧伤病人的液体复苏，以及烧伤病人创面水分的及时散失，形成干痂，减少创面的液体渗出，同时也为创面提供了干爽的环境，抑制细菌生长，减少创面细菌的繁殖，使病人不生褥疮，而且还能治疗褥疮。
优点（1）减小皮肤表面的压强，透气性好，不生褥疮，减少病人的疼痛；（2）提高皮肤表面的温度，增加皮肤表面的血液循环，有利于伤口愈合；（3）造成一个温度可控的小气候，减少病人新陈代谢的损失，防止细菌生长；（4）限制病人分解代谢产物对伤口的感染，减少抗生素的用量。
使用悬浮床与普通床的对比(1)降低了日常治疗费用约50%；(2)缩短住院治疗时间约27%；(3)降低护理工作量约46%；(4)减少药物及换洗敷料用药约56%；(5)减轻病人心理上种种不利负担。
应用范围烧伤、重症监护、外伤、皮肤科、瘫痪、外科整形矫形、肿瘤、康复老年病学、强化治疗。
本产品在北京两家三级甲等医院长达一年时间的临床，结果如下：临床试验效果分析：1、本次临床试验试验组和对照组的入选病例无年龄及性别的统计学差异，本次试验所有病例均完成随访并纳入统计，试验组和对照组脱落率均为0%，无统计学差异；2、本次临床试验试验组和对照组的治疗有效率均为100%，两组之间无统计学差别；试验组和对照组在创面愈合时间方面无统计学差异（P=0.230>0.05)；3、试验组和对照组的不良事件发生率为0%，无统计学差别，受试产品具有和已上市产品相同的安全性；4、本次试验严格遵循试验方案，评价标准、统计方法合理，试验结果可靠，试验十分成功。
钢结构悬浮床的制作方法
钢结构悬浮床的制作方法
1、首先，购买钢结构悬浮床所需的材料，包括悬浮床的支撑架、支撑架的螺栓、支撑架的支撑棒、支撑棒的支撑架、支撑棒的支撑垫、支撑垫的螺栓、支撑垫的支撑棒、床板、床板的螺栓、床板的支撑棒等。
2、准备工具：电钻、砂纸、水平仪、钳子、扳手等。
3、准备钢结构悬浮床的支撑架，并将支撑架的支撑棒安装在支撑架上，然后将支撑棒的支撑垫安装在支撑棒上，并用螺栓固定。
4、将支撑垫的支撑棒安装在支撑垫上，并用螺栓固定，然后将床板安装在支撑棒上，并用螺栓固定。
5、最后，使用水平仪检查悬浮床的水平度，调整支撑架的高度，确保悬浮床的水平度，安装完成。
RF 浮动床控制阀安装、维护、使用手册说明书
RF20、RF50RF 双罐侧装浮床控制阀安装使用说明扫描电子版为最新RF20安装动画RF50安装动画RF 切换动画盐水流量计电动阀吸盐和补水盐水流量计电动阀维修拆卸工艺流程动画一、控制器操作使用说明（1）RF控制器工位显示说明（2）RF控制器设定界面”和“”、在时间模式“示之间进行切换。
、多路阀切换到下一工位。
、屏幕出现参数设定界面，确认和退出G、：数字加二、安装1、内部管道安装：图1：RF20控制阀设备内部管道安装图2：RF50控制阀设备内部管道安装图3：RF控制器连线图图4：RF20控制阀软水器平面布局图5：RF20控制阀进出水、排污、供电系统设置和安装图6：RF50控制阀进出水、排污、供电系统设置和安装2、设备自动启停水箱液位控制A、控制器直接输出：当收到水箱上水位闭合信号时控制器控制进水电磁阀或电动阀关闭，控制器显示“水位已满”。
此输出为+12V有源信号，不能接入高压回路图7：RF20/RF50控制器输出液位控制图8：单节点浮球开关B、单接点水位开关、给水泵的联动控制图9：RF20外接单接点液位开关、给水泵联动接线图图10：RF50（进水电动阀）内部输出单接点软化水箱液位开关、给水泵接线盒C、附加继电器实现双接点水位开关、给水泵的联动控制RF软水器的水位控制为一个12V的有源接点，需要外界一个无源接点来控制，该接点闭合时，控制器停止工作，当水位开关采用上水位（常闭NC）下水位（常开NO）位的浮球开关时，需要一个小型继电器（如正泰HH54P/220VAC）进行转换。
图11：RF20/RF50内部输出双接点水位开关、给水泵联动接线图图12：双接点浮球开关3、设备安装注意事项1、进水安装过滤器，以免杂质进入电磁阀、多路阀、布水器。
2、应保证出水压力恒定，出水管道不安装阀门，软化水箱不安装浮球阀。
3、进水压力始终不低于设备高度，设备由地面水池水泵供水，进水管道安装止回阀，防止水泵停止设备水倒流。
悬浮物测定仪安全操作及保养规程
悬浮物测定仪安全操作及保养规程为确保悬浮物测定仪的正常运行，保障操作人员的人身安全，需要严格遵守以下安全操作规程：安装1.安放地点应平整、稳固，并具有良好的通风条件。
2.需要将悬浮物测定仪安装在室内环境，避免遭受强光照射和强风吹拂。
3.悬浮物测定仪与电源应该保持适当的距离，以防止其他机械、设备或电源设备的电磁干扰。
操作1.熟练掌握悬浮物测定仪的相关使用方法，并遵循操作手册的规定进行操作。
2.严禁在悬浮物测定仪操作过程中离开操作区域，特别是禁止在操作过程中前往其他区域或离开使用区域。
3.在保证安全的前提下，必须按照规章制度要求使用标准耳塞和眼罩。
保养1.定期检查悬浮物测定仪存在的问题或损坏，并及时清理器件表面清尘，确保其处于干净整洁状态。
2.在不适用悬浮物测定仪时，应切断电源，并妥善保管其相关备件及相关零配件。
3.定期更换悬浮物测定仪的原部、耗材及消耗品，并确保所更换的零部件符合同等质量标准。
注意事项1.在悬浮物测定仪使用完毕后，应关闭电源开关，并确认仪器处于关闭状态。
2.严禁将悬浮物测定仪用于违法操作或非法用途，并责任意料。
3.使用过程中查看操作手册并按照学习规程进行使用。
总结悬浮物测定仪是一种高精度、精密的实验设备，使用过程中需要严格按照使用规程进行操作，以确保操作人员的安全和设备的运行效果。
除此之外，定期的保养和维护也是确保设备长时间、高效运行的重要保障。
为了保证仪器使用效果，我们应该长期关注生产线的相关性检测，只有这样，才能够达到我们使用仪器的预期效果。
气浮设备操作规程
气浮设备操作规程一、概述气浮设备是一种常用于水处理系统中的设备，通过利用气泡的浮力来分离悬浮物质，提高水质。
为了确保气浮设备的正常运行和安全性，制定本操作规程。
二、设备操作要求1. 操作人员应具备相关的操作技能和知识，了解气浮设备的结构和工作原理；2. 在操作前应检查设备是否正常运行，如有异常应及时报修；3. 操作人员应穿戴好个人防护装备，包括安全帽、防滑鞋、防护眼镜等；4. 操作人员应按照设备操作流程进行操作，不得随意更改设备参数；5. 在操作过程中，应注意设备周围的安全环境，确保设备周围无杂物和障碍物。
三、设备操作流程1. 开机准备a. 检查设备电源是否正常，确认电源开关处于关闭状态；b. 检查设备的水源和气源是否正常供应，如有异常应及时处理；c. 检查设备的控制面板是否正常，确认各指示灯、按钮、开关等是否正常。
2. 设备启动a. 打开设备电源开关，确认设备电源正常供应；b. 打开水源和气源开关，确保水源和气源正常供应；c. 按照操作手册调整设备参数，如气泡大小、浮力等；d. 启动设备，观察设备运行是否正常，如有异常应及时停机检修。
3. 操作过程a. 根据实际情况调整设备参数，以达到最佳处理效果；b. 定期检查设备的水质和气泡效果，如发现异常应及时调整；c. 定期清理设备内部的污泥和杂物，保持设备的清洁和畅通；d. 注意设备的运行状态，如发现异常声音、异味等应及时处理。
4. 停机操作a. 停止水源和气源供应；b. 关闭设备电源开关；c. 清理设备周围的杂物和污泥；d. 记录设备的运行情况和处理效果。
四、设备维护要求1. 定期检查设备的电气系统，确保电气设备正常运行；2. 定期检查设备的水泵、气泵等机械设备，如有异常应及时维修；3. 定期清洗设备内部的滤网、气泡发生器等部件，保持设备的正常运行；4. 定期更换设备的易损件，如密封圈、橡胶管等；5. 定期进行设备的保养和润滑，延长设备的使用寿命。
悬浮床使用指导手册
目录一.工作原理二.适应症三.禁忌症四.操作步骤五.注意事项六.终末处理一.工作原理分为沙粒悬浮床和空气搏动悬浮床.沙粒悬浮床内装入了600公斤由硅和陶瓷合成的细沙。
每粒沙直径只有50-150微米，细微得用肉眼看不见。
陶瓷粉、硅胶和碳酸钙粉等组成的特殊颗粒释放出的钠离子可使舱内的PH值维持在9-10左右，提供碱性环境，以减少细菌污染）充满流动舱，当经过过滤、加热后的压缩空气进入流动舱后，使微颗粒产生管状的自下而上的单一方向气泡流动效果，从而达到悬浮、按摩病人的作用，并吸附病人的渗出液。
吸附后的微颗粒，由于重力的原因而沉降到舱底。
如此循环反复，不但保证了特殊颗粒的流动，而且从根本上阻止了细菌的繁殖和交叉感染，从而有效地保证在工作状态下，局部的消毒环境。
该床还分别带有干燥功能，可以及时烘干伤员伤口的渗出液，避免感染和长褥疮。
悬浮床的应用大大缓解了烧伤病人的痛苦，也使创面愈合时间大大缩短。
二.适应症1.大面积烧伤2.躯干后侧或臀部烧伤3.背/腰/臀慢性溃疡或压疮4.手术后不宜搬动的病人5.危重或者瘫痪患者6.创伤后拌有骨折或脱位三.禁忌症1.体重超过150公斤2.伴脊柱瘫痪的患者四.操作步骤1.启动悬浮床预热,至设定的温度(一般为30～36℃之间)2.床体上铺设床单及烫单,以免渗液渗透3.患者仰卧于悬浮床上,如有会阴部或者双上下肢烫者,应伸展四肢,呈”大”字型.4.头面部肿胀者调节靠背垫,视情况调节高度五.注意事项1.由于悬浮床的构造特别，浮动的床面使患者本已存在的恐惧和疑虑心理加剧，使患者的心理更加脆弱，此时作为医务人员要理解病人的痛苦，要有高度的责任心和耐心向患者介绍该床的构造和治疗作用，并讲明此床本身是具有保暖作用的。
2. 床温的监测密切观察操作屏上的温度，如床温高于所设定的温度，需检查制冷系统运行是否正常及排水管道有无排水散热的现象;如床温低于设定的温度，需观察产热系统是否运行正常，排水是否停止。
磨浮设备安全操作规程
磨浮设备安全操作规程一、前言磨浮设备是一种用于浮选工序的设备，广泛应用于矿山、冶金、化工等行业。
为了保障生产过程的安全性和人员的身体健康，制定了以下磨浮设备安全操作规程。
二、设备操作前的准备工作1. 设备检查：操作人员在每次使用设备前，应对设备进行全面检查，主要检查设备的电气设施是否完好稳定，机械部件是否正常运转，密封装置是否严密等。
2. 设备放置：操作人员在选择设备摆放位置时，应确保设备周围无阻碍物，便于操作和维修。
3. 仪表检查：操作人员应对设备的仪表进行检查，确保其正常工作。
三、设备的安全操作1. 操作顺序：在操作设备之前，需要按照确定的操作顺序，确保每个步骤的顺利进行。
2. 人员佩戴：操作人员在操作设备时，必须佩戴符合安全规定的个人防护装备，包括安全帽、防护眼镜、防护服等。
3. 设备开启：在操作设备之前，应按照操作规程将设备开启。
4. 操作注意事项：(1) 严禁将人体部位伸入设备内部或机械运转部位，在设备运转过程中要保持一定距离。
(2) 禁止将易燃易爆物品靠近设备及其电气线路，以免引发火灾事故。
(3) 禁止在设备运转过程中操作中断器、开关等电气设备。
(4) 禁止擅自调整设备的参数，如需调整，须得到相关人员的指导和同意。
5. 设备关闭：操作人员在操作完毕后，应按照操作规程将设备关闭。
6. 设备保养：定期对设备进行保养和维修，确保设备的正常运行和安全性。
四、应急措施1. 火灾事故：如发生火灾事故，应立即按规定方式通知消防部门，并按照应急预案进行安全疏散。
2. 气体泄漏事故：如发生气体泄漏事故，应立即通知相关部门，迅速疏散人员，并戴上呼吸器进行自救。
3. 电气事故：如发生电气事故，应立即切断电源，并通知维修人员进行处理。
4. 人员伤害事故：如发生人员伤害事故，应立即进行急救，并通知相关部门进行处理。
五、操作人员的安全常识1. 操作人员应严格按照操作规程进行操作。
2. 操作人员应定期参加相关的安全培训，提高安全意识和技能。
悬浮床支持椅说明书
