WEPERE ARYA Manuale utente
USER MANUAL
The good pressure for your sport.
3 USERMANUAL
TECHNICAL INFORMATION
MANUFACTURER 4
DECLARATIONOFCONFORMITY 4
CLASSIFICATIONS 5
INTENDEDPURPOSEAND SCOPE OF USE 5
DEVICEDESCRIPTION AND CONTROLS 6
TECHNICALSPECIFICATIONS 6
LABELLING 7
Packcontents 8
HOWTOUSETHEDEVICE
INTRODUCTIONTOTHETECHNOLOGY 9
CONTRAINDICATIONS 9
WARNINGS 9
USERPREPARATION 11
USEOFDEVICE 13
RECOMMENDEDTREATMENT SETTINGS 14
LOOKINGAFTER FOR THE DEVICE
MAINTENANCE 15
TROUBLESHOOTING 16
DISPOSALINFORMATION 17
WARRANTY 18
Support 19
Spareparts 19
INTERFERENCEANDELECTROMAGNETICCOMPATIBILITYTABLES 20
USERMANUAL 4
Manufacturer
I.A.C.E.R.S.r.l.
viaEnzoFerrari 2 • 30037Scorzè(VE) - Italy
Tel.041.5401356•Fax041.5402684
Declarationofconformity
Themanufacter: I.A.C.E.R.S.r.l
viaEnzoFerrari 2 - 30037Scorzè(VE) - Italy
declaresunderits ownresponsibilitythat theproduct
ARYA
Isconform tothe dispositionsofthe electromagnetic compatibilityDirective2014/30/UE of the
EuropeanParliament and ofthe Council ofthe 26thFebruary2014,to thecurrent TECHNICAL
STANDARDonELECTROMAGNETICCOMPATIBILITY EN60601-1-22015andthe followingrules
applied:
EN60601-12006+A12013,EN 60601-1-22015,EN 60601-1-62010+A12015,EN 60601-1-112015,
ENISO149712012,ISO10993-12018,ISO10993-52009,ISO 10993-10,EN 623662015.
Scorzè, 31/01/2022 MASSIMOMARCON
Place,date Legalrepresentative
5 USERMANUAL
Classifications
TheARYAdeviceassumesthe followingclassifications:
• ClassIIwithtype BF appliedpart(Classif.EN60601-1);
• IP21protectiondegreedevicein relation tothe penetrationof liquids and dust.
• deviceandapplicatorsnot subjecttosterilisation;
• devicenotsuitablefor use in thepresenceof a flammableanaestheticmixture withair or with
oxygen or with nitrousoxide;
• deviceintendedforcontinuous operation;
• devicenotsuitablefor externaluse.
Intendedpurposeandscopeofuse
TheARYAdeviceforintermittentpneumatic compressionisidealfor improving theperipheral
bloodandlymphaticcirculation. Thistype ofdeviceisdesigned for thefollowing applications:
• musclerecovery
• drainageofliquids
• improvementofthe blood andlymphaticcirculation
Thedevicecan be used byusersthemselves.Inthis casethey willalsoassumethe roleofopera-
torduring treatment.
Theminimumage for users tousethe device is18years.
USERMANUAL 6
Devicedescription and controls
Timer
Timesettingknob Pressure
Pressuresetting knob
Technicalspecifications
Feature Specification
Powersupply Mainspower supply 230VAC,50Hz
Fuses T1Ax1
Totalconsumption 100mAmax
Insulation(EN60601-1) II
Appliedparts (EN60601-1) BF
Dimensions(Lengthx Width xHeight) 260x200 x125 mm
Weight 2kg
IPprotection IP21
Pressure 200mmHg(±20%)
Treatmentduration 0÷ 30minutes
Operation Continuous
Conditionsofuse
Ambienttemperature From +5to +40°C
Relative humidity From15 to93%
Atmospheric pressure 700-1060hPa
Storage/transport conditions
Ambienttemperature From +5to +40°C
Relative humidity From15 to93%
Atmospheric pressure 700-1060hPa
Usefullife ofthedevice: 3years.
Brandlogo
Inaccordancewith Directive2014/30/EU.
Devicewith type BF applied part according to EN 60601-1ed.III.
ClassIIdevice
Manufacturerdata.
Dateofmanufacture(YYYY-MM).
Consulttheusermanual.
WEEEdirective for thedisposalofelectronic and electrical waste.
Serial number
IP21 Degreeofprotection against entry of solids, dusts and liquids (device
protected against solid foreign bodies with a diameter of ≥12.5mmand
againsttheverticalfallofwaterdrops).IP21
Caution,danger.
