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本標(biāo)準(zhǔn)規(guī)定了漢字鍵盤輸入用通用詞語。 本標(biāo)準(zhǔn)適用于漢字鍵盤輸入、方案優(yōu)化和評測。中文信息處理的其他領(lǐng)域也可參照執(zhí)行。
本標(biāo)準(zhǔn)規(guī)定了特殊制作或一般可得到的康復(fù)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(fù)輔助器具。下列術(shù)語不在本標(biāo)準(zhǔn)之內(nèi):——康復(fù)輔助器具的安裝所用的術(shù)語;——由本標(biāo)準(zhǔn)分類中的單個(gè)康復(fù)輔助器具組合的解決辦法;——藥品;——專用于保健的康復(fù)輔助器具和設(shè)備;——非技術(shù)解決辦法,比如他人輔助、導(dǎo)盲犬、唇讀法;——植入器;——財(cái)政支持。
本標(biāo)準(zhǔn)規(guī)定了電子商務(wù)交易中家用電器類產(chǎn)品信息的描述屬性與方法、模型、摘要描述以及擴(kuò)展方法。本標(biāo)準(zhǔn)適用于電子商務(wù)中家用電器類產(chǎn)品信息的發(fā)布、交換、存儲和管理等。
本標(biāo)準(zhǔn)給出了與納米技術(shù)相關(guān)的職業(yè)場所的健康和安全指南。本標(biāo)準(zhǔn)側(cè)重于納米材料職業(yè)制造和應(yīng)用相關(guān)的健康和安全條例。本標(biāo)準(zhǔn)提供的信息可以幫助相關(guān)公司、研究人員、勞動(dòng)者和其他人員在生產(chǎn)、操作、使用和處理納米材料時(shí)防止產(chǎn)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(yīng)用。本標(biāo)準(zhǔn)是基于目前能夠得到的關(guān)于納米技術(shù)的信息,包括表征、健康效應(yīng)、暴露評估和控制條例。
本規(guī)范適用于城鎮(zhèn)和農(nóng)村中小學(xué)校(含非完全小學(xué))的新建、改建和擴(kuò)建項(xiàng)目的規(guī)劃和工程設(shè)計(jì)。
本標(biāo)準(zhǔn)適用于綠色博覽建筑的評價(jià)。
本標(biāo)準(zhǔn)規(guī)定了汽車整車制造和汽車零部件及配件制造業(yè)中沖壓、車身、涂裝、總裝、動(dòng)力總成等五大制造工藝以及公用輔助設(shè)施所涉及職業(yè)病防護(hù)設(shè)施設(shè)計(jì)的具體內(nèi)容和要求,并給出了有關(guān)表述示例。本標(biāo)準(zhǔn)適用于上述汽車整車制造和汽車零部件及配件制造企業(yè)新建、擴(kuò)建、改建、技術(shù)改造和技術(shù)引進(jìn)項(xiàng)目,在初步設(shè)計(jì)(含基礎(chǔ)設(shè)計(jì)、實(shí)施方案、總體設(shè)計(jì)等)階段編制職業(yè)病防護(hù)設(shè)施設(shè)計(jì)專篇。其他汽車制造業(yè)建設(shè)項(xiàng)目可參照執(zhí)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 Elrical 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 sions of ANSI/RIA R15.06, for Industrial Robots and Robot Systems-Safety Requirements. Portions of the requirements in this have been excerpted from the Robotic Industries Associations (RIA) 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, inspion, 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 funons associated with the robotic application, not specifically addressed in this , shall also be evaluated to other applicable s/requirements. These may include, but are not limited to, Elrical Equipment for Laboratory Use; Part 1: General Requirements, 3101-1; Medical and Dental Equipment, 544; Power Operated Pumps for Petroleum Product Dispensing Systems, 79. In addition to the requirements in this , robots and robotic systems shall also comply with the applicable sions of the Elrical for Industrial Machinery, ANSI/NFPA 79. Robots and robotic systems intended for use in hazardous locations, as defined by the National Elrical 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, 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 .
This European 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; inspion 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 provides mechanisms through which various vendors of buildingautomation, control, and building management systems may exchange information in a ised way.This document provides specifications for the Application Elements of Control Network Protocol packets asfollows:Definitions definitions of ized packet (network-variable) data types;Definitions definitions of device-interface files;Definitions definitions of ized configuration-property types;Definitions definitions of ized enumeration types;Definitions definitions of ized funonal profiles;Definition definition of the ized 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 sor specific quality management system for healthcare. This 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 and can be used for certification of healthcare organizations. The requirements in this 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 also includes asps related to clinical risk management throughout the planning, operation and control of processes. This includes requirements for quality management but does not specify requirements for specific healthcare services. The quality management system requirements specified in this are complementary to requirements for healthcare products and services.