TABLE OF CONTENTSSymbol Reference ..........................................................2Intended Use and Precautions ........................................3Part Identification – Evacuation HoverJack® ....................4Instructions for Use ........................................................5Product Specifications/Required Accessories ..................6Part Identification – HT-Air® Air Supply ...........................7HT-Air® Keypad Functions ..............................................7Air200G/Air400G Air Supplies ........................................7Cleaning & Preventive Maintenance ..............................8User ManualSymbol ReferenceCE MARKING OF CONFORMITYUK MARKING OF CONFORMITYAUTHORIZED REPRESENTATIVEUK RESPONSIBLE PERSON SWITZERLAND AUTHORIZEDREPRESENTATIVECAUTION / WARNINGMANUAL CLEANINGIMPORTERDISPOSAL FASTEN PATIENT SAFETY STRAPFOOT ENDKEEP DRYLATEX FREEMANUFACTURERDATE OF MANUFACTUREMEDICAL DEVICEMODEL NUMBERSERIAL NUMBERDO NOT LAUNDERUNIQUE DEVICE IDENTIFIERPATIENT WEIGHT LIMITIntended Use and PrecautionsINTENDED USEThe Evacuation HoverJack® Device is used to transport patients up or down stairs in the event of an emergency. The Evacuation HoverJack can also be used to lift a patient in supine position from the floor to bed or stretcher height, utilizing the HoverTech Air Supply to inflate each of the four chambers.INDICATIONS• Patients unable to assist in their own vertical lift or evacuation, such as after a fall or in an emergency situation.• Patients whose weight or girth poses a potential health risk for the caregivers responsible for lifting or moving said patients.• CPR compatible when fully inflated.CONTRAINDICATIONS• Patients who are experiencing thoracic, cervical or lumbar fractures that are deemed unstable should not use the Evacuation HoverJack unless a clinical decision has been made by your facility.INTENDED CARE SETTINGS• Hospitals, long term or extended care facilities.PRECAUTIONS• Make sure patient safety straps are secured before moving. Do not secure before inflation.• Move the Evacuation HoverJack using the transport straps and/or the transport handles located along the top perimeter.• Never use patient safety straps to pull the Evacuation HoverJack, as they may tear.• When moving a patient on the inflated Evacuation HoverJack, use caution and move slowly.• Additional caregivers are recommended when moving or evacuating a patient over 350 lbs./159 kg. • Never attempt to move a patient on an uninflated Evacuation HoverJack.• Never leave a patient unattended on an inflated device.• Use this product only for its intended purpose as described in this manual.• Only use attachments and/or accessories that are authorized by HoverTech International.WARNING/CAUTION• Always use a minimum of two caregivers while inflating/transporting the Evacuation HoverJack.• A minimum of three caregivers is required for stairwell evacuation.• One caregiver should remain on the side of the patient duringinflation with the second caregiver managing inflation. If available, a third caregiver should attend to the other side of the patient.• Reference product-specific user manuals for additional operating instructions.PRECAUTIONS– HOVERTECH INTERNATIONAL AIR SUPPLY• Not for use in the presence of flammable anesthetics or in a hyperbaric chamber or oxygen tent.• Route the power cord in a manner to ensure freedom from hazard. • Avoid blocking the air intakes of the HoverTech International Air Supply.Avoid electric shock. Do not open HoverTech International Air Supply.DECLARATION OF CONFORMITYThis product conforms to the requirements of Medical Devices Regulation (2017/745).SEPARATE INFLATE/DEFLATE VALVES.[Mfg before 6/2023]Note: Two versions of Evacuation HoverJack® Air Patient LiftUNIVERSAL VALVES.[Mfg after 6/2023]Part Identification - Evacuation HoverJack® [Manufactured before 6/2023]Evacuation HoverJack® Instructions for Use as an Air Patient Lift1. Place Evacuation HoverJack® on the floor next to the patient, makingsure the chamber with Valve #4 is on the top and the chamber with Valve #1 is against the floor.2. Make certain that all four red-capped deflation valves are cappedtightly or Universal Valves are closed BEFORE INFLATING.3. Log roll patient onto the deflated Evacuation HoverJack, and positionpatient with feet at the valve end where indicated. Alternatively, the patient can be placed on top of the Evacuation HoverJack using theHoverMatt® Air Transfer System (see HoverMatt manual for instructions).If the HoverMatt is used, make certain that the HoverMatt and patient are properly centered on the Evacuation HoverJack. Always deflate the HoverMatt prior to inflating the Evacuation HoverJack.4. Always use a minimum of two caregivers while using the EvacuationHoverJack during inflation/transport.5. One caregiver should remain on the side of the patient duringinflation with the second caregiver managing inflation. If available, a third caregiver should attend to the other side of the patient.6. Plug the HoverTech International Air Supply power cord into anelectrical outlet.7. Caregiver at foot end turns on HoverTech International Air Supply toinitiate air flow.8. To begin inflation hold hose against valve #1 of Evacuation HoverJack(valve closest to the floor).9. When fully inflated, remove hose. Chamber remains inflated.10. Secure patient safety straps.11. Using the same process: move to valve #2, valve #3 and valve #4in exact succession, or until Evacuation HoverJack reaches