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本标准规定了汉字键盘输入用通用词语。 本标准适用于汉字键盘输入、方案优化和评测。中文信息处理的其他领域也可参照执行。
本标准规定了特殊制作或一般可得到的康复辅助器具的分类。本分类包括那些需要他人帮助操作的康复辅助器具。下列术语不在本标准之内:——康复辅助器具的安装所用的术语;——由本标准分类中的单个康复辅助器具组合的解决办法;——药品;——专用于保健的康复辅助器具和设备;——非技术解决办法,比如他人辅助、导盲犬、唇读法;——植入器;——财政支持。
本标准规定了电子商务交易中家用电器类产品信息的描述属性与方法、模型、摘要描述以及扩展方法。本标准适用于电子商务中家用电器类产品信息的发布、交换、存储和管理等。
本标准给出了与纳米技术相关的职业场所的健康和安全指南。本标准侧重于纳米材料职业制造和应用相关的健康和安全条例。本标准提供的信息可以帮助相关公司、研究人员、劳动者和其他人员在生产、操作、使用和处理纳米材料时防止产生对健康和安全不利的后果。这些建议广泛适用于一系列的纳米材料及应用。本标准是基于目前能够得到的关于纳米技术的信息,包括表征、健康效应、暴露评估和控制条例。
本规范适用于城镇和农村中小学校(含非完全小学)的新建、改建和扩建项目的规划和工程设计。
本标准适用于绿色博览建筑的评价。
本标准规定了汽车整车制造和汽车零部件及配件制造业中冲压、车身、涂装、总装、动力总成等五大制造工艺以及公用辅助设施所涉及职业病防护设施设计的具体内容和要求,并给出了有关表述示例。本标准适用于上述汽车整车制造和汽车零部件及配件制造企业新建、扩建、改建、技术改造和技术引进项目,在初步设计(含基础设计、实施方案、总体设计等)阶段编制职业病防护设施设计专篇。其他汽车制造业建设项目可参照执行。
This Report provides a summary of the market analysis and forecast of the future market, as well as detailed data on the traffic forecasts, based on internal and external studies to the year 2010– 2020 as well as detailed data on the traffic forecasts in different parts of the world. It also provides examples of potential services and applicationsof future development of IMT-2000 and systems beyond IMT-2000 from the year 2010 onwards.
These requirements cover robots and robotic equipment rated 600 V or less and intended for installation in accordance with the National Electrical Code, ANSI/NFPA 70. Since end-use installation of a robot and robotic equipment may vary for each user application, guidelines for end-product installation may be evaluated to the applicable sections of ANSI/RIA R15.06, Standard for Industrial Robots and Robot Systems-Safety Requirements. Portions of the requirements in this Standard have been excerpted from the Robotic Industries Associations (RIA) Standard for Industrial Robots and Robot Systems - Safety Requirements, ANSI/RIA R15.06. These requirements cover robotic equipment and systems intended for indoor and outdoor use in applications such as parts assembly, parts transfer, automated material handling, inspection, loading, diecasting, deburring, welding, paint spraying, clinical/diagnostic systems, pharmaceutical applications, commercial food processing, automated vehicle refueling systems, library book handling/sorting, clean room applications, medical use for surgery, mobile robots, automated guided vehicles, automated storage/retrieval systems, and the like. Unique features or functions associated with the robotic application, not specifically addressed in this Standard, shall also be evaluated to other applicable Standards/requirements. These may include, but are not limited to, Electrical Equipment for Laboratory Use; Part 1: General Requirements, UL 3101-1; Medical and Dental Equipment, UL 544; Power Operated Pumps for Petroleum Product Dispensing Systems, UL 79. In addition to the requirements in this Standard, robots and robotic systems shall also comply with the applicable sections of the Electrical Standard for Industrial Machinery, ANSI/NFPA 79. Robots and robotic systems intended for use in hazardous locations, as defined by the National Electrical Code ANSI/NFPA 70, shall also comply with the requirements in Intrinsically Safe Apparatus and Associated Apparatus for Use in Class I, II, and III, Division 1, Hazardous (Classified) Locations, UL 913. In the following text, a requirement that applies to one type of equipment, such as a controller or teach pendant, will be identified by a specific reference. In the absence of a specific reference or if the term robot or robotic equipment is employed, it is to be understood that the requirement applies to all types of equipment covered by this Standard.
This European standard defines the field of packaging machines in detail, but briefly these are: Filling and Dosing machines; closing machines; labelling, decorating and coding machines; cleaning, sterilising, cooling and drying machines; fill and seal machines; inspection machines; container and component handling machines; form, fill and seal machines; cartoning machines; wrapping machines; group or transit packaging machines; pallet or loading unit forming, dismantling and securing machines.
This document European Standard provides mechanisms through which various vendors of buildingautomation, control, and building management systems may exchange information in a standardised way.This document provides specifications for the Application Elements of Control Network Protocol packets asfollows:Definitions definitions of standardized packet (network-variable) data types;Definitions definitions of device-interface files;Definitions definitions of standardized configuration-property types;Definitions definitions of standardized enumeration types;Definitions definitions of standardized functional profiles;Definition definition of the standardized method of file transfer between devices.The purpose of this specification is to insure interoperability between various CNP implementations. Thisdocument contains all the information necessary to read and interpret the format of data and controlinformation that is used by EN 14908-5. It also defines the device interface for a device as specified, which isnecessary to exchange data between various devices from different manufacturers.
This is a sector specific quality management system standard for healthcare. This standard incorporates EN ISO 9001:2015 and replaces EN 15224:2012 Health services - Quality management systems - Requirements based on EN ISO 9001:2008. This is a standalone standard and can be used for certification of healthcare organizations. The requirements in this standard comprehensively incorporate those from EN ISO 9001:2015 with additional requirements, specifications and interpretations for healthcare. Requirements have been added when considered relevant and existing clarified according to the specific healthcare context. This standard also includes aspects related to clinical risk management throughout the planning, operation and control of processes. This standard includes requirements for quality management but does not specify requirements for specific healthcare services. The quality management system requirements specified in this standard are complementary to requirements for healthcare products and services.