ANSI INCITS 256-2001 射频识别(RFID)(以前为ANSINCITS256-2001)

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【英文标准名称】:RadioFrequencyIdentification(RFID)(formerlyANSINCITS256-2001)
【原文标准名称】:射频识别(RFID)(以前为ANSINCITS256-2001)
【标准号】:ANSIINCITS256-2001
【标准状态】:作废
【国别】:美国
【发布日期】:
【实施或试行日期】:
【发布单位】:美国国家标准学会(ANSI)
【起草单位】:ANSI
【标准类型】:()
【标准水平】:()
【中文主题词】:
【英文主题词】:
【摘要】:EstablishesatechnicalstandardforafamilyofcompatibleRFIDdevices,specifically,RFIDdevicesoperatinginfreelyavailableinternationalfrequencybandsatlicense-freepowerlevels.Itspurposesareasfollow:PromoteinteroperabilityandcompatibilitybetweenRFIDdevicesbydefiningacommonAPIandlimitedphysicalanddatalinklayeroptions.Supportitemmanagementapplicationsandprovideflexibilityinthephysicallayerdefinitionstoallowadditionalfeaturesforusesthatvaluesuchenhancements.Thescopeincludesthefollowing:?Frequency?Interfacedefinitions?RDIDsystemdefinition?Minimumfeatures?Compliancerequirements?Documentstructureandreferences?Tagidentificationnumber?Manufacturer'stagidentificationnumber:MfrTagID?User'stagidentificationnumber:UserTagID
【中国标准分类号】:L71
【国际标准分类号】:
【页数】:
【正文语种】:英语


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Product Code:SAE AMS3814
Title:Cord, Coreless, Para-Aramid, Intermediate Modulus (Cancelled Feb 1996)
Issuing Committee:Ams P Polymeric Materials Committee
Scope: This specification has been 'CANCELLED' by the Aerospace Materials Division, SAE, as of February 1996.【英文标准名称】:Non-activesurgicalimplants-Particularrequirementsforcardiacandvascularimplants-Endovasculardevices
【原文标准名称】:非活性外科植入物.心脏和血管植入物的特殊要求.血管内植入物
【标准号】:BSEN12006-3-1999
【标准状态】:现行
【国别】:英国
【发布日期】:1999-03-15
【实施或试行日期】:1999-03-15
【发布单位】:英国标准学会(BSI)
【起草单位】:BSI
【标准类型】:()
【标准水平】:()
【中文主题词】:循环系统;设计计算;血管;灭菌;疲劳;设计;心脏病学;耐腐蚀性;腐蚀试验;修复术;力的测量;性能试验;医学专业;外科植入物;材料强度;文献索引;表面缺陷;疲劳试验;性能;尺寸;使用说明;外科设备;医疗设备
【英文主题词】:
【摘要】:ThisEuropeanStandardspecifiesparticularrequirementsforendovasculardevices.Withregardtosafety,thisstandardgives,inadditiontoENISO14630,requirementsforintendedperformance,designattributes,materials,designevaluation,manufacturing,sterilization,packagingandinformationsuppliedbythemanufacturer.NOTE1Vascularoccludersarenotaddressedinthisstandard.ForthetimebeingtherequirementsasstatedinENISO14630:1997applyfortheseproducts.NOTE2Duetothevariationsinthedesignoftheimplantscoveredbythisstandardandinsomecasesduetotherelativelyrecentdevelopmentofsomeoftheseimplants,acceptablestandardizedinvitrotestsandlongtermresultsofclinicaltrialsarenotalwaysavailable.Wherenotestmethodisdescribedinthisstandardacompletedescriptionofthevalidatedtestmethodandsamplepreparationprocedureusedshouldbedocumentedbythemanufacturer.Withregardtodesignevaluation,whereaspecificstandardizedtestisnotdescribed,guidanceisgivenbyreferringtocurrentscientificliterature(seeannexA).Thisstandardaimstoensurethatmanufacturerswilladdressallaspectsofdesignevaluationthatrelatetothesafetyoftheproduct.Asfurtherscientificandclinicaldatabecomeavailable,appropriaterevisionofthestandardwillbenecessary.
【中国标准分类号】:C35
【国际标准分类号】:11_040_40
【页数】:10P;A4
【正文语种】:英语