desiredheight.12. Turn off HoverTech International Air Supply, and attach valve caps, ifdesired and applicable.13. Move Evacuation HoverJack to desired location.14. If transferring from the Evacuation HoverJack onto an adjacent surface,unbuckle patient safety straps.15. If it is necessary to lower patient, slowly open the uppermost valve.When chamber is fully deflated, move in succession downwards to fully deflate. Depress center button for slower deflation.CHAMBERS MUST BE FULLY INFLATED TO ENSURE STABILITY.DO NOT RELEASE MULTIPLE CHAMBERS AT ONCE WHENLOWERING A PATIENT.Evacuation HoverJack® Instructions for Use as an Evacuation Device1. To inflate, follow steps 1-11 of instructions for use as an air patient lift.2. Unzip foot pouch and position Evacuation HoverJack as close aspossible to adjacent surface.3. Transfer patient from bed or stretcher onto Evacuation HoverJack.4. Ensure that the patient’s body is centered, and zip foot pouch.5. If necessary, inflate the head-end wedge.6. Using the buckles, secure safety straps over the patient and adjustuntil taut.7. Using foot end transport straps and handles located around theperimeter of the Evacuation HoverJack, pull patient to the neareststairwell, and position the Evacuation HoverJack so the patient can be taken down the stairs feet first.8. Before descending the stairs, chambers 3 and 4 must be fullydeflated. To release air, slowly open valve #4. When chamber #4 is fully deflated, repeat the process for chamber #3. DO NOT RELEASE MULTIPLE CHAMBERS AT ONCE. 9. Retighten patient safety straps after deflating chamber #3 and #4 toensure patient is secure.10. Caregiver at head end will control evacuation using head endtransport straps. Caregiver at head end should be physically stronger.11. While 2 caregivers hold the head end transport straps and handles,the footend caregiver will begin to pull the patient down the stairs with the foot end transport strap. The Teflon-infused bottom material will allow the Evacuation HoverJack to slide down each flight. Ifnecessary, the footend caregiver can use their thigh to brace theEvacuation HoverJack and slow the descent. Once at ground level, move the patient to safety.ENSURE THAT PATIENT REMAINS CENTERED ON THEEVACUATION HOVERJACK, AND THAT THEIR HEAD DOESNOT SLUMP FORWARD AND RESTRICT BREATHING DURINGEVACUATION.A MINIMUM OF THREE CAREGIVERS (TWO AT HEADEND ANDONE AT FOOTEND) SHOULD BE USED TO EVACUATE PATIENTDOWN STAIRS).Product Specifications/Required AccessoriesMaterial:Topside Material: Nylon oxford Underside Material: Teflon®Construction:RF-WeldedWidth:32” (81cm)Length:72” (183 cm)Height:30” (76 cm) Inflated [each chamber 7 1/2” (19 cm)] Model #: HJ32EVWeight limit: 1200 lbs (544 kg) for vertical lift.Weight limit: 700 lbs (318 kg) for stairwell evacuation. REQUIRED ACCESSORY:Model #: HTAIR1200 (North American Version) – 120V~, 60 Hz, 10A Model #: HTAIR2300 (European Version) – 230V~, 50 Hz, 6AModel #: HTAIR1000 (Japanese Version) – 100V~, 50/60 Hz, 12.5A Model #: HTAIR2356 (Korean Version) – 230V~, 50/60 Hz, 6AModel #: Air200G (800 W) (North American Version) – 120V~, 60 Hz, 10A Model #: Air400G (1100 W) (North American Version) – 120V~, 60 Hz, 10APart Identification – HT-Air® Air SupplyAir Filter CoverHose NozzleHoseHose Release ButtonControl Panel LabelCarrying Handle/Attachment HookPower Cord StrapPower Cord (US/UK/Euro)WARNING: T he HT-Air is not compatible with DC power supplies.The HT-Air is not for use with the HoverJack Battery Cart.HT-Air® Keypad FunctionsTransfer Speed HighAdjustable/ Pressure SettingTransfer Speed LowStandby (Amber LED)Power IndicationAdjustable SpeedIndication(Green Flashing LED)Green LEDsADJUSTABLE: For use with HoverTech air-assisted positioning devices. There are four different settings. Each press of thebutton increases the air pressure and rate of inflation. The Green Flashing LED will indicate the inflation speed by the number of flashes (i.e. two flashes equals the second inflation speed). All of the settings in the ADJUSTABLE range are substantially lower than the HoverMatt and HoverJack settings. The ADJUSTABLE function is not to be used for transferring.The ADJUSTABLE setting is a safety feature that can be used to ensure the patient is centered on HoverTech air-assisted devices and to gradually accustom a patient who is timid or in pain to both the sound and functionality of the inflated devices. STANDBY: Used to stop inflation/air flow (Amber LED indicates STANDBY mode).HOVERMATT 28/34: For use with 28" & 34" HoverMatts and HoverSlings.HOVERMATT 39/50 & HOVERJACK: For use with 39" & 50" HoverMatts and HoverSlings and 32" & 39" HoverJacks.Air200G/Air400G Air SuppliesIf using HoverTech’s Air200G or Air400G Air Supplies, press the grey button on the top of the canister to initiate air flow. Press the button again to stop air flow.Cleaning & MaintenanceEVACUATION HOVERJACK CLEANING INSTRUCTIONSIn between patient use, the Evacuation HoverJack should be wiped down with a cleaning solution used by your hospital for medical equipment disinfection. A 10:1 bleach solution (10 parts water: one part bleach) or disinfectant wipes can also be used. NOTE: Cleaning with bleach solution may discolor fabric.First remove any visible soil, then clean the area according to the cleaning product manufacturer’s recommended dwell time and level of saturation. A gentle scrub brush can also be used on the affected area, if necessary, to help penetrate the Evacuation HoverJack material.Do not launder the Evacuation HoverJack.PREVENTIVE MAINTENANCE INSTRUCTIONSThe Evacuation HoverJack should be periodically inspected to ensure the following:• All patient safety straps are attached.