Allowedtemperatures(storagetemperatures,onpackaging)
Relative humidity(storagerelative humidity,onpackaging)
7 USERMANUAL
Labelling
SN
USERMANUAL 8
Packcontents
TheARYALEG2pack contains:
• no°1ARYAdevice;
• no°24 chambers leggings;
• no°14 chambers 8 terminations tube;
• no°2pressure plantars;
• no°1user manual;
• Non-wovenfabricstrip15x150 cm
Theconfiguration ARYALEG2isavailablein M orLoptions (ARYALEG2 M or ARYALEG2L).
Alsoavailableas optional itemsarethe legcuff extensions for widelegs.
N.B.:itis recommended to interpose the non-wovenfabricbandbetweenthefootand the
orthotic.
9 USERMANUAL
Introduction tothe technology
Intermittent pneumatic compression is a useful method for im-
provingperipheral blood and lymphatic circulation,reducingmu-
scle tension caused by stress or chronic and acute pain. Thanks
to its pump action, it promotes venous return (see figure below),
increasing the blood supply of the tissues and their consequent
correctphysiologicalrenewal.
Intermittent pneumatic compression is therefore able to solve
the problem of blood that could stagnate in damaged blood ves-
selsorin any case inareasofthe body thatarenotproperlysupplied.
Externalcompression also allowsexcessinterstitialfluids to return more easily to thecirculatory
system,sothat theycanbe properly and quickly eliminated.
Contraindications
Undesirableeffects may occur ifthe device isused in thefollowing situations orin people suffe-
ring fromthe followingdiseasesandconditions:
• peoplewith implantablemedicaldevices;
• peoplesufferingfrom pulmonaryoedema, heart attack,phlebocarcinoma,high blood
pressure,highfever;
• peoplesufferingfrom burns, dermatitis, purulent wounds, malignanttumours,etc.;
• peoplewhohaveundergone skinsurgery in thetreatmentarea;
• peoplewith severecirculation problems, such ashardeningof thearteries, angina,
heartattack, etc .;
• peoplewith suspected blood clots;
• peoplewith severemalformationsorwearersof prostheses(orotherfixationdevices)
inthe treatmentarea;
• immediatelyafterundergoingsurgery for thetreatment ofvaricose veins;
• userswhohave just undergone surgery,pregnantwomen,children;
CONSULTYOURDOCTORBEFORE STARTINGTREATMENTWITH THEDEVICE.
Warnings
Itisrecommended:
• to use the device keeping the applicator at least 3 metres away from televisions, monitors,
mobile phones or any other electronic equipment even if the device does not generate or
receiveany electromagnetic interference fromother equipment;
• to avoid use of the device by people who are not properly trained and who have not read
thismanual;
• during treatment, theuser is advisednot to wearmetalobjects;
USERMANUAL 10
• to pay attention to the use of connection cables in the presence of children/young people:
potentialstrangulationhazard.Keepoutofthe reach of children;
• positionthe devicesothat themains plug can beeasily disconnected;
• useONLYapplicatorssupplied by themanufacturer.
Itisforbidden:
• for the device to be used by people of unsound mind, who suffer from sensitivity disorders, or
temporarily unfit if not assisted by qualified personnel; children under the age of 12 or in any
casethose not adequatelytrained inthe use of the device by anadult;
• tousethedeviceifyoufindanydamageorsignsofdeteriorationtoitortotheapplicatorsand/
or cables: contact the retailer or the manufacturer as indicated in the Support paragraph.
Checkthe conditionofthe device beforeeachuse;
• to use the device near flammable substances, gases, explosives, in environments with high
oxygen concentrations,inthepresenceofaerosolsorinveryhumidenvironments(donotuse
inthe bathroomorwhileshowering/bathing);
• tousethedevicewhiledrivingvehiclesorwhileoperatingandcontrollingequipment/machinery;
• tousesharpobjects on thedevice.
Warning:
• itisforbiddentousethe deviceincombination withother devicesthat monitor/support
vitalfunctions.
• donotcrush,bendordamage theelectric cable. Electricalshockhazard.
• donotimmerse thedeviceinliquids.
• becarefulwhen closing theziptoavoid entangling hairorclothing.
• avoidknockingordropping thedevice.
• donotmovewhen you areusingthe device.
The manufacturer is to be considered responsible for the safety, reliability and performance of
thedevice provided that:
• anyadditions, modificationsand/orrepairsarecarriedout by authorised personnel;
• theelectricalsystemoftheenvironmentinwhichARYAisinsertedcomplieswithnationallaws;
• thedevices is usedinstrict compliance with theinstructions reported inthis manual.
Ifforeignsubstancesgetintothedevice,contacttheretailerormanufacturerimmediately.Should
the device fall, check that thereare nocracks inthe containeror damageof anykind; if thereare,
contactyour dealer ormanufacturer.
In the event of any change in performance during treatment, stop treatment immediately and
contactyour dealer ormanufacturer immediately.
Indice
