维德思说明书
【药品名称】
商品名称：维德思
通用名称：盐酸伐昔洛韦片
英文名称：Valaciclovir Hydrochloride Tablets
【成份】
盐酸伐昔洛韦
化学名称：L-缬氨酸-2-[（6-氧代-2-氨基-1，6-二氢- 9H -嘌呤-9-基）甲氧基]乙基酯盐酸盐。
分子式：C13H20N6O4·HCl
分子量：360.80
【性状】
薄膜衣片，除去薄膜衣后显白色或类白色。
【适应症】
1.主要用于带状疱疹。
2.用于治疗单纯疱疹病毒感染及预防复发，包括生殖器疱疹的初发和复发。
【用法用量】
成人·常规剂量·口服给药
1.单纯疱疹的治疗：一次500mg，一日2次。
对于单纯疱疹的复发，理想的服药时间为前驱期或症状及体征首
次出现时。
2.单纯疱疹的预防：(1)免疫功能正常的患者，一日给药总量为500mg，可分为1-2次给药。
(2)免疫缺陷的患者，服用剂量为一次500mg，一日2次。
3.带状疱疹的治疗：一次1000mg，一日3次，共7日，在发病的24小时内服用本药最有效。
【药理作用】
1.与齐多夫定（Zidovudine）合用可引起肾毒性，表现为深度昏睡和疲劳。
2.与丙磺舒竞争性抑制有机酸分泌。
【药代动力学】
口服后迅速吸收转化为阿昔洛韦，血中阿昔洛韦达峰时间为0.88～1.75小时。
口服生物利用度为67±13%，是
阿昔洛韦的3～5倍。
药物进入体内后广泛分布，可分布至多种组织中，其中胃、小肠、肾、肝、淋巴结和皮
肤组织中浓度最高，脑组织中的浓度最低。
药物在体内全部转化为阿昔洛韦，代谢物主要从尿中排除，其中阿昔洛韦占46%～59%，8-羟基-9-鸟嘌呤占25%～30%，9-羟基甲氧基鸟嘌呤占11%～12%。
阿昔洛韦原形为单相
消除，血消除半衰期（t1/2β）为2.86±0.39小时。
【药理毒理】
口服后吸收迅速并在体内很快转化为阿昔洛韦，其抗病毒作用为阿昔洛韦所发挥。
【注意事项】
1.交叉过敏对其它鸟嘌呤类抗病毒药(如阿昔洛韦、更昔洛韦、泛昔洛韦)过敏者也可对本药过敏。
2.禁忌症：(1)对本药或阿昔洛韦过敏者。
(2)孕妇。
(3)2岁以下儿童。
3.慎用：(1)肾功能不全者。
(2)脱水者。
(3)对免疫缺陷者不主张用。
4.药物对儿童的影响：2岁以下儿童禁用，2岁以上儿童慎用。
5.药物对妊娠的影响：动物实验未发现致畸性，但本药能通过胎盘，为安全起见，孕妇禁用。
美国药品和食品
管理局(FDA)对本药的妊娠安全性分级为B级。
6.药物对哺乳的影响：本药在乳汁中的浓度为血药浓度的0.6-4.1倍，哺乳妇女应慎用。
【不良反应】
1.消化系统少数患者有轻度胃肠道症状，如胃部不适、食欲减退、恶心、呕吐、腹痛、腹泻、便秘等。
2.中枢神经系统可出现头痛、乏力、眩晕。
3.血液可引起贫血、白细胞减少、粒细胞减少、血栓性血小板减少性紫癜(TTP)和溶血性尿毒症综合征。
4.心血管系统可引起心动过速、血管扩张等。
5.其它可见皮肤瘙痒、关节痛、肌痛、畏光、眼痛等。
【贮藏】
密封保存。
【规格】
0.5g。
SV4000系列双向热水和蒸汽双向阀说明书
JSV4000 Series 2-way hot water and steam solenoid valves are internally piloted. They feature brass and 316 stainless steel construction, and PTFE seal material. The temperature range of 0 to 182°C (32 to 360°F) and the PTFE O-ring make these valves ideal for media such as hot water and steam.A strain-relief connector is supplied with each unit. A ¹⁄₂" conduit plug is also available.SPECIFICATIONSMounting Position: Any (preferably with solenoid system upright)Maximum Process Temperature: 60 to 182°C (140 to 360°F) PTFE O-ring Maximum Ambient Temperature: Coil dependent (see ratings on coils)Voltage Tolerance: ±10% AC, ±5% DC Opening Time (ms):Approximately 100 to 200 Closing Time (ms): Approximately 200 to 1200Cycling Rate: Approximately 60 cpm Duty Cycle: Continuous (100%)Coil Molding Material:Black Polyphenylensulphide (Class H):SV8COIL-115/60 HZ SV8COIL-220/60 HZBlack Epoxy Resin (Class H): All 14 W coils, NEMA 4U N ormally Closed or Normally Open U I deal for Hot Water and SteamU 8 W, AC Coils Standard U 14 W, DC Coils Also AvailableOMEGA-FLO ®2-WAy HOt WAtEr And StEAM SOLEnOid VALVESSV4002A shownsmaller than actual size.SV4003A-NO shown smaller than actual size.SV4000A SeriesSV4003A-SS shown smaller than actual size.OMEGA-FLO ® 2-Way Hot Water and Steam Solenoid ValvesF EDBC AF EDAC BSV4002 (NO and NC)SV4002-SSACBF EDFE BCDADimensions for SV4003 and SV4004 (NO and NC)Dimensions for SV4003-SS and SV4004-SSJOrdering Examples: SV4002A , 1⁄2 NPT normally closed valve for 7⁄16" orifice. SV4004A-NO , 1 NPT normally open valve for 1"s orifice.Maximum operating pressure differential.shown smaller than actual size.。
Infiniti系列多参数生物反馈仪使用说明书
Infiniti系列多参数生物反馈仪使用说明书南京伟思医疗科技有限责任公司前言感谢您购买南京伟思医疗科技有限公司生产的生物反馈产品如果您是首次使用本设备，请您仔细阅读本手册，以便您更好的操作、使用本设备南京伟思医疗科技有限公司是国内知名的神经电生理检测设备的生产企业，公司生产的产品涵盖了临床电生理检测产品的所有领域，目前在国内三级甲等医院有大量的设备投入使用，本着更好的服务于客户的公司理念，为了帮助客户更好的使用本公司产品，更好的实现产品的功能，特制定本使用手册南京伟思医疗科技有限公司版权所有，任何组织、个人非经本公司授权不得传播、复制本技术手册，本手册解释权归南京伟思医疗科技有限公司。
本手册共分叁大部分注册产品标准 YZB/苏 0244——2008产品注册号苏食药监械（准）字 2008第2210236 号生产企业南京伟思医疗科技有限公司生产许可证苏食药监械生产许2003-0029号服务热线 025- 52442240 52442250 52442260 52442270 传真：025—2442230生产地址南京市江东中路303号奥体名座大厦E座11楼1104－1107室、F座11楼1105室注册地址南京市江东中路303号奥体名座大厦E座11楼1104－1107室邮编：210036目录第一篇Infiniti系列多参数生物反馈仪概述第一章系统使用简介 --------------------------------------------------------6第二章结构与技术特征 ---------------------------------------------------------7第三章设备的安装及调试 --------------------------------------------------------10第四章设备的维修与保养 --------------------------------------------------------12第五章传感器的放置 --------------------------------------------------------13第二篇 BioGraph Infiniti软件系统第一章启动程序---------------------------------------------151.1 生物反馈介绍 --------------------------------------------------------151.2 BioGraph Infiniti 软件 ------------------------------------------------------151.2.1 安装BioGraph Infiniti -------------------------------------------------------151.2.2 反馈程序快速启动 ------------------------------------------------------181.3 主菜单 ------------------------------------------------------------211.3.1 菜单操作-Menu Options ------------------------------------------------------211.3.2 退出程序 ------------------------------------------------------211.3.3 数据库备份 --------------------------------------------------------23第二章数据采集---------------------------------------------------232.1 说明 ---------------------------------------------------232.2 Script 训练 ---------------------------------------------------232.3 Open Display训练 ---------------------------------------------------232.4 界面选择 ---------------------------------------------------242.4.1设置界面的顺序 ---------------------------------------------------242.5 Script 训练方案 --------------------------------------------------24 2.5.1 Script 数据库 --------------------------------------------------25 2.5.2 Script编辑 --------------------------------------------------25 2.6 物理通道设置 --------------------------------------------------25 2.7 放大器检测错误 ---------------------------------------------------25 2.7.1 Infiniti 放大器DIP 开关 ---------------------------------------------------25 2.7.2 DIP开关设置 ---------------------------------------------------27 2.7.3 放大器生产序列号 ---------------------------------------------------27 2.7.4 编码器密码 ---------------------------------------------------28 2.7.5 应用程序密码 --------------------------------------------------28 2.8 电量状态 --------------------------------------------------28 2.9 传感器的连接 ---------------------------------------------------29 2.10 通道设置操作Channel Set -------------------------------------------------30 2.10.1 关于通道设置 ---------------------------------------------------30 2.10.2 通道设置操作 ---------------------------------------------------31 2.11 阻抗测试Impedance check ---------------------------------------------------322.12 基线调零Zeroing ---------------------------------------------------322.13编辑通道设置Edit Channel Set Settings---------------------------------------332.14 设置显示统计表Set Open Display Statistics -------------------------------------332.15主训练界面Main Frame Screen--------------------------------------342.16开始功能Open Display--------------------------------------372.17标准化训练方案Script Session Functions-------------------------------------372.18 当前动画列表Current Screen Instrument List- -------------------------------------402.19 开放式训练部分Open Display Session -------------------------------------412.20 域值About Thresholds-------------------------------------422.21 事件标志Event Markers --------------------------------------442.22视频工具Video Instruments -------------------------------------44第三章数据库Database-------------------------------------453.1 关于病人数据库About the Client Database -----------------------------453.2 主数据库Main Database -------------------------------------45 3.3 数据列表Database tables -------------------------------------45 3.4 训练部分Session Options -------------------------------------49第四章数据回放功能Review--------------------------------------524．1 关于回放功能About Reviewing Sessions -------------------------------------52 4．2 回放部分确认Review Session Confirmation -------------------------------------52 4．3 选择通道设置Select Channel Se -------------------------------------53 4．4 选择回放界面Select Review Screens -------------------------------------53 4．5 训练回放功能Session Review Functions ------------------------------------53 4．6 关于数据分析人工拒绝About Artifact Rejection--------------------------------------53 4．7 标志数据Artifacting data: --------------------------------------57 4．8 自动和手动筛选的说明 ------------------------------------58 4．9 浏览统计表Viewing Statistics ------------------------------------584.10 Script记录部分Recording a session ------------------------------------584.11 打印报告------------------------------------584．12 片段统计报告Segment Statistics Report -------------------------------------614．13关于趋势图报告About Trend Reports ------------------------------------614．14选择功能Select Sessions ------------------------------------614．15选择趋势报告Select Trend Report -----------------------------------624．16打印趋势图报告Printing a Trend Report ------------------------------------634．17使用训练趋势报告编辑器------------------------------------634．18趋势图报告编辑器------------------------------------64第五章闪存卡操作-----------------------------------655.1 关于闪卡操作-----------------------------------655.2 闪卡操作 Compact Flash Options ------------------------------------655.2.1 下载功能Download Session ------------------------------------655.2.2 选择通道设置Select Channel Set ------------------------------------665.2.3重建CF卡Rebuild Compact Flash ------------------------------------665.2.4创建Create ------------------------------------675.2.5. 更新Update ---------------------------------------------------675.2.6设置闪卡的时间Set Compact Flash Date/Time ----－---------------------------67第三篇 GSR2编码器的使用一、G SR 2如何工作――――――――――――――――――――――――――――69二、三种简单的放松训练―――――――――――――――――――――――――――69三、两种先进的想像训练―――――――――――――――――――――――――――70四、G SR 2对日常生活的益处――――――――――――――――――――――――――70五、G SR 2的维护―――――――――――――――――――――――――――――――71六、电池――――――――――――――――――――――――――――――――――71七、可选设备――――――――――――――――――――――――――――――――71第一篇 Infiniti系列多参数生物反馈仪概述第一章系统使用简介1.1 产品适用范围及注意事项1.1.1 产品适范围：焦虑症、儿童多动症等神经精神疾病的生物反馈治疗.1.1.2 不能检测心脏的纤颤。
德思XR06CX微型电子温控器（压缩机、融霜、蒸发器风扇控制）中文说明书
1. 目录1. 目录 _____________________________________________________________________________ 12. 注意事项 _________________________________________________________________________ 13. 概述 _____________________________________________________________________________ 14. 融霜 _____________________________________________________________________________ 15. 风扇 _____________________________________________________________________________ 16. 面板的键盘操作 __________________________________________________________________ 17. 参数 _____________________________________________________________________________ 28. 数字开关量输入 __________________________________________________________________ 29.安装与固定 ______________________________________________________________________ 2 10. 电气连接 _________________________________________________________________________ 2 11. 如何使用编程钥匙 ________________________________________________________________ 2 12. 报警信号 _________________________________________________________________________ 2 13. 技术参数 _________________________________________________________________________ 3 14. 接线图___________________________________________________________________________ 3 15.参数表及出厂设定值 ______________________________________________________________ 32. 注意事项∙ 请不要将温控器用于非下述目的以外的情况；不能作为安全保护设备使用。
DEL定量给料机说明书.
停
II:
Mfz
参数
:按此键显示POOX参数，X表示0〜7，
参數
1到P007参数后又从F008功能执行到F012功能，共十二个字代码，执行完从P000循环；
