IEC 6060114 检查表 中英文版Word文档格式.docx
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601-1-4
TestReportFormNo.:
I601-1_C/97-04
TRFOriginator:
UnderwritersLaboratoriesInc.
MasterTRF:
dated97-04
Copyrightblanktestreport:
ThebodiesparticipatingintheCommitteeofCertificationBodies(CCB).ThisreportisbasedonablanktestreportthatwaspreparedbyKEMAusinginformationobtainedfromtheTRForiginator.
Testprocedure:
Testreportonly
Proceduredeviation:
N/A
Non-standardtestmethod:
Typeoftestobject:
Trademark:
Model/typereference:
Manufacturer:
Rating:
Copyofmarkingplate
GENERALINFORMATION
Testitemparticulars(seealsoclause5):
Classificationofinstallationanduse:
Transportableandportable
Supplyconnection:
Non-detachablecord
Accessoriesanddetachablespartsincludedintheevaluation:
---
Optionsincluded:
Possibletestcaseverdicts:
-testcasedoesnotapplytothetestobject:
-testobjectdoesmeettherequirement:
Yes
-testobjectdoesnotmeettherequirement:
No
Abbreviationsusedinthereport:
-normalcondition:
N.C.
-singlefaultcondition:
S.F.C.
-operationalinsulation:
OP
-basicinsulation:
BI
-basicinsulationbetweenpartsofoppositepolarity:
BOP
-supplementaryinsulation:
SI
-doubleinsulation:
DI
-reinforcedinsulation:
RI
Generalremarks:
"
ThisreportisnotvalidasaCBTestReportunlessappendedtoaCBTestCertificateissuedbyaNCB,inaccordancewithIECEE02"
.
(seeAttachment#)"
referstoadditionalinformationappendedtothereport.
(seeappendedtable)"
referstoatableappendedtothereport.
Throughoutthisreportapointisusedasthedecimalseparator.
Thetestsresultspresentedinthisreportrelateonlytotheobjecttested.
Thisreportshallnotbereproducedexceptinfullwithoutthewrittenapprovalofthetestinglaboratory.
Listoftestequipmentmustbekeptonfileandavailableforreview.
Summaryofcontentsprovidedonthelastpageofthisreport.
Generalproductinformationandconsiderations:
TheA&
J-POCB01OxygenConcentratorisintendedforuseasanoxygenconcentratortoprovidesupplementallowflowoxygentherapyinthehome,nursinghomes,patientcarefacilities,etc.TheA&
J-POCB01isavailablebyprescriptiononlyunderthesupervisionofaphysician,andisnotintendedtosupportorsustainlife.
SECTION
REQUIREMENT
Comment/Observation
Compliance(YES/NO/N/A)
6.
Identification,markinganddocuments
/
6.8
Accompanyingdocuments
6.8.201
AllrelevantinformationregardingsignificantRESIDUALRiskincludingdescriptionsoftheHAZARDSandanyactionsbytheOPERATORortheUSERnecessarytoavoid/mitigatethemshallbeplacedinboththeINSTRUCTIONSFORUSEandtheRISKMANAGEMENTFILE.
“UseManual”and“RiskManagementReport”includealltherelevantinformationregardingsignificantRESIDUALRiskincludingdescriptionsoftheHAZARDSandanyactionsbytheOPERATORortheUSERnecessarytoavoid/mitigatethem.
YES
6.8.202
ACCOMPANYINGDOCUMENTSforthePEMSshallidentify,asaminimum,theMANUFACTURERandauniqueidentifiersuchasrevisionlevelanddateofrelease/issue.
“UseManual””identifiestheMANUFACTURERandauniqueidentifiersuchasrevisionlevelanddateofrelease/issue.
52
Abnormaloperationandfaultconditions
52.201
Documentation
52.201.1
DocumentsproducedfromapplicationofthisstandardshallbemaintainedandTheprocedureforDeviceriskanalysisshallformpartofthequalityrecords;
seefigure201.Thisshouldbedoneinaccordancewith6.3ofISO9000-3.
Documentsproducedfromapplicationofthisstandardmaintainedaccordingto“DocumentManagementRequirementsofR&
DDepartment”andtheprocedureforDeviceriskanalysishasformedapartofthequalityrecordsinthe“RiskManagementReport”accordingto6.3ofISO9000-3
52.201.2
Thesedocuments,hereinreferredtoastheRISKMANAGEMENTFILE,shallbeapproved,issuedandchangedinaccordancewithaformalconfigurationmanagementsystem.Thisshouldbedoneinaccordancewith6.2ofISO9000-3
“NewProductDesignChangeRegulation”definesaformalconfigurationmanagementsystemfortheRISKMANAGEMENTFILEtobeapproved,issuedandchangedinaccordancewith6.2ofISO9000-3.