• Transfer handles are all attached.• All buckles and zippers are intact and operational.• There are no punctures or tears.Evacuation HoverJack with separate inflate/deflate valves:• Inflate valves are all self-sealing with no evident leakage. • All deflate valves are equipped with a red cap.• The red caps are intact.Evacuation HoverJack with Universal Valves:Universal valves open fully and close tightly.AIR SUPPLY CLEANING AND MAINTENANCESee air supply manual for reference.NOTE: CHECK YOUR LOCAL/STATE/FEDERAL/INTERNATIONAL GUIDELINES BEFORE DISPOSAL.Transportation and StorageThis product does not require any special storage conditionsReturns and RepairsAll products being returned to HoverTech International (HTI) must have a Returned Goods Authorization (RGA) number issued by the company. Please call (800) 471-2776 and ask for a member of the RGA Team who will issue you an RGA number. Any product returned without an RGA number will cause a delay in the repair time.Returned products should be sent to:HoverTech International Attn: RGA # ___________ 4482 Innovation Way Allentown, PA 18109For European companies, send returned products to:Attn: RGA #____________ Kista Science TowerSE-164 51 Kista, SwedenEtac Ltd.Unit 60, Hartlebury Trading Estate, Hartlebury, Kidderminster, Worcestershire, DY10 4JB +44 121 561 2222Promefa AGKasernenstrasse 3AHartlebury, Kidderminster, 8184 Bachenbülach, CH +41 44 872 97 79CEpartner4U, ESDOORNLAAN 13, 3951DB MAARN, THE In case an adverse event in relation to the device, incidents should be reported to our authorized representative. Our authorized representative willforward information to the manufacturer.HoverTech International 4482 Innovation Way Allentown, PA 18109 ******************These products comply with the standards applicable for Class 1 products in the Medical Device Regulation(EU) 2017/745 on medical devices.For product warranties, visit our website: https:///standard-product-warranty/4482 Innovation Way Allentown, PA 18109 800.471.2776Fax 610.694.9601 ******************。
潮流北美漂浮池水泵系统操作说明及零件手册说明书
DescriptionThis pump system is designed for decorative use and canimprove water aeration. It produces water fountains up to 15’ in height, and up to 4,900 gallons of water per hour. Make your floating fountain system even more dramatic at night by adding the NightBright lighting system 023069.Operates in 5 feet of water or deeper.UnpackingWhen unpacking the unit, inspect carefully for any damage that may have occurred during transit.Floating Pond Pump SystemModels FPS0501 and SPS0501Operating Instructions & Parts ManualPlease read and save these instructions. Read carefully before attempting to assemble, install, operate or maintain the product described. Protect yourself and others by observing all safety information. Failure to comply with instructions could result in per-sonal injury and/or property damage! Retain instructions for future reference.FW07790909 Supersedes0408General Safety InformationCarefully read and follow all safety instructions in this manual and on pump. Keep safety labels in good condi-tion. Replace missing or damaged safety labels.This is a SAFETY ALERT SYMBOL. When you seethis symbol on the pump or in the manual, look for one of the following signal words and be alert to the potential for personal injury or property damage.Warns of hazards that WILL cause seriouspersonal injury or death, if ignored.Warns of hazards that MAY cause minorpersonal injury, product or property damage if ignored.IMPORTANT: Indicates factors concerned with operation, installation, assembly or maintenance which could result in damage to the machine or equipment if ignored.NOTE: Indicates special instructions which are important but are not related to hazards.Never enter the watereither wading, swimming or in a boat with thepump power on, as this may result in severecarefully. Failure to follow could result in serious bodilyinjury and/or property damage.shall be in accordance with National ElectricCode (NEC) and all applicable local codesand ordinances. A licensed electrician shouldperform installation.