増加
3.1.3检查和改变设定参数的操作
确认
.,P001~ P007参数数值可修改，F008~ F012为功能键与确认键结合完成相应的功能.参数功能简介：
增加
P001
左移
确认
參数
-竝
移
例如：P001时，按增加键或左移键显示原零
点
增加可值为0123
假设现在改为0789,可按下列步骤完
成..0000;
::
……..0007;
瑜加
……..0070;
左移
……..0078;
璃加
……..0780;
确认
……..0789;
P000:置仪表地址，485通讯时用，详见通讯手册，操作步骤同上P001相同；P002:置仪表系数，操作步骤同上P001相同；
P003:置校零时间，操作步骤同上P001相同；
P004:置比例参数，操作步骤同上P001相同；
6
DEL定量给料机使用说明书
P005:置积分参数，操作步骤同上P001相同；
P006:置微分参数，操作步骤同上P001相同；。
Vitis AI用户指南说明书
Vitis AI 用户指南UG1414 (v1.4.1) 2021 年 10 月 29 日条款中英文版本如有歧义，概以英文版本为准。
赛灵思⽮志不渝地为员⼯、客户与合作伙伴打造有归属感的包容性环境。
为此，我们正从产品和相关宣传资料中删除⾮包容性语⾔。
我们已发起内部倡议，以删除任何排斥性语⾔或者可能固化历史偏⻅的语⾔，包括我们的软件和 IP 中嵌⼊的术语。
虽然在此期间，您仍可能在我们的旧产品中发现⾮包容性语⾔，但请确信，我们正致⼒于践⾏⾰新使命以期与不断演变的⾏业标准保持⼀致。
如需了解更多信息，请参阅此链接。
修订历史修订历史下表列出了本文档的修订历史。
目录修订历史 (2)第 1 章：Vitis AI 概述 (5)按设计进程浏览内容 (6)功能特性 (7)Vitis AI 工具概述 (7)Vitis AI 容器 (20)最低系统要求 (21)开发流程概述 (22)第 2 章：入门 (23)安装和设置 (23)运行示例 (33)支持 (37)第 3 章：量化模型 (38)概述 (38)Vitis AI 量化器流程 (39)TensorFlow 1.x 版本 (vai_q_tensorflow) (40)TensorFlow 2.x 版本 (vai_q_tensorflow2) (52)PyTorch 版本 (vai_q_pytorch) (63)Caffe 版本 (vai_q_caffe) (73)第 4 章：编译模型 (80)Vitis AI 编译器 (80)使用基于 XIR 的工具链执行编译 (81)VAI_C 用法 (100)第 5 章：部署和运行模型 (101)使用 VART 进行编程 (101)使用 VART 进行 DPU 调试 (102)多 FPGA 编程 (108)Apache TVM、Microsoft ONNX Runtime 和 TensorFlow Lite (109)第 6 章：模型剖析 (111)Vitis AI Profiler (111)第 7 章：模型最优化 (119)第 8 章：将 DPU 集成到定制平台内 (120)附录 A：VART 编程 API (121)C++ API (121)Python API (131)附录 B：附加资源与法律声明 (136)赛灵思资源 (136)Documentation Navigator 与设计中心 (136)参考资料 (136)请阅读：重要法律声明 (137)第 1 章Vitis AI 概述Vitis™ AI 开发环境可在赛灵思硬件平台上加速 AI 推断，包括边缘器件和 Alveo™加速器卡。
Manual de instrucciones de piscina说明书
Avda. Europa, 26 nave 3-4 P.I. l´estació - 17300 BLANES (Girona) Tel: 972. 33 23 11 - Fax: 972 35 25 06 - Servicio Asistencia técnica: 972.33 27 39e-mail:***********************MANUAL DE INSTRUCCIONES DEPISCINA •FUNCIONAMIENTO DEL EQUIPO DEPURADOR. •RECOMENDACIONES DE MANTENIMIENTO.FILTRACIÓN (FILTER).- Parar el motor.- Situar la maneta de la válvula selectora en la posición filtración (filter).- Abrir la llave de retorno (boquillas).- Abrir, hasta la mitad, la llave de fondo (sumidero).- Abrir la llave de skimmer(s) o deposito.- Cerrar llave de toma de limpiafondos.- Poner en marcha el motor.LAVADO DEL FILTRO (BACKWASH).Cuando la presión llegue a 1,3kg/cm2, lo cual indica que la arena filtrante no puede admitir más suciedad, se procederá a realizar un lavado del filtro de la siguiente forma:- Parar el motor.- Situar la maneta de la válvula selectora en la posición lavado (backwash).- Abrir llave de retorno (boquillas).- Abrir llave de fondo (sumidero).- Cerrar llave de skimmer(s).- Cerrar llave de toma de limpiafondos.-Poner en marcha el motor durante 2 minutos. Con esta operación se habrá vertido al desagüe toda la suciedad que obstruía el filtro.-Siempre, después de realizar un lavado del filtro, hay que realizar un enjuague del mismo.ENJUAGUE (RINSE).Con esta operación se vierte al desagüe el agua utilizada para el anterior lavado del filtro, de esta forma se evita que el agua turbia circule a la piscina. Esta operación se realizará siempre después de haber realizado un lavado del filtro.- Parar el motor.-Situar la maneta de la válvula selectora en la posición enjuague (rinse), -poner motor en marcha durante 30segundos.-Parar el motor.- Situar la maneta de la válvula selectora en la posición filtración (filter).RECIRCULACIÓN (RECIRC.)En esta posición la válvula selectora efectúa el paso del agua procedente de la bomba directamente a la piscina, sin pasar por el filtro. No suele utilizarse.VACIADO (WASTE).En esta posición se puede vaciar la piscina por medio de la bomba del filtro.Sólo se utilizarán en el caso de que la piscina no disponga de salida directa al desagüe.- Situar la maneta de la válvula selectora en la posición vaciado (waste). - Cerrar llave de skimmer(s).- Cerrar llave de toma de limpiafondos.- Abrir llave de fondo (sumidero).- Poner en marcha el motor.Para que la bomba aspire deberán mantenerse llenos de agua el prefiltro de la bomba y toda la conducción de agua del sumidero.No se deberá parar nunca el motor antes de que la piscina esté vacía. CERRADO (CLOSED).Se utiliza para cerrar el paso del agua del filtro a la bomba, para poder abrir el prefiltro del motor para coger el cesto recogecabellos.LIMPIAFONDOS MANUALPara pasar el limpiafondos manual a la piscina se realizarán estas operaciones:- Parar el motor.- Situar la maneta de la válvula selectora en la posición filtración (filter). - Cerrar llave de fondo.- Cerrar llave de skimmer(s).- Abrir llave de toma de limpiafondos.- Abrir llave de retorno.- Llenar de agua la manguera del limpiafondos, con objeto de expulsar el aire de la misma, y conectarla a la toma de limpiafondos.- Poner en marcha el motor.Después de pasar el limpiafondos se realizará siempre un lavado del filtro de la forma explicada anteriormente.LIMPIAFONDOS AUTOMÁTICOPara pasar el limpiafondos automático a la piscina, se realizarán las siguiente operaciones:- Parar el motor.- Situar la maneta de válvula selectora en la posición filtración (filter).- Cerrar llave de fondo.- Abrir llave de retorno.- Abrir llave de toma de limpiafondos.- Con la llave de skimmer(s) regular la presión del limpiafondos automático.- Llenar la manguera del limpiafondos de agua.- Poner motor en marcha.LIMPIEZA DEL PREFILTRO DEL MOTOR- Parar el motor.- Cerrar todas las llaves de la piscina.