52.201.3
ARISKMANAGEMENTSUMMARYshallbedevelopedthroughouttheDEVELOPMENTLIFECYCLEaspartoftheRISKMANAGEMENTFILE.itshallcontain:
“RiskManagementReport”containsfollowings
a)identifiedHAZARDSandtheirinitiatingcauses
identifiedHAZARDSandtheirinitiatingcauses;
b)estimationofRISK;
hasanestimationofRISK;
c)referencetotheSAFETYmeasures,usedtoeliminateorcontroltheRISKoftheHAZARD;
GiveareferencetotheSAFETYmeasures,usedtoeliminateorcontroltheRISKoftheHAZARD.
d)evaluationofeffectivenessofRISKcontrol;
GiveanevaluationofeffectivenessofRISKcontrol.
e)referencetoVERIFICATION
Giveareferencetoverification.
52.202
RISKmanagementplan
52.202.1
TheMANUFACTURERshallprepareaRISKmanagementplan
“IntegratedDevelopmentPlan”hasbeenprepared.
52.202.2
Thisplanshallincludethefollowing:
a)scopeoftheplan,definingtheprojectorproductandtheDEVELOPMENTLIFE-CYCLEphasesforwhichtheplanisapplicable;
b)theDEVELOPMENTLIFE-CYCLEtobeapplied(see52.203),includingaVERIFICATIONplanandaVALIDATIONplan;
c)managementresponsibilitiesinaccordancewith4.1oflS09001;
d)RISKmanagementprocess;
e)Requirementsforreviews.
“IntegratedDevelopmentPlan”includesthefollowing:
e)Requirementsforreviews.
52.202.3
Iftheplanchangesduringthecourseofdevelopment,arecordofthe
changesshallbekept.ComplianceischeckedbyinspectionoftheRISKMANAGEMENTFILE.
IntegratedDevelopmentPlan”regulatesthatiftheplanchangesduringthecourseofdevelopment,therecordshallbekept.Andtheplandidnotchange.
52.203
DEVELOPMENTLIFE-CYCLE
52.203.1
ADEVELOPMENTLIFE-CYCLEshallbedefinedforthedesignanddevelopmentofthePEMS.
Dueto“IntegratedDevelopmentPlan”thedevelopmentlifecycleconsistsof:
-ProjectSchemeandEstablishmentphase;
-Requirementspecificationandanalysisphase;
-TechnicDesignphase;
-DevelopingPrototypemakeandVerificationphase;
-ProductVerificationandValidationphase;
52.203.2
TheDEVELOPMENTLIFE-CYCLEshallbedividedintophasesandtasks,withawell-definedinputoutputandactivityforeach.
Dueto“IntegratedDevelopmentPlan”
-ProjectSchemeandEstablishmentphase:
carryoutsurveyandresearchintermsofmarketandtechnologyandraiseapplicationforestablishingproject.
-Requirementspecificationandanalysisphase:
defineproductquality,performance,functionandappliedstandardsandregulationsandproductspecificationsbasedonintendeduses.
-TechnicDesignphase:
finishthetechnologydevelopmentandtestoftheproduct,andarchiverelevantdevelopmentdocuments.
-DevelopmentPrototypemakeandVerificationphase:
finishtheintegrationandverificationofthesubsystemandthewholemachine.
-ProductVerificationandValidationphase:
finishtheclinictestandconfirmthattheprototypedesigncomplieswiththeproductdesignrequirements,appliedregulationsandstandardsandthereforeitissafeandvalid.
52.203.3
TheDEVELOPMENTLIFE-CYCLEshallincludeintegralprocessesforRISKmanagement.
IntegratedDevelopmentPlan”definestheriskmanagementprocess.
52.203.4
TheDEVELOPMENTLIFE-CYCLEshallincludedocumentationrequirements.
IntegratedDevelopmentPlan”prescribestherequirementsforthedocumentswrittenduringeachphaseofthelifecycle.
52.203.5
RiskmanagementactivitiesshallapplythroughouttheDEVELOPMENTLIFE-CYCLEasappropriate;
see52.204.
Referenceto52.204.2
52.203.6
Whereappropriate,adefinedsystemforproblemresolutionwithinandbetweenallphasesandtasksoftheDEVELOPMENTLIFECYCLEshallbedevelopedandmaintainedasPartoftheRISKMANAGEMENTFILE,Dependingupontheproblem,thesystemmayhavethefollowingcharacteristics:
Thedocumentof“Riskmanagementreport”hasbeendefinedasasystem.Ithasthefollowingcharacteristics
bedefinedasapartoftheDEVELOPMENTLIFE-CYCLE;
beendefinedasapartoftheDEVELOPMENTLIFE-CYCLE
-allowthereportingofpotentialorexistingSAFETYand/orperformanceproblems;
allowthereportingofpotentialorexistingSAFETYand/orperformanceproblems
-includeanassessmentofeachproblemforassociatedRISKS;
includeaassessmentofeachproblemforassociatedRISKS
-identifythecriteria(SAFETYand/orperformance)thathavetobemetfortheissuetobeclosed;
identifiedthecriteria(SAFETYand/orperformance)thathavetobemetfortheissuetobeclosed
-identifytheactiontobetakentoresolveeachproblem;
identifiedeachactiontakentoresolveeachproblem;
-identifyVALIDATIONmethodsforeachaction;
identifiedVALIDATIO