“NO SWIMMING” ANDOR WARNING SIGNS SHOULD BE POSTED PERSTATE AND LOCAL CODES.Please affix included warning label to powerreceptacle or junction box.100ft power cord with three prong GFI plug. –Must connect to properly grounded receptacleof grounding type. Do not remove groundpin on plug. Do not extend the cord length by splicing orTHIS UNIT, WITH THE GFI, TO A PROPERLYGROUNDED RECEPTACLE MAY RESULT INto a circuit equipped with a fuse or circuitbreaker of ample capacity.Always disconnect powersource before performing any work on ornear the motor or its connected load. If thepower disconnect point is out-of-sight, lock itin the open position and/or tag it to prevent unexpectedapplication of power. Failure to do so could result in fatalelectrical shock or bodily injury.DO NOT handle pump withwet hands or when standing in water asfatal electrical shock could occur. Disconnectmain power supply before handling systemfor any reason.from coming in contact with sharp objects,oil, grease, hot surfaces or chemicals. DONOT kink the power cable. If damagedbox, fused disconnect switch, or covers open(either partially or completely) when notbeing worked on by a competent electricianor repairman.Always use caution whenoperating electrical controls in damp areas.If possible, avoid all contact with electricalequipment during thunderstorms or extremedamp conditions.equipment in protected area to preventmechanical damage which could produce seriouselectrical shock and/or equipment failure.DO NOT use this system topump flammable liquids such as gasoline, fueloil, kerosene, etc. Failure to follow the abovewarning could result in property damage and/or personal injury.Do not pump water above 120 degreesFahrenheit.Water leaving nozzle is at high velocityand can cause bodily injury if contact is made.in swimming pool areas.!to the State of California to cause cancer and birth defects orother reproductive harm.!coming out the bottom and protected from direct rainfall.INSTALLATION INSTRUCTIONS1. Only install this system in ponds where no swimming,wading, boating or fishing is allowed while fountain isoperating. Disconnect power to pump before fishing orentering the water.2. Post appropriate warning signs per local and state codes.3. Inspect pump system for damage before installing inpond. Check that all bolts and screws are tight. Check forany bent prongs or a cracked case on the GFI.4. The unit ships with one spray nozzle attached. To changeto one of the other 2 nozzles, remove the 4 screws fromthe nozzle then replace with desired nozzle. Refer toFigures 1, 2 & 3 for spray pattern appearance. Nozzlesare marked “This side up.” Make sure the o-ring isseated in groove before installing nozzle. Tighten screwsuntil seated, approximately 10 to 12 in-lbs.5. Attach nylon anchor ropes to 3 eyebolts located at topof screen. Secure (make sure rope is tight) to weightsplaced on pond floor or stakes on pond shore. Whenusing weights to anchor the pump, place weightsapproximately 10 feet from unit. Alternately, two anchorropes placed 180 degrees apart can be used, but 3 ropeswill provide the best stability.6. Before connecting the unit to the power receptacle,check to insure there is no leakage to ground. This canbe done by using an ohm meter and setting the scale toits highest setting (i.e. Rx100K). Connect one ohmmeter lead to the unit power cord ground (round prong) and to one of the flat prongs. It should read infinite or at least 2 mega ohms. Repeat with the other prong. If reading is below 2 mega ohms on either prong contact Customer Service Help Line listed at bottom of page.7. Do Not Operate System on an Extension Cord. If no power is accessible at the pond, contract a licensed electrician to install the proper power supply in accordance with National Electric Code and all applicable local codes and ordinances.8. After installing the unit, checking ground andconnecting power to the unit, the unit can be powered up. Check operation of the GFI by pushing the “Test” button, the unit should stop. Pushing the “Reset” button should restart the unit. If pressing the “test” button does not stop the unit, immediately shut off power to unit and contact Customer Service Help Line listed at bottom of page.NOZZLE PATTERNST h is s id eu p Figure 1: Water Lily - An eye-catching combination spray. Item #2AT h i s s id eu pFigure 2: Sky Cannon - A dramatic single plume of water. Item #2BT h i s s id eu pFigure 3: Water Trumpet - A symmetrical inverted bell shape.Item #2CFigure 4: Typical InstallationINSTALLATION CHECK LIST☐ Read installation instructions and warnings ☐ Post appropriate warning signs ☐ Install desired spray nozzle ☐ Install and anchor unit in pond☐ Check insulation resistance to ground ☐ Power up unit☐ Test operation of GFI by pressing the “Test” Button.☐ File instructions for future reference REQUIRED TOOLS & SUPPLIES• #2 Phillips screwdriver • Nylon rope to anchor unit• Stakes or weights for anchoring unit• Ohm meter to check insulation resistance to groundWINTER STORAGE• Rinse unit with clean water to remove any build-up on unit.• Check unit for any damage.• Store unit in heated space in freezing climates.The pump motor is water lubricated and is factory filledwith an antifreeze solution. During operation the antifreeze may exchange, thru the filtered check valve, with the pond water. In climates where freezing may occur, the unit must be stored in a heated storage space to prevent damage to the motor.TROUBLESHOOTING GUIDE PROBLEM POSSIBLECAUSESCORRECTIVE ACTIONUnit won’t run Circuit break-er trippedReset circuit breaker GFI Tripped Reset GFINo or low spray Blockedscreen ornozzle, miss-ing or dam-aged o-ring,or incorrectlyinstallednozzleDisconnect power. Clean screenand/or nozzle. Check that o-ring isundamaged and seated in groove.Check that nozzle is installed prop-erly (nozzles are marked “This sideup”). Check depth of pond. If lessthan 5 feet deep, move to