- Abrir tapa del prefiltro del motor y proceder a la limpieza de la cesta. - Una vez efectuada la limpieza, volver a situar las llaves en su posición.PUESTA A PUNTO DEL AGUAEL pHEl pH es la expresión de la acidez o alcalinidad de una solución. Los valores de pH están comprendidos entre 0 y 14, correspondiendo el valor 7 al grado neutro, los valores entre 0 y 7 a los grados de acidez yentre 7 y 14 a los grados de alcalinidad.Como norma general el pH del agua de una piscina debe estar comprendido entre 7,2 y 7,6.INCONVENIENTES DE UN PH DESESTABILIZADOUn pH demasiado bajo (ácido):Corrosión.Aguas turbias.Deterioro del vaso.Irritación de ojos, mucosas y piel.Disminución de la eficacia de los productos desinfectantes.Un pH demasiado alto (básico):Formación de incrustaciones.Decrecimiento de la eficacia desinfectante.Irritación de ojos.EL CLOROEn el agua, aún después de ser filtrada, existen bacterias que deben ser destruidas, por otra parte, las algas se forman con gran facilidaden aguas estancadas. Por esta razón será necesario la utilización dealgún producto bactericida con el fin de mantener el agua desinfectada. En este caso utilizaremos cloro, ya que es uno de los productos con más amplia aceptación.Las disposiciones sanitarias españolas vigentes determinan que el contenido de cloro residual libre en el agua de las piscinas debe estar comprendido entre 0,5 y 2 mg/l. (0,5 - 2 ppm.)。
8-1VisanteOCTUserManualChinese
用户手册Visante™ OCT■Model 1000Visante™ OCT 用户手册修订版控制部件号修订版软件版本说明发布日期60899-6 A 1.0Visante™ OCT 用户手册（中文）2006.01版权所有© Carl Zeiss Meditec Inc. 保留所有权利。
商标Visante™ 是 Carl Zeiss Meditec Inc. 的商标。
本文档中所有其它商标均为其各自所有者的财产。
目录目录(1)简介...................................................................................................1-1•使用说明..................................................................................................1-1•本用户手册的目的.................................................................................1-1• Visante OCT 技术......................................................................................1-2• Visante OCT 系统硬件.............................................................................1-3•警告：用户对软件或硬件的更改.......................................................1-4•仪器安装.................................................................................................1-4•避免损坏的窍门.....................................................................................1-4•嵌入的 Windows 许可证........................................................................1-5•产品遵从性.............................................................................................1-5•产品安全性.............................................................................................1-5•电磁兼容性 (EMC)...................................................................................1-6•附属设备.................................................................................................1-9•符号和标签............................................................................................1-10•仪器处置................................................................................................1-12•安装和使用可选的电源台...................................................................1-13 (2)操作概述...........................................................................................2-1•章节概述.................................................................................................2-1•启动和登录系统.....................................................................................2-1•初始系统设置.........................................................................................2-4•状态栏信息.............................................................................................2-8•操作模式和窗口.....................................................................................2-9•标题栏、菜单和工具栏......................................................................2-10•性能验证检查........................................................................................2-13•关闭系统电源........................................................................................2-16 (3)获取扫描...........................................................................................3-1•章节概述.................................................................................................3-1•准备患者.................................................................................................3-1•确定患者.................................................................................................3-2•选择检查程序.........................................................................................3-6•校准眼睛并获取扫描............................................................................3-7•查看扫描：保存或重试......................................................................3-11•获取之前的调整（可选）...................................................................3-15 (4)检查程序和扫描类型.......................................................................4-1•章节概述.................................................................................................4-1•检查程序.................................................................................................4-1• Exam Protocols 