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电子秤技服手册一、秤的分类1、RL00－3600以太网联网方式（主板集成网卡）每台秤到 HUB的距离为100米2、RL00－3300以太网联网方式(非集成板)3、RL00－3100485联网方式，最多联64台，最远距离1000米。
4、RL00－3900单机版注：1）秤内程序和PC软件：3600秤内程序为149499.040，PC软件为以太网4.0；3300秤内程序为137487.020，用以太网2.0PC软件。
3100和3900相同，秤内为131741.042，PC软件用485联网的4.2版；二、符号说明：“*”表示确认“↓”表示下一步“↑”表示上一步1）plu(price lock up):特指某一商品，包含一系列商品信息如：商品号、货号、商品名称、组号、单价、税号、皮重号、计价方式、是否允许打折和是否允许改变单价等等。
2）PLU号（PLU NUMBER）：是秤内用于辨别不同商品的编号。
范围可以从1号至999999999999（13位）。
每一编号对应于店内的一种商品。
货号和PLU号的区别是：货号是给超市内的管理人员来区分不同商品的，而PLU号是给每一台秤来区分不同商品的。
也就是说，在同一商场内，不同的品种商品，在不同的秤内可能会是同样的PLU号，但其货号却应是不同的。
3）秤号（SCALE NUMBER）：在同一超市内，如使用多台条码秤，可使用秤号来区分不同的秤及其打印出的标签或收据。
秤号的范围可从1号到64号4）TLU（TEXT LOCK UP）：商品名称（COMMODITY NAME）5）预置键（PRESET KEY）：直接调用某一PLU的快捷按键。
6）包装日期（PACKAGE DATE）：也称为生产日期。
7）保质日期（SELL BY DATE）8）保质期（SELL BY OFFSET）9）以重计价类商品（BY WEIGHT PLU）10）以数计价类商品（BY COUNT PLU）11）固定重量（FIX WEIGHT）三、工作模式01、服务：前台操作02、预包装：后台配送03、代码：配置，编程，特殊功能，报表操作04、练习：练习销售08、大货物销售模式选择1）服务模式1. 按”模式”键2. 按“↓”键3. 按“*”键2）预包装模式1. 按”模式”键2. 输入“02”“*”键3. 按“↓”键四、打印纸种类0、收据1、标签五、标签格式1）标签格式标签格式共11种，1－3号可编程。
(19)中华人民共和国国家知识产权局(12)发明专利申请(10)申请公布号 (43)申请公布日 (21)申请号 201910938709.9(22)申请日 2019.09.30(71)申请人 梅特勒-托利多(常州)测量技术有限公司地址 213125 江苏省常州市新北区太湖西路111号申请人 梅特勒-托利多(常州)精密仪器有限公司 梅特勒-托利多国际贸易（上海）有限公司(72)发明人 朱顺康 胡万川 徐建飞 孙徐 扎伊德·萨伊德 (74)专利代理机构 上海专利商标事务所有限公司 31100代理人 陈亮(51)Int.Cl.G01G 21/02(2006.01)G01G 21/28(2006.01)(54)发明名称称重传感器组件及包括其的动态自动检重秤(57)摘要本发明提供了一种称重传感器组件及包括其的动态自动检重秤，所述称重传感器组件包括传感器上支撑板、分离式罩壳、称重传感器、传感器下支撑板和电机电缆，分离式罩壳的上端部与传感器上支撑板固定连接，分离式罩壳的下端部与传感器下支撑板固定连接，称重传感器固定在分离式罩壳内；称重传感器一端的上部与传感器上支撑板连接，另一端的下部与传感器下支撑板连接；电机电缆由分离式罩壳的上部穿入，下部穿出，且位于分离式罩壳内的电机电缆部分为分离式线缆，分离式线缆与称重传感器之间始终存在间隙且分离开来。
本发明称通过嵌入式的罩壳结构设计，降低外界粉尘、气流等环境因素对传感器的干扰，提升了传感器的防护等级。
权利要求书2页 说明书7页 附图8页CN 112577584 A 2021.03.30C N 112577584A1.一种称重传感器组件，其特征在于，所述称重传感器组件包括传感器上支撑板、分离式罩壳、称重传感器、传感器下支撑板和电机电缆，所述分离式罩壳的上端部与所述传感器上支撑板固定连接，所述分离式罩壳的下端部与所述传感器下支撑板固定连接，所述称重传感器固定在所述分离式罩壳内；所述称重传感器一端的上部与所述传感器上支撑板连接，另一端的下部与所述传感器下支撑板连接；所述电机电缆由所述分离式罩壳的上部穿入，下部穿出，且位于所述分离式罩壳内的所述电机电缆部分为分离式线缆，所述分离式线缆与所述称重传感器之间始终存在间隙且分离开来。
梅特勒—托利多RL00系列电子条码秤进阶设置详解一、IP地址设置:具体方法：按“代码/24681357/*/21/*〞，此时输入该秤的IP地址设置，如192.168.0.240，输入完毕后按“↓〞键，再输入子网掩码，如255.255.255.0，再按动“↓〞键，直到电子条码秤自动重新启动，设置完毕。
注：该设置可能因秤内软件版本的不同而不同，某些电子条码秤可能在设置完成IP后，需要手动重新启动〔即手动关机，再开机〕，视具体情况而定。
二、初始化:具体方法：按“代码/24681357/*/15/*〞此时选择：a)0=不进展初始化；b〕1=进展初始化按键选定后，按“*〞键，按“代码〞两次退出，完成设置。
警告:初始化以后所有数据都将被去除三、删除PLU数据:A)删除单个PLU数据：具体配置方法：“代码/1/*/08/*/需删除的商品的PLU号〞，按键选择：a)0=不删除；b)1=删除该PLU按键选定后，按“↓〞完成该PLU的删除，假设需继续删除其他PLU数据，那么录入需删除的PLU号，重复执行以上步骤，假设已删除完成那么按“代码〞键两次，返回正常状态。
B)删除所有PLU数据：〔该操作也可以在电子条码秤管理维护软件上执行〕具体配置方法：“代码/24681357/*/17/*〞，此时按键选：a)0=不删除；b〕1=删除所有PLU按键选定后，按“↓〞，再按“代码〞一次，完成删除，返回正常状态。
四、修改密码:设置密码：〔没有密码情况下〕具体配置方法：“代码/24681357/*/27/*/输入密码/↓/确认所输密码/↓/代码〞修改密码：〔已设密码情况下〕具体配置方法：“代码/输入旧密码/↓/24681357/*/27/*/输入新密码/↓/确认所输新密码/↓/代码〞五、商品总价圆整:具体配置方法：“代码/666666/*/02/*〞，此时按键选择：1)0=不舍；2〕1=四舍五入；3〕2=全进；4〕3=全舍；5〕4=1/4圆整按键选定后，按“↓〞，再按一次“代码〞，返回正常状态。
To ensure the future success of late -stage product development processes, itcontinuously strengthens its capabilities, and seeks to maximize the time it spendson the science through investment in emerging and state -of -the -art technologiesthat can reduce otherwise trivial manual labor. This mindset drove the productdevelopment team ’s search for an automated solutions preparation system that iscompliant with regulatory requirements in a GMP setting. For example, for themeasuring devices in the system the team needed to follow the requirementsstated in pharmacopeias (USP and Ph.Eur.). They recognized that the balances, pHprobes, conductivity probes, temperature sensors and volumetric glassware mustmeet the stringent requirements set by these pharmacopeias. In addition, it wasalso essential to comply with data integrity requirements set by the FDA ’s 21 CFRPart 11 and EU ’s Annex 11. The selected system