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本標準規定了漢字鍵盤輸入用通用詞語。 本標準適用于漢字鍵盤輸入、方案優化和評測。中文信息處理的其他領域也可參照執行。
本標準規定了特殊制作或一般可得到的康復輔助器具的分類。本分類包括那些需要他人幫助操作的康復輔助器具。下列術語不在本標準之內:——康復輔助器具的安裝所用的術語;——由本標準分類中的單個康復輔助器具組合的解決辦法;——藥品;——專用于保健的康復輔助器具和設備;——非技術解決辦法,比如他人輔助、導盲犬、唇讀法;——植入器;——財政支持。
本標準規定了電子商務交易中家用電器類產品信息的描述屬性與方法、模型、摘要描述以及擴展方法。本標準適用于電子商務中家用電器類產品信息的發布、交換、存儲和管理等。
本標準給出了與納米技術相關的職業場所的健康和安全指南。本標準側重于納米材料職業制造和應用相關的健康和安全條例。本標準提供的信息可以幫助相關公司、研究人員、勞動者和其他人員在生產、操作、使用和處理納米材料時防止產生對健康和安全不利的后果。這些建議廣泛適用于一系列的納米材料及應用。本標準是基于目前能夠得到的關于納米技術的信息,包括表征、健康效應、暴露評估和控制條例。
本規范適用于城鎮和農村中小學校(含非完全小學)的新建、改建和擴建項目的規劃和工程設計。
本標準適用于綠色博覽建筑的評價。
本標準規定了汽車整車制造和汽車零部件及配件制造業中沖壓、車身、涂裝、總裝、動力總成等五大制造工藝以及公用輔助設施所涉及職業病防護設施設計的具體內容和要求,并給出了有關表述示例。本標準適用于上述汽車整車制造和汽車零部件及配件制造企業新建、擴建、改建、技術改造和技術引進項目,在初步設計(含基礎設計、實施方案、總體設計等)階段編制職業病防護設施設計專篇。其他汽車制造業建設項目可參照執行。
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.