对话框............................................................................4-3•扫描类型.................................................................................................4-7目录(5)扫描分析...........................................................................................5-1•章节概述.................................................................................................5-1•访问分析.................................................................................................5-1• Analysis 窗口............................................................................................5-2•工具选项板.............................................................................................5-6•眼角膜厚度分析...................................................................................5-10•演示文稿导出........................................................................................5-13•打印.........................................................................................................5-15•示例报告................................................................................................5-15 (6)数据管理...........................................................................................6-1•章节概述.................................................................................................6-1• admin 用户...............................................................................................6-1•创建机构名称和徽标............................................................................6-1• Equipment（设备）：创建 Station Name（站名）............................6-3•人员登记.................................................................................................6-3•记录搜索.................................................................................................6-6•创建、编辑和删除患者记录.............................................................6-10•合并患者记录........................................................................................6-14•将患者记录分类....................................................................................6-16 (7)存档和检索.......................................................................................7-1•章节概述..................................................................................................7-1•患者数据库..............................................................................................7-1•数据维护要求.........................................................................................7-2•清除检查数据.........................................................................................7-2•存档建议.................................................................................................7-4•存档管理.................................................................................................7-5•手动存档.................................................................................................7-9•检索检查数据........................................................................................7-10 (8)例行维护...........................................................................................8-1•章节概述.................................................................................................8-1•更换保险丝.............................................................................................8-1•处理错误消息.........................................................................................8-4•硬盘碎片整理.........................................................................................8-5•例行清洁.................................................................................................8-5•用户更换部件列表................................................................................8-6(9)规格..................................................................................................9-1(10)法律声明..........................................................................................10-1•有限担保...............................................................................................10-1•服务合同...............................................................................................10-2•软件版权...............................................................................................10-2•软件许可证协议...................................................................................10-2目录附录 (A) 联网指导....................................................................................A-1•注意..........................................................................................................A-1•网络功能.................................................................................................A-1•警告：Internet 连接的风险...................................................................A-1•禁止的活动.............................................................................................A-2•不支持的网络活动................................................................................A-2•网络文件服务器最低要求....................................................................A-2•网络文件服务器建议............................................................................A-2•使用网络文件服务器............................................................................A-3•直接导出至个人计算机的配置...........................................................A-5附录 (B) 网络存储设备的配置.................................................................B-1•简介..........................................................................................................B-1• NAS 设备安全警告.................................................................................B-1• NAS 设备要求..........................................................................................B-1• NAS 