needed to capture and log criticalaspects of record keeping such as audit trails, reports, recipe composition, userpermissions and dosing records.THE CHALLENGEA top 20 global pharmaceutical company with headquarters in Europe, has been inoperation for a century. With a mission of developing medicines and treatmentsfor endocrine diseases, this company helps people live better every day. In orderto speed the development of medicines and treatments to market, it has adopteda culture of innovation where implementing cutting edge technology isencouraged, embraced and expected. It was this innovation culture that spurredthe concept of moving a research automation system into the GMP environmentand improve the efficiency of laboratory personnel and operations there.ABOUT OUR CUSTOMER"The flexibility the solution has provided for just -in -time preparation is a major benefit."AUTOMATED PREPARATION OFREAGENT SOLUTIONS FOR GMP LABS Case StudyAT A GLANCEC. SchwartzProject ManagerLabMinds collaborated with aTop 20 Global Pharmaceutical company and madeenhancements to Revo thatevolved the research productinto a GMP compliant solution.C. Schwartz, Project ManagerTHE SOLUTIONAfter an extensive review of available solutions,they selected LabMinds® Revo®,the benchtop automated solution preparation system that enables companies to automate the reagent preparation bMinds,upon the customer’s request,decided to collaborate and make enhancements to Revo that would evolve the research product into a GMP compliant solution.The project was launched in May of2019and they set out to find a dedicated and innovative technical Project Manager to drive this project.Schwartz was assigned as Project Manager.Schwartz is a specialist in laboratory automation and has a strong track record of leading teams and driving transformation.He accepted the challenge in a large part due to the fact that he had previous exposure to the Revo system from the2016SLAS conference when Revo won the innovation award.He recognized the potential to transform Revo into a GMP compliant system and accepted the challenge.REAGENT SUPPLY SCENARIOSThe above graphic demonstrates the need and the options available for reagents in a lab.By using the Revo, just in time reagent solutions are achieved without using lab personnel time.FORMING A TEAMSchwartz formed a dedicated team comprised of subject matter experts including a chemistry specialist and cross functional experts from other departments.This team combined forces with LabMinds and worked to deliver an automated solution preparation system that complied with GMP requirements.They knew that it needed to deliver a solution that provided the consistent quality,traceability and documentation required in the regulated pharmaceutical industry.The team also sought to solve three main challenges: reducing the time lab technicians spent on preparing reagents to allow them to focus on the science; limiting solution overproduction; and eliminating risk associated with manual documentation processes.After 18 months of intense dedication, the team achieved a huge milestone and Revo was approved internally for use in its GMP laboratory. The system approval was earned through a series of rigorous data integrity process reviews and hardware upgrades. They were then able to tackle the challenges they set out to solve. Just a few months after the launch, the team on -boarded many of its recipes and is already seeing positive impact.SYSTEM APPROVAL“I appreciate the opportunity to work for a company that iswilling to implement cutting edge technology. We willreap many benefits moving forward,” commentedSchwartz, the Project Manager. “The flexibility the solutionhas provided for just -in -time preparation is a majorbenefit. We have already