deepersection. Restart unit.GFI Trips Electricalstorm can tripGFIReset GFIShort in sys-tem Disconnect power and check cord for damage. If cord is damaged contact Customer Service Help Line listed at bottom of page for replacement.Unit spins Anchor ropeloose Check anchor rope and re-attach if necessaryItem #Qty Part No.Description16021624Screw - #10 x 3/4 Pan Head High-Low 2A1021617Nozzle - Water Lily2B1021618Nozzle - Sky Cannon2C1021619Nozzle - Water Trumpet31021622O-Ring - AS568A - 041 (3” ID x 3/18” OD) 44021628Bolt - SS 1/4-20 x 3/454021629Lockwasher - 1/4”61021707Mounting Flange71021534Float81021713Pump End91021740Motor 1/2 HP 115V104127021Locknut - SS 5/16-24111021715100 ft. power cord with GFI11A1021614GFI123021609Eye Bolt - SS 1/4-20 x 2-1/2133021623Locknut - SS 1/4--20141021608Screen151021611Screen Cap161021613Strain Relief172021625Warning DecalFlow (GPH)Spray Height(Ft.)PatternImagePatternName 490015Thissi de upIL053Thissi de upThissi de upWater Lily- 2A 330015Sky Cannon- 2B 270013WaterTrumpet - 2C15161112(A/B/C)345671710911131214811A。
悬挂式患者床垫操作手册说明书
E m e r g e n c y R e l i e f B e d ™OperationsManual3019S y m b o l sS u m m a r y o f s a f e t y p r e c a u t i o n sW A R N I N GThe personal safety of the patient or user may be involved.Disregarding this information could result in injury to the patient or user.C A U T I O NThese instructions point out special procedures orprecautions that must be followed to avoid damaging the equipment.W A R N I N G•Do not sit directly on the ends of the bed.Excessiveweight will cause the litter surface to tip up,possibly causing patient injury.•Always apply the caster brakes when a patient isgetting on or off the bed.Push on the bed to ensure the brakes are securely locked.Always engage the brakes unless the bed is being moved.Injury could result if the bed moves while a patient is getting on or off the bed.•The maximum weight limit of the device is 350lb.Aweight beyond this limit could cause the device to break or collapse resulting in patient injury.•Push the bed with the foot bar handle when the patientis prone to avoid injury to the end user.You can also push the bed from the head end when the Fowler (head end of patient support surface)is raised.•Use caution when moving the bed when occupiedbecause there are no restraints or siderails.•Do not use the IV pole as a push/pull device.Productdamage may occur.P r o d u c t d e s c r i p t i o nThe E m e r g e n c y R e l i e f B e d is a non-powered,manual adjustable hospital bed that is used in combination with a patient support surface and includes an IV pole.The non-powered patient support surface fits the dimensions of the frame.This basic bed and surface were developed in response to the shortage of hospital beds during the COVID-19pandemic.I n d i c a t i o n s f o r u s eThe E m e r g e n c y R e l i e f B e d is intended to assist with positioning,therapy,recovery,support,and transport of patients within a general hospital or in a temporaryemergency environment during a local,state,or federal-declared situation.The product is intended to be used only for the duration of the COVID-19pandemic.The non-powered support surface is intended to provide a support surface for treatment and examination of a patient.P r o d u c t i l l u s t r a t i o nE BACEDF GGA Foot bar handleB FowlerC IV poleD IV pole socketE Brake casterF Gusset plateG Retainer plateI n s e r t i n g t h e I V p o l e1.Remove the rue ring cotter and clevis pin from the IVpole socket(D).2.Insert the IV pole(C)into the IV pole socket.3.Reinstall the rue ring cotter and clevis pin to securethe IV pole in the IV pole socket.C l e a n i n gRecommended cleaning method:1.Hand wash all exposed surfaces of the product with amild detergent by spray or pre-soaked wipes.2.Follow the cleaning solution manufacturer’sinstructions for appropriate contact time and rinserequirements.3.Dry the product before you return it to service.N o t e-Avoid oversaturation.Do not allow the product to remain wet.D i s i n f e c t i n gRecommended disinfectants for this product’s surfaces include the following:•Quaternary(active ingredient-ammonium chloride) that contain less than3%glycol ether•Phenolic(active ingredient-o-phenylphenol)•Chlorinated bleach solution(5.25%-less than1part bleach to100parts water)•Alcohol(active ingredient-70%isopropyl alcohol) Recommended disinfection method:1.Follow the disinfectant solution manufacturer’sdilution recommendations.2.Apply the recommended disinfectant solution by sprayor pre-soaked wipes.3.Hand wash all exposed surfaces of the product withthe recommended disinfectant.4.Dry the product before you return it to service.N o t e•Avoid oversaturation.Do not allow the product to remain wet.