设备建议..........................................................................................B-2•安装和配置 NAS 设备............................................................................B-2• NAS 设备清洁..........................................................................................B-5附录 (C) 打印机配置................................................................................C-1•简介..........................................................................................................C-1•打印机安全警告.....................................................................................C-1•认可的打印机.........................................................................................C-1•安装概述.................................................................................................C-2•点对点的无线配置................................................................................C-2•网络配置.................................................................................................C-6• USB 配置..................................................................................................C-7附录 (D) 测量数据....................................................................................D-1• Visante OCT 的精确性、重复性和再现性............................................D-1•眼角膜厚度数据....................................................................................D-2• LASIK 角膜瓣和基质数据.....................................................................D-4索引...................................................................................................I-1目录简介(1) 简介ZEISS Visante™ OCT Model 1000 (Visante™ OCT) 能够对眼前段进行详细的 in vivo 检查，而无需接触眼睛。
BOSCH Sicherheitssysteme GmbH(3)操作文件 2019版说明书
使用帮助 查找信息 打印帮助 简介 系统概述 硬件要求 软件要求 许可证要求 概念 BVMS设计理念 单个Management Server系统 Enterprise System Server Lookup Unmanaged site 自动网络补偿(ANR) 报警处理 兴趣区域(ROI) Intelligent Tracking 非活动注销 故障继电器 文本数据 脱机Operator Client 在脱机模式下进行工作 不指定版本的Operator Client 在兼容模式下工作 全景摄像机的查看模式 360度全景摄像机 - 适合安装在地板或天花板上 180度全景摄像机 - 适合安装在地板或天花板上 360度全景摄像机 - 适合安装在墙壁上 180度全景摄像机 - 适合安装在墙壁上 全景摄像机的裁剪视图 验证真实性 SSH数据通道 使用入门 启动 Operator Client 接受新配置 访问系统 使用 Server Lookup 显示摄像机图像 选择时区 在图像窗格中显示摄像机 显示全景摄像机 切换全景摄像机的查看模式 显示双重热成像/光学摄像机 显示多个 Management Server 的摄像机 在逻辑树中查找项目 更改图像窗格行数 排列图像窗格并调整其大小
使用联机帮助时，您可以随时从浏览器窗口中打印帮助主题和信息。 要打印帮助主题： 1. 右击右窗格，选择打印。
此时会打开打印对话框。 2. 单击打印。 P 主题会在指定的打印机上打印出来。
2019.08 | V 1 | Operator Client
操作手册
Bosch Sicherheitssysteme GmbH
2019.08 | V 1 | Operator Client
6 zh-CHS | 目录
14.3.5 14.4 14.4.1 14.4.2 14.4.3 14.4.4 15 15.1 15.2 15.3 15.4 15.5 15.6 15.7 15.8 15.9 15.10 15.11 15.12 15.13 15.14 15.14.1 15.14.2 15.14.3 15.14.4 15.15 15.16 15.17 15.18 15.19 15.20 15.21 15.22 15.23 15.24 15.25 15.26 15.27 15.28 15.29 15.30 15.31 15.32 15.33 15.34 15.35 15.36 15.37 15.38
WISE6000D-6S-2T使用说明书
WISE6000D-6S(M)-2T 工业以太网交换机使用手册（版本V1.0）烟台正维科技有限公司安全使用须知感谢您选择我公司的产品，我们将竭诚为您服务！本产品在设计使用范围内具有良好可靠的性能，但需要避免人为对设备造成的损害或破坏。
⏹仔细阅读本手册，并保存好本手册，以备将来参考用。
⏹不要将设备放置在接近水源或潮湿的地方。
⏹不要在电源电缆上放任何东西，应将其放在碰不到的地方。
⏹为避免引起火灾, 不要将电缆打结或包住。
⏹电源接头以及其它设备连接件应互相连接牢固，请经常检查。
⏹在下列情况下，请立即断开电源，并与我公司联系。
1、设备进水；2、设备摔坏；3、设备工作异常或展示的性能已完全改变；4、设备产生气味、烟雾或噪音。
⏹请注意保持光纤插座和插头的清洁。
设备工作时，不要直视光纤断面。
⏹请不要自己修理设备，除手册中有明确指示外。
物件清点请确认所购买的设备的包装盒是否完整，如果发现有任何配件短缺的情况，请尽快与我公司售后服务部联系。
我们会给您妥善解决。
1．打开包装箱，请注意包装箱方向，保证正面朝上。
2．取出装箱单、请按装箱单清点物件。
※【设备内置精密器件，请注意轻拿轻放，避免剧烈震动，以免影响设备性能】重要声明本用户手册中所提到的产品规格及相关资讯仅供参考，内容可能会有更新，恕不另行通知，如果需要部分详细说明请浏览正维网站： 或者直接与我公司售后服务部联系。
1.产品概述WISE6000D-6S(M)-2T系列产品是烟台正维科技有限公司专为煤矿设计生产的一款工业级低功耗八口光纤以太网交换机，支持2个10/100M电口和6个100M可光可电的接口，本产品所用器件经过严格筛选，主要元器件一律采用工业级器件。
电源输入方式选择了适合工业级标准的各类电源，增强了产品对恶劣及复杂环境的适应性。
2.产品特点高性能工业以太网交换机技术1. 高性能工业以太网交换技术2. 10/100BaseT(X)(RJ45),100BaseFX(SC,FC或ST接口,单模/多模)3. 支持IEEE802.3/802.3U/802.3X4. 存储和转发交换方式5. 10/100M,全/半双工,MDI/MDI-X自适应6. 提供背板交换容量1G7. 传输延迟小于6us8. 电口TVS(浪涌电压抑制)保护1KV的功能工业级别的高稳定性1. -45℃～80℃工作温度范围。
getinge assured - 产品册说明书
This document is intended to provide information to an international audience outside of the US.Getinge Assured Comprehensive range of indicators for wash monitoring and sterility assuranceAdded assurance - for clean and sterile goodsGetinge Assured indicators provide you with the added assurance that your equipment is cleanand sterile, as expected.Every day you reprocess a variety of instruments at different times, temperatures and conditions. You need reassurance that your sterile goods have been thoroughly cleaned and sterilized in accordance with your local standards and hospital requirements. Getinge is a world leader in cleaning, disinfection and sterilization equipment, with solutions for the healthcare and life science sectors. We understand that you need your disinfection and sterilization equipment to consistently perform to manufacturer’s specifications in full compliance with all requirements and standards.Getinge Consumables- The complete solutionThe Getinge Consumables offering is a comprehensive portfolio of products to support you in every step of your workflow. Getinge products conform to relevant standards, ensuring consistent and accurate quality of your results.Getinge CleanGetinge Clean is a complete detergent offering for global markets requiring enzymatic, alkaline or neutral cleaning solutions, suitable for both manual and automated processing. We offer specialized chemistry — such as pre-treatment foam to help keep instruments moist. We also offer rinse aid, lubricants, neutralizers and various descaling products including chamber foam as part of