reduced solution overproduction costs and leveraged the Revo system toreallocate our reagent prep team from redundant tasks towork that helps increase the speed of productdevelopment.”"I appreciate the opportunity to work for a company that is willing to implement cutting edge technology that will reap many benefits moving forward."C. Schwartz Project ManagerPrior to the implementation of GMP Revo, three laboratory technicians spent an entire daypreparing reagents for the week. Upon review of recipes required, many were found tohave an organic component. To overcome a current system limitation, LabMindsdeveloped a workflow process where the Revo produces the aqueous portion of thesolution with instructions for the organic component addition printed on the label. Eventhough organic components are still added manually it was decided that the newfoundflexibility of automating the manual weighing, pH verification and data registration madethe process worthwhile. The system now allows the team to order the reagents via theWeb or mobile interface, and reduces the FTE time needed to fulfill monotonous,procedural laboratory tasks by 66%. This allows these key team members to focus on thedata analysis and scientific work needed to produce results from sample analysis.POSITIVE RESULTSThis lab technician team also used to ensure that they did not run out of reagents during the week by creating an extra supply. At expiry, extra solutions were thrown away. Now the team has implemented just -in -time inventory best practices and produce the exact quantities of the solutions they need. They know that they have increased flexibility, and if they need more solutions they do not have to stop analysis to create them. They can simply reorder via the easy Web interface, and the solution will be ready within an hour. This flexibility allows the team to reduce the amount of inventory needed each week.Prior to the implementation, the team manually tracked preparation data on paper to ensure they could obtain the necessary information for upcoming audits. Now, the team utilizes a QR code printed on the bottle label that contains all information describing the preparation and scans this data directly into the LIMS system where a record is created for each bottle.C. Schwartz and the Revo systemhttps:///labmindsinchttps:///labmindsinchttps:///company/labminds/“After 6 months in operation I get continued feedback from the users on how happy they are to be relieved from the tight planning of manual preparation they used to have. Even though organic components are still added manually it is by far overshadowed by the newfound flexibility in the fact that all manual weighing, pH verification and data registration are completely removed from the process.”C. SchwartzProject Manager© 2021 LabMinds. . All Rights Reserved. LabMinds and Revo are registered trademarks and the property of LabMinds.Unauthorized use is strictly prohibited.Scanning of QR code imports solutions data into LIMSCHALLENGESBENEFITS Reduce FTE time spent on preparing reagents Reagent prep FTE time decreased by 66%Limit solution waste Just -in -time inventory best practices reduced solutionoverproduction costsEliminate risk with manual documentationprocessesDocumentation completed with full transparency andregulatory compliance provides peace of mind All samples, solutions and controls are registered in the LIMS, and thisdata aligns with existing records to populate the documentation ofthe analysis and ensures audit readiness. This process not onlyreduces the chance of human error, but also frees up time for the labtechnicians to focus on other tasks. Our customer now has peace ofmind knowing that documentation is completed with fulltransparency and regulatory compliance.。