•Follow the manufacturer’s dilution recommendations for appropriate contact time and rinsing requirements.Follow the chemical manufacturer’s guidelines forproper disinfecting.B e d f r a m e a s s e m b l yT o o l s r e q u i r e d:•Rubber mallet(optional)to install bolts,if needed •Scissors,knife,or wire snips to cut zip ties•Table surface–15cm x75cm recommended(130kg weight capacity to support70kg bed)T o o l s f o r l o w v o l u m e a s s e m b l y:•M8ratchet wrenchT o o l s f o r h i g h v o l u m e a s s e m b l y:•Drill driver•Drill driver setting14-17•M8deep socket•150mm long hex power drive extension with3/8”male squareN o t e-Do not use a shorter extension to avoidinterference between the tool and the bed frame.I m p o r t a n t:Two people are needed to lift,move,and flip the beds during assembly.N o t e-The bed frames are stacked upside down on the pallets at delivery.1.With two people,rest the bed frame upside down on atable surface.2.Install the bolts onto the bottom of the bed.N o t e•The bed frame is longer and wider than this table size to allow for overhang of the installed parts.•Rest the bed on a high surface to keep these parts from touching the floor:#8caster tubes,#7castertubes,and mattress retainer plates.These partsextend above the top of the litter skin.Install these items with the bed frame upside down on the table:•Two foot end caster assemblies•Two head end caster assemblies•Three mattress retainer platesF o o t e n d c a s t e r a s s e m b l y1.Hand tighten four short bolts and four nuts(two perside)to install two gusset plates(one per side).2.Check that all casters are the same model type.3.Note the location of the no brake(A)and brake(B)type.Assemble the no brake(A)casters diagonally to each other.Assemble the brake(B)castersdiagonally to each other.4.Install two tube#8caster assemblies(one per side).Face the engraved#8on the tubes toward the litterskin.5.Hand tighten four short bolts and four nuts first(twoper side).6.Fully tighten all eight nuts.ABH e a d e n d c a s t e r a s s e m b l y1.Note the location of the no brake(A)and brake(B)type.Assemble the no brake(A)casters diagonally toeach other.Assemble the brake(B)castersdiagonally to each other.2.Install two head plates and two tube#7casterassemblies(one per side).Face the engraved#7on the tubes toward the litter skin.3.Hand tighten six medium bolts and six nuts(three perside).4.Fully tighten all six nuts.ABM a t t r e s s r e t a i n e r p l a t e a s s e m b l y1.Position the mattress retainer plates to extend towardthe patient side of the bed.2.Install two mattress retainer plates(no Stryker label)on the#16side tubes(one per side).3.Hand tighten four medium bolts and four nuts(two perside).4.Position the mattress retainer plate to extend towardthe patient side of the bed.5.Install one mattress retainer plate(with Stryker label)on the#10foot end tube.The Stryker label facestoward the outside of the bed at the foot end.6.Hand tighten two medium bolts and two nuts.7.Fully tighten all six nuts.I m p o r t a n t:Two people are needed to lift,move,and flip the beds during assembly.With two people:1.Flip the bed over on and rest the bed on the table withthe patient side up.2.Lift the bed off the table and set the bed on the floor. Install these items with the bed upright on the floor.•Footboard tube assembly•Headboard tube assembly•IV pole(see page2)F o o t b o a r d t u b e a s s e m b l y1.Install the footboard tube#14to the litter skin side oftube#8.Face the engraved#14toward the floor.2.Hand tighten two medium bolts and two nuts.3.Fully tighten bothnuts.H e a d b o a r d t u b e a s s e m b l y1.Install the headboard tube#13to the litter skin side oftube#7.Face the engraved#13toward the floor.2.Hand tighten two medium bolts and two nuts.3.Fully tighten bothnuts.Stryker Medical3800E.Centre Avenue Portage,MI49002 USA。
自制悬浮床教学设计方案
一、教学目标1. 知识目标：了解悬浮床的原理和构造，掌握悬浮床的制作方法。
2. 技能目标：培养学生动手实践能力，提高学生的创新意识和团队合作精神。
3. 情感目标：激发学生对科学探究的兴趣，培养学生热爱科学、勇于探索的精神。
二、教学对象本课程适用于初中、高中及职业技术学校的学生。
三、教学时间2课时四、教学地点学校实验室或教室五、教学材料1. 原材料：泡沫塑料板、木条、细绳、胶带、剪刀、电钻、螺丝等。
2. 工具：尺子、铅笔、电钻、螺丝刀等。
六、教学过程1. 导入新课（1）教师简要介绍悬浮床的原理和构造，激发学生的兴趣。
（2）提出问题：如何制作一个简单的悬浮床？2. 知识讲解（1）讲解悬浮床的基本原理：利用泡沫塑料板和木条等材料，通过合理的结构设计，使床面悬浮在空中，减轻人体对床面的压力。
（2）讲解悬浮床的构造：主要包括床面、支撑架、悬挂装置等。
3. 实践操作（1）学生分组，每组选用一套材料，开始制作悬浮床。
（2）教师巡回指导，解答学生在制作过程中遇到的问题。
（3）学生根据教师讲解的原理和构造，自行设计悬浮床的结构，并尝试改进。
4. 交流展示（1）各小组展示自己的悬浮床，介绍制作过程和心得体会。
（2）教师点评各小组的作品，总结制作过程中的优点和不足。
5. 总结与反思（1）教师引导学生总结悬浮床的制作方法，强调动手实践和团队合作的重要性。
（2）学生反思自己在制作过程中的收获和不足，提出改进措施。
七、教学评价1. 评价方式：观察学生参与度、动手实践能力、创新意识、团队合作精神等方面。
2. 评价标准：根据学生的制作成果、交流展示、反思总结等方面进行综合评价。
八、教学延伸1. 引导学生思考：如何提高悬浮床的舒适度？2. 组织学生参观相关企业，了解悬浮床的制造工艺和应用领域。
3. 鼓励学生参加科技创新比赛，将悬浮床制作成果转化为实际应用。
通过本课程的学习，学生不仅能够掌握悬浮床的制作方法，还能培养动手实践能力、创新意识和团队合作精神，为今后的学习和生活奠定基础。
悬浮床故障应急预案
一、编制目的为保障悬浮床正常运行，确保生产进度不受影响，最大限度地减少设备故障带来的损失，特制定本悬浮床故障应急预案。
本预案旨在明确悬浮床故障应急响应流程、组织架构、职责分工及应急处置措施，提高悬浮床故障处理效率。
二、适用范围本预案适用于悬浮床设备在运行过程中出现的各种故障，包括但不限于电气故障、机械故障、控制系统故障等。
三、组织架构1. 成立悬浮床故障应急指挥部（1）指挥长：由生产部经理担任，负责全面协调、指挥悬浮床故障应急工作。
（2）副指挥长：由设备部经理、安全部经理担任，协助指挥长开展工作。
（3）成员：各部门负责人、悬浮床操作人员、维修人员等。
2. 成立悬浮床故障应急小组（1）组长：由设备部经理担任，负责悬浮床故障应急工作的具体实施。
（2）副组长：由生产部经理、安全部经理担任，协助组长开展工作。
（3）成员：悬浮床操作人员、维修人员、安全员等。
四、职责分工1. 指挥部职责（1）负责悬浮床故障应急工作的全面协调、指挥。
（2）组织应急小组开展故障排查、抢修工作。
（3）协调各部门资源，确保故障得到及时处理。
2. 应急小组职责（1）负责悬浮床故障的初步判断、故障原因分析。
（2）制定故障处理方案，并组织实施。
（3）对故障处理过程进行监督，确保故障得到彻底解决。
3. 操作人员职责（1）发现悬浮床故障时，立即报告应急小组。
（2）协助应急小组进行故障排查。
（3）在故障处理过程中，严格遵守操作规程，确保自身安全。
4. 维修人员职责（1）根据故障原因，进行故障排除。
（2）对故障处理过程进行记录，总结经验教训。
（3）对设备进行维护保养，预防故障发生。
五、应急处置措施1. 初步判断（1）操作人员发现悬浮床故障后，立即向应急小组报告。
（2）应急小组接到报告后，立即进行初步判断，确定故障类型。
2. 故障处理（1）根据故障类型，制定故障处理方案。
（2）组织维修人员进行故障排除。
（3）对故障处理过程进行监督，确保故障得到彻底解决。
高温高压声悬浮系统安全操作及保养规程
高温高压声悬浮系统安全操作及保养规程高温高压声悬浮系统是一种高科技的工业设备，能够在恶劣环境下进行高精度加工和检测。
然而，在操作和保养时，需要非常谨慎，以防止意外发生。
本文将介绍高温高压声悬浮系统的安全操作和保养规程，帮助您正确、安全地使用和维护这种设备。