our maintenance offering. Getinge PackKeep your patients safe by using high-quality sterilization products. Even the most robust disinfection and sterilization processes can be rendered ineffective if the integrity of a medical pouch or its closure has been compromised during storage, handling, or transportation. That’s why Getinge Pack Sterilization Pouches and Rolls have been designed to provide an effective microbial barrier that significantly minimizes the risk ofrecontamination.Standard pouch Standard rollPouch made of Tyvek®Roll made of Tyvek®DuPont™ and Tyvek® are trademarks or registered trademarks of E.I. du Pont de Nemours and Company.Get accurate and consistent results - Every time, every dayImprove patient safetyYou can reduce the risk of hospital-acquired infections. GetingeAssured indicators are a relatively low-cost method of monitoringthe success or failure of the entire decontamination process. Thiswill help manifest itself in fewer cancelled operations, just-in-timedelivery of sterile instruments and contribute to the optimizationof the patient’s experience.Increase efficiency in your workflowOur training programs — available both face-to-face andelectronically — give you the tools you need to ensure consistentand accurate results for every point of your workflow. Our salestools and reference guides make it easy to interpret our products.All products come with clear pass/fail reference guides.Compliance with relevant international and localstandardsOur products give you complete peace of mind. Getinge Assuredproducts are all manufactured in ISO 9001 and ISO 13485 certifiedGetinge facilities and are tested against all relevant standardssuch as EN ISO 15883, EN ISO 11140 parts 1 & 4, and EN ISO 11138.We offer certificates of compliance for the complete range, aswell as 3rd party independent certificates for most products.Reduce environmental footprintGetinge Assured goes beyond wash monitoring and sterilityassurance. We also give you complete control in how you impactyour local environment. Our unique ink technology is non-toxicand contains no heavy metals in their base ingredients.Getinge AssuredWash MonitorGetinge AssuredWash Monitor F/RGetinge AssuredWash Monitor Ultrasonic Getinge AssuredWash Monitor U/LGetinge Assured ProteinTest Instrument SurfaceGetinge Assured ProteinTest Instrument LumenGetinge Assured ProteinTest Flexible Endoscope2,5 mGetinge Assured ProteinTest Dental Getinge Assured WashMonitor HolderGetinge Assured WashMonitor Holder FlexibleGetinge Assured WashMonitor Holder RigidGetinge AssuredTest Soil Wash Release Monitors- The first important step in sterile processingUsed routinely in washer-disinfectors or ultrasonic baths,our Getinge Assured Wash Monitors provide independentverification that the cleaning process is consistentlyproviding the desired result.As a final assurance of cleanliness, we offer a full range ofresidual protein tests for surfaces and instruments –including hollow lumens and endoscopes. With an instantprotein reaction, these tests are quick and easy to useand can detect residual protein down to 1 microgram inless than 10 seconds.Effective cleaning is the first important step in sterile processing. The best way to verify cleanliness is a reliable testing protocol that includes test soil, wash monitoring, and residual protein testing.Getinge Assured AdvaTec Bowie-Dick Test Pack 134˚C*Getinge Check Mini Bowie-Dick Pack 134˚C**Getinge Assured Bowie-Dick Test Pack 121˚C & 134˚C*Getinge Check Bowie-Dick Test Pack 134˚C**Getinge Assured Bowie-Dick Test Card TT Getinge Assured Bowie-Dick Test Card 134˚C Getinge Assured Bowie-Dick Test Sheet 134˚C* For use in Getinge GSS67H and HS66 Turbo Steam Sterilizers** For use in all sterilizers except Getinge GSS67H and HS66 Turbo Machine Release Monitors- Assurance of equipment performanceGetinge Assured Bowie-Dick tests monitor the effectiveair removal and steam penetration allowing you to releaseyour sterilizer for daily use. Getinge’s innovative Bowie-Dick type tests have been developed and tested toconform to the requirements of EN ISO 11140-4. With highly sensitive advanced ink, our technology provides greater accuracy and user information on process conditions compared to conventional test packs.The Bowie-Dick-type test remains the benchmark for daily testing of the mechanical function of your vacuum-assisted steam sterilizer.Getinge Assured Smart-Read Biological Test Pack Getinge Assured Self-Con-tained Biological Test PackGetinge Assured Smart-Well Incubator with PrinterGetinge AssuredMulti Incubator Getinge Assured Smart-ReadBiological Indicator (Steam)Getinge Assured Superfast20 Biological Indicator (Steam and VH2O2)Getinge Assured Batch Monitoring System 3.5, 4, 5.3 & 7Getinge Assured Helix Test 3.5, 4, 5.3, 7 & Formaldehyde Getinge Assured Self-Contained Biological Indicator (Steam, EO and VH2O2)Getinge Assured Express Incubator Getinge Assured 20 Superfast BiologicalIndicators for Steam and VH2O2 providesusers the assurance that the sterilizationload is safe to release in just 20 minutes.- Assurance of effective sterilization conditionsA chemical or biological process challenge device (PCD) gives the assurance that correct conditions have been achieved in the sterilizer chamber.Superfast 20 Biological Indicator (Steam)106 Geobacilus stearothermophilus 20 minutes Superfast 20 Biological Indicator (VH2O2)106 Geobacilus stearothermophilus 20 minutes Smart-Read Biological Indicator (Steam)105 Geobacilus stearothermophilus 10 hrs Fail; Cycle Verification: 3 to 5 hrs Self-Contained Biological Indicator (Steam)105 Geobacilus stearothermophilus 24 hours Self-Contained Biological Indicator (EO)106 Bacillus atropheaus 48 hours Self-Contained Biological Indicator (VH2O2)106 Geobacilus stearothermophilus 24 hoursGetinge Assured Emulating Indicators Getinge Assured Emulating Indicators, Adhesive Getinge Assured Integrating Indicator Getinge Assured MI Steam Migrating Integrator StripGetinge Assured Multicritical Process Variable Indicator (Steam)Getinge Assured Multicritical Process Variable Indicator (EO)Getinge Assured Multicritical Process Variable Indicator (Formaldehyde)Getinge Assured Multicritical Process Variable Indicator (VH 2O 2)Getinge Assured Green Tape (Steam) 18mm & 24mm Getinge Assured Record Labels for Steam, EO & VHP Getinge Assured Multicritical Process Variable Indicator (Dry Heat)- Sterility assurance at each instrument pack level When a pack is opened, OR staff can quickly verify sterilization conditions were achieved, and the pack is safe for use.3.5•4••5.3••7••18•Getinge Assured Emulating Indicators are the mostadvanced chemical indicators for monitoring the specificsteam sterilization parameters of time, temperature, andsteam inside the pack.Wash ReleaseTest Soil Washer-disinfectors504228300 Wash Monitoring and HoldersWash Monitor Wash Monitor Wash Monitor Washer-disinfectors503864500503864600503864700Wash Monitor F/R • Flexible & Rigid Washer-disinfectors6005500586Wash Monitor HolderWash Monitor Holder R • Rigid Lumen Wash Monitor Holder F • Flexible Lumen Washer-disinfectors / Ultrasonic6005500585503865000503865100Wash Monitoring, UltrasonicWash Monitor U • Ultrasonic Test Ultrasonic503865200 Wash Monitor U/L • Ultrasonic Test Ultrasonic6005500587 Protein TestsProtein Test Instrument SurfaceProtein Test Instrument Lumen Washer-disinfectors / Ultrasonic 503878500 503911200Protein Test Flexible Endoscope 2,5 m x 2,8 mmProtein Test Flexible Endoscope 2,5 m x 3,7 mm Protein Test Flexible Endoscope 2,5 m x 1,9 mm Protein Test Dental Washer-disinfectors / Ultrasonic503964400600550029660055002976005500000Machine ReleaseBowie-Dick TestsGetinge Assured Bowie-Dick Test Pack 134°C,Getinge Sterilizers Steam504052100Getinge Check Bowie-Dick Test Pack 134°C,Sub-trans cycles Steam6001154901 Bowie-Dick Test Pack 121°C Steam504052200 Bowie-Dick Test Card TT (Table Top Sterilizers)Steam6005500588 Bowie-Dick Test Card 134°C Steam6005500589 AdvaTec Bowie-Dick Test Pack, Getinge Sterilizers Steam504225100 Bowie-Dick Test Sheet 134°C Steam6005500590 Getinge Check Bowie-Dick Mini-Pack, Sub-trans Steam6001155600 Load ReleaseHelix TestsHelix Test 3.5Steam504052700Helix Test 4 Helix Test 5.3 Helix Test 7Steam504052800504052900504053000Helix Test Formaldehyde Formaldehyde504053100 Getinge Assured Batch Monitoring System PCDDevice Steam6005500575Batch Monitoring System Helix Test 3.5 (Refill Kit)Batch Monitoring System Helix Test 4 (Refill Kit) Batch Monitoring System Helix Test 5.3 (Refill Kit) Batch Monitoring System Helix Test 7 (Refill Kit)Steam6005500037600550003860055000396005500040Biological IndicatorsSuperfast 20 Biological Indicator Steam6005500506 Superfast 20 Biological Indicator VH2O26005500507 Express Incubator20 minutes6005500511Self-Contained Biological Indicator Self-Contained Biological Indicator Self-Contained Biological Indicator SteamEOVH2O25040539005040540006005500025Smart-Read Biological Indicator Steam504054100Smart-Read Biological Test PackSelf-Contained Biological Test Pack Steam 504054500 504054600Smart-Well Incubator with Printer10 hrs504054400 Multi Incubator24 hrs504054700 Pack ReleaseTapeGreen Tape 18 mmGreen Tape 24 mm Steam 6001154902 6001154903Record LabelsRecord Label Steam Record Label EO Record Label VHP SteamEOVH2O2600550040860055004096005500410Record Label Gun-6005500411 Type 4 IndicatorsMulticritical Process Variable Indicator Multicritical Process Variable Indicator Multicritical Process Variable Indicator L Multicritical Process Variable Indicator Multicritical Process Variable Indicator Multicritical Process Variable Indicator EOSteamSteamFormaldehydeDry HeatVH2O25040516005040517005040518005040519005040548006005500509Type 5 IndicatorsIntegrating IndicatorMI Steam Migrating Integrator Strip Steam 6005500594 6005500510Emulating Indicators - Non adhesiveEmulating Indicator 4Emulating Indicator 5.3 Emulating Indicator 7 Emulating Indicator 18Steam504051000504050800504050900504051400Emulating Indicators - AdhesiveEmulating Indicator 3.5 -AEmulating Indicator 4 - A Emulating Indicator 5.3 -A Emulating Indicator 7 -A Steam504051100504052600504051200504051300Miscellaneous.VH2O2 Indicator VH2O2504052000G E T I N G E A S S U R E D11With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 10,000 people worldwide and the products are sold in more than 135 countries.This document is intended to provide information to an international audience outside of the US.Getinge AB ·P.O.Box8861·40272Göteborg·Sweden·+46103350000·****************D M S -002438-r e v -f · 11/2022 · G e t i n g e i s a r e g i s t e r e d T r a d e m a r k · C o p y r i g h t b y G e t i n g e · S u b j e c t t o m o d i fi c a t i o n s d u e t o t e c h n i c a l d e v e l o p m e n t .。