安全操作规程1. 熟悉操作手册在使用高温高压声悬浮系统之前，必须先熟悉操作手册。
操作手册将告诉您如何正确地启动设备、进行调试、执行加工任务、关闭设备等，以及在设备出现故障时应该采取的措施和怎样进行维修。
2. 佩戴防护装备在操作高温高压声悬浮系统时，必须佩戴适当的防护装备，包括安全眼镜、安全鞋、手套等。
必须避免穿着宽松的衣物和珠宝，以及使用吸烟、喝酒等影响身体健康和工作安全的行为。
3. 进行排气准备在使用高温高压声悬浮系统之前，必须进行排气准备。
排气准备的目的是将系统中的空气排出，以便防止操作过程中的爆炸和其他意外事故。
排气前必须检查系统中是否有泄漏点，并确保安全阀是否正常工作。
4. 调整温度和压力在进行加工任务之前，必须将温度和压力调整到适当的范围内。
对于各种材料和加工过程，有不同的温度和压力要求，必须仔细按照操作手册的要求进行调整。
此外，在操作过程中还要不断监控温度和压力，确保它们一直保持在安全范围内。
5. 正确安装夹具和工件在进行加工任务之前，必须正确安装夹具和工件。
必须仔细检查夹具和工件的固定程度，以防止发生移动和脱落。
此外，必须注意夹具和工件所承受的力量和压力，确保它们不会超过它们的承受范围。
6. 注意防护栅和紧急停止装置高温高压声悬浮系统配备有防护栅和紧急停止装置，必须时刻关注它们的运转情况。
如果防护栅损坏或紧急停止装置失灵，必须立即停止操作，并进行修理或更换。
7. 结束操作和关闭设备在完成加工任务之后，必须先将设备的温度和压力恢复到正常水平，然后才能结束操作和关闭设备。
必须彻底清理设备、检查各部件是否有磨损和老化迹象，以便在下一次使用时及时处理。
流体悬浮床的应用与保养维护
流体悬浮床的应用与保养维护施翡翠;林玉丹【摘要】常见的流体悬浮床可分为两类:矽砂流体悬浮床和气流体悬浮床,我科现拥有五台矽砂流体悬浮床(以下简称悬浮床),数量居全国首位,流体悬浮床具有避免创面受压,降低感染、促进创面愈合、增加烧伤患者舒适度及减少护理工作等优点,是重度烧伤患者的救治重要辅助治疗手段,已经广泛应用于重症ICU及被迫卧床的患者[1].悬浮床的保养与维护关系到它的使用寿命及保养成本,如何做到有效低成本的保养维护,是使用医院关注的一大新问题.我们在使用悬浮床的十年里,总结出低成本有效保养的方法,在不影响悬浮床耗损的情况下,大大地减低成本,现总结如下:【期刊名称】《海南医学》【年(卷),期】2012(023)008【总页数】2页(P116-117)【关键词】流体悬浮床;工作原理;临床应用优点;保养维护【作者】施翡翠;林玉丹【作者单位】中国人民解放军第180医院烧伤整形科,福建泉州 362000;中国人民解放军第180医院烧伤整形科,福建泉州 362000【正文语种】中文【中图分类】R197.38常见的流体悬浮床可分为两类：矽砂流体悬浮床和气流体悬浮床，我科现拥有五台矽砂流体悬浮床(以下简称悬浮床)，数量居全国首位，流体悬浮床具有避免创面受压，降低感染、促进创面愈合、增加烧伤患者舒适度及减少护理工作等优点，是重度烧伤患者的救治重要辅助治疗手段，已经广泛应用于重症ICU及被迫卧床的患者[1]。
悬浮床的保养与维护关系到它的使用寿命及保养成本，如何做到有效低成本的保养维护，是使用医院关注的一大新问题。
我们在使用悬浮床的十年里，总结出低成本有效保养的方法，在不影响悬浮床耗损的情况下，大大地减低成本，现总结如下：1 悬浮床的构造与工作原理1.1 悬浮床构造以矽砂流体悬浮床为例，其结构主要由椭圆型大容器、纳米床板、可透气滤单、压气机、产热机、散热机、空气过滤器、滤水器，出入水排水管道、电脑控制板等部分零件组成。
医用悬浮床技术参数
医用悬浮床技术参数1.冷却方式：压缩机制冷。
2.分体式设计：设备由分体控制柜和悬浮床体两部分组成，应用区域和动力控制区域完全分离，彻底解决床体共振现象和噪音问题3.电磁兼容：可与其它大功率设备同时使用而不被电磁干扰4.床体工作方式：连续工作方式，间断工作方式，可根据患者实际情况选择5.床面离地高度：80cm，方便护理和换药，无须脚踏板，节省空间。
6. 信息管理：具有数据采集打印功能7. 散热器：纯铜材质散热器，耐高压、耐腐蚀、抗氧化，散热效能居各种材质之首；同时采用静音低功耗高风量散热风扇，散热性能优，散热风扇功率0.01KW*12,散热面积1.2平方米。
8.可调节靠背架：0°～60°之间任意调节角度。
9.移动性能：无水降温，不接水源，方便移动。
10.操作面板：10吋彩色液晶显示屏操作面板，显示界面：设备使用信息、运行状态信息、使用说明书、注意事项、维护保养知识、售后服务信息。
11.人体与床面接触压强降低：大于96% 。
12.悬浮力：变频自动调速功能，悬浮力无级可调，悬浮力大于246kg。
13.滤单：进口材质，抗张力强，兼备高密度、高透气性；孔径小于26um，确保颗粒不泄露。
14.微颗粒：500～560KG/每台，粒径：50μm～154μm；组织成分：陶瓷、有机硅复合材料（无毒、无味）。
15. 进口多孔板：木纤维密度低，透气性能均匀、良好，无任何化学粘合剂。
同时采用三排固定，受力分布均匀，坚固耐用。
16.噪声量：＜44dB17.重量：1、动力部分96kg；2、应用部分780kg（含微颗粒560kg)18.智能自检：具有故障自检功能、自动断电保护功能；配有过载保护装置，确保患者的人身安全。
悬浮床工艺流程范文
悬浮床工艺流程范文悬浮床（Floating Bed）是一种具有悬浮效果的床具，能够使人躺在床上感受到浮在空中的感觉。
下面是一个悬浮床的工艺流程，帮助你了解如何制造一个悬浮床。
1.设计悬浮床的尺寸和外观：首先，需要确定悬浮床的尺寸和形状，例如床的长度、宽度和高度等。
同时，还需考虑到床的外观设计，如使用什么样的材料、颜色和纹理等。
2.制作悬浮床的底座：悬浮床的底座是支撑整个床身的基础结构，通常由木材或金属材料制成。
根据设计要求，将木材或金属材料切割成所需的尺寸，并使用螺丝或胶水将各个部件连接起来。
3.设计和制作悬浮装置：悬浮床的特点在于能够使人感受到悬浮的效果，因此需要设计并制作相应的悬浮装置。
一种常见的悬浮装置是使用磁铁和电磁力来实现悬浮效果。
为此，需要购买和安装磁铁和电磁线圈，并将其固定在悬浮床的底部和床架上。
4.制作悬浮床的床身：床身是人们躺在上面的部分，一般由床垫和床架构成。
首先，根据设计要求，选购合适的床垫和床架材料，例如舒适的海绵材料或柔软的记忆棉等。
然后，根据床垫和床架的尺寸，裁剪相应的材料，并将其固定在床架上。
5.将床身连接到底座上：将床身顶部的床架与底座上的支撑结构连接起来。
使用螺丝、胶水或其他合适的连接件将两者固定在一起。
确保连接稳固，能够承受人的重量。
6.完善悬浮床的外观和舒适性：根据设计要求，对悬浮床的外观进行精细调整和修饰。
可以对床架进行喷漆、贴纹理等处理，使其更加美观。
同时，也可以添加舒适性增强的附件，如柔软的靠垫、羽绒被等。
7.测试和调整：在制作完成后，对悬浮床进行测试，确保其悬浮效果和舒适性符合设计要求。
如果有需要，进行相应的调整和修正，直至达到预期效果。
8.包装和交付：完成所有测试和调整后，对悬浮床进行包装，以防止在运输过程中受损。
然后，将悬浮床交付给客户或销售渠道，完成整个制造流程。
总结起来，制作一个悬浮床的工艺流程包括设计床的尺寸和外观、制作底座和悬浮装置、制作床身、连接床身和底座、完善外观和舒适性、测试和调整以及包装和交付。
悬浮床制作方案图
悬浮床制作方案图概述本文档将介绍一个悬浮床的制作方案图。
悬浮床是一种创新的家具，它使用悬浮技术将床体悬空，给人一种漂浮的感觉。
本文档提供了一个详细的制作方案图，帮助读者理解如何制作悬浮床。
材料清单在开始制作悬浮床之前，您需要准备以下材料：•床架材料：选择轻但坚固的材料，如铝合金或复合材料。
•悬浮系统：使用电磁悬浮或气压悬浮系统，确保床体能够悬浮。
•装饰材料：根据个人喜好选择适当的装饰材料，如木材、钢材或塑料材料。
•其它工具：工具包括电钻、螺丝刀、榫头机等。
制作步骤步骤一：设计床架首先，您需要设计一个合适的床架。
床架应该足够坚固，能够支撑住床体。
您可以使用CAD软件或纸笔绘制床架的设计图。
步骤二：准备悬浮系统根据您选择的悬浮系统类型，准备相应的材料和工具。
如果您选择电磁悬浮系统，您需要购买电磁悬浮装置和相应的电子元件。
如果您选择气压悬浮系统，您需要购买气压悬浮器和气泵。
步骤三：制作床架使用您准备好的床架材料以及相应的工具，开始制作床架。
根据床架的设计图，剪裁材料并按照图纸进行组装。
确保床架结实牢固，并能够容纳悬浮系统。
步骤四：安装悬浮系统根据悬浮系统的使用说明书，安装悬浮系统。
首先，您需要将悬浮装置或悬浮器安装在床架上。
然后，根据连接方式，将电子元件或气泵连接到悬浮装置或悬浮器上。
确保悬浮系统能够正常工作，并能够悬浮起床体。
步骤五：装饰床体根据个人喜好，选择适当的装饰材料装饰床体。
您可以使用木材、钢材或塑料材料等。
根据自己的实际情况，选择合适的装饰方法，如漆油、喷漆或镶嵌等。
步骤六：测试悬浮效果在床制作完成后，进行悬浮效果测试。
确保床体能够悬浮，并且稳定地保持悬浮状态。
如果出现任何问题，及时检查和修复。
结论本文档提供了一个悬浮床制作方案图，帮助读者理解如何制作悬浮床。
通过逐步的制作步骤，您可以根据自己的实际情况制作出一个漂浮的床体。
请注意，悬浮床的制作需要一定的技术和工具，并且需要保证床体的安全稳定。
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目录
一.工作原理
二.适应症
三.禁忌症
四.操作步骤
五.注意事项
六.终末处理
一.工作原理
分为沙粒悬浮床和空气搏动悬浮床.沙粒悬浮床内装入了600公斤由硅和陶瓷合成的细沙。
每粒沙直径只有50-150微米，细微得用肉眼看不见。
陶瓷粉、硅胶和碳酸钙粉等组成的特殊颗粒释放出的钠离子可使舱内的PH值维持在9-10左右，提供碱性环境，以减少细菌污染）充满流动舱，当经过过滤、加热后的压缩空气进入流动舱后，使微颗粒产生管状的自下而上的单一方向气泡流动效果，从而达到悬浮、按摩病人的作用，并吸附病人的渗出液。
吸附后的微颗粒，由于重力的原因而沉降到舱底。
如此循环反复，不但保证了特殊颗粒的流动，而且从根本上阻止了细菌的繁殖和交叉感染，从而有效地保证在工作状态下，局部的消毒环境。
该床还分别带有干燥功能，可以及时烘干伤员伤口的渗出液，避免感染和长褥疮。
悬浮床的应用大大缓解了烧伤病人的痛苦，也使创面愈合时间大大缩短。
二.适应症
1.大面积烧伤
2.躯干后侧或臀部烧伤
3.背/腰/臀慢性溃疡或压疮
4.手术后不宜搬动的病人
5.危重或者瘫痪患者
6.创伤后拌有骨折或脱位
三.禁忌症
1.体重超过150公斤
2.伴脊柱瘫痪的患者
四.操作步骤
1.启动悬浮床预热,至设定的温度(一般为30～36℃之间)
2.床体上铺设床单及烫单,以免渗液渗透
3.患者仰卧于悬浮床上,如有会阴部或者双上下肢烫者,应伸展四肢,呈”大”字型.
4.头面部肿胀者调节靠背垫,视情况调节高度
五.注意事项
1.由于悬浮床的构造特别，浮动的床面使患者本已存在的恐惧和疑虑心理加剧，使患者的心理更加脆弱，此时作为医务人员要理解病人的痛苦，要有高度的责任心和耐心向患者介绍该床的构造和治疗作用，并讲明此床本身是具有保暖作用的。
2. 床温的监测密切观察操作屏上的温度，如床温高于所设定的温度，需检查制冷系统运行是否正常及排水管道有无排水散热的现象;如床温低于设定的温度，需观察产热系统是否运行正常，排水是否停止。
3. 预防患者出现高渗性脱水悬浮床内持续干热气流使机体水分蒸发丢失增加，据估算可比正常水分丢失多2倍，从而使患者出现高渗性脱水。
卧悬浮床的患者，需鼓励多饮水，定期监测电解质，准确记录出入量，并根据其结果调整补液种类及补液量。
4. 病情观察密切观察患者的神志、精神状态、末梢循环及生命体征的变化，每小时监测1次生命体征的变化。
输液速度根据尿量及时调整，尿液一般维持在50～100ml/h。
气管切开者做好气道湿化，保持呼吸道通畅，防止肺部感染。
5．床温超过标定温度时会自动报警，此时须停机，可用空调或电扇以降低室温。
待床温降低后再重新启动。
六.终末处理
患者使用后用速消净对床单元进行全面的消毒；将滤单拆下用消毒液浸泡。
在悬浮状态下由两人配合提起格筛，弃去结晶颗粒。
每6个月清除1次筛网中的沙粒或异物、结晶等。