WEPERE ARYA User manual
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.
11 USERMANUAL
Userpreparation
1. Select the appropriate applicator for the area being
treated.
1.1. Leg cuffs
1.1.1.Attach the connector relating to the tube with 8
endings (for using two leg cuffs) or the connector re-
latingto thetubewith 4endingsif using a singlelegcuff;
1.1.2. Put on the leg cuffs (or the single leg cuff) and close the zip up to the top, then close the
Velcrofastener;ifitisnecessarytoincreasethecircumferenceofthelegcuffs,addtheextenders
forlegcuffs availableonrequest;
1.1.3. Insertthepressure orthoticsatthe lowerendsof thelegcuffs, under the sole of the foot.
N.B.: it is recommended to cut the non-woven fabric band according to the shape of the
pressureorthotics and place it betweenthefootand the pressure orthotics.
1.1.4. Connect the tubes to the 4 inlets on each leg cuff, making sure to connect the longer tube
tothe topmost connector(darker in colour) onthe leg cuff (thigh).
ZIP
PRESSUREORTHOTICS
VELCRO
CONNECTION
INLETS
USERMANUAL 12
1.2.Armcuff
1.2.1. Putonthearmcuffandconnectthetubestotheinletsonthearmcuffitself,makingsureto
connect thelongertubetothe topmostconnector (darkerincolour) on thearm cuff;
1.2.2. After connectingthetubestothe armcuff,connectthe tubes tothe air outletconnectoron
themachine.
USINGEXTENSIONS
Theextensionsforthelegcuffsareanoptionalextrathatallowsyoutoincreasethesizeoftheleg
cuffs and can berequestedby thecustomeratanytime.
Forcorrectuse ofthelegcuffs, usethezipsonthelegcuffsandontheextensionstojointhetwo
elements,asshown in the figureabove.
13 USERMANUAL
1. Plugthe powercableintothe mainssocket.
2. Putontheapplicatorssuitableforthetreatmentyouintendtoperform and
connect therelative connectortothe devicebody.
3. Adjust the pressure: the pressure can be adjusted from 0 to 200mmHg (±
20%), i.e. the maximum pressure that can be set, by slowly turning the knob
clockwise.
4.
Adjustthetreatmenttime:thetreatmenttimecanbesetfrom0to30minutes.
WARNING!
Thedevicewill immediatelybegin delivering pressure into
thewornapplicators.
WARNING! Once the treatment has started, do not force the timer
byturning it anticlockwise.Waitfortheendof thetreatment to set the
desiredtime again.
5. Pressthe ON/OFFswitch on thedevicebody sothat it isON.
6. Attheendof the treatment press the ON/OFF switchOFF.
7. Ittakes about 2minutesfor theair to flow into the chambers insidethe ap-
plicators. Only when ALL the air has escaped from the chambers, unplug the
powercablefrom themains socket.
8. Disconnect theapplicatorconnectors fromthe device body.
9. Removethe tube connection inlets fromthe applicators.
10. Store the device and allitsapplicatorsin theirbox.
Useofdevice
Tousethe ARYAdevice:
USERMANUAL 14
Recommendedtreatmentsettings
If the 8-ending tube is used by connecting both leg cuffs, it is suggested to set the treatment
pressuresasfollows:
You should not excessively increase the pressure more the suggested values, in order to avoid
possibleinjuries.
Condition Pressure
(mmHg) Time(min) Recommended
applicator Treat-mentcycle
Drainageof liquids 50 30 Leg/Armcuff(s) 30days
Improvementof the bloodand
lymphaticcirculation 50 30 Leg/Arm cuff(s) 30 days
Musclere-covery 85 20 Legcuff(s) 30days
Condition Pressure
(mmHg) Time(min) Treat-mentcycle
Drainageof liquids 100 30 30 days
Improvementof the bloodand
lymphaticcirculation 100 30 30days
Musclerecovery 170 20 30days
15 USERMANUAL
Maintenance
Ifusedinaccordancewiththeinformationreportedherein,thisdevicerequiresnoparticularrou-
tinemaintenance operations.
Itisadvisable tocarryouta functionalcheck of thedevice at themanufacturer every24months.
The manufacturer does not consider the ARYA device to be repairable by personnel outside the
companyitself. Any operation inthis sense by personnel not authorised by the manufacturer will
beconsidered tampering with the device, thereby avoidingthe manufacturer’swarranty and fre-
eingitfrom liabilityforany hazards to whichthe operator or usermaybe subjected.
CLEANING
Si consiglia di spegnere ARYA alla fine di ogni seduta di trattamento, oltre a togliere i cavi dagli
appositiconnettori.
WARNING: device cleaning must not be performed while the device is in operation. Di-
sconnect the device from the mains, disconnect all connectioncables andperformclea-
ningwith thedevice switchedoff.
Useasoftdryclothtoremoveanydust fromthedevice.Incaseofhardtoremovedirt,useacloth
soakedinwaterand alcohol.
Tocleanthe cuffs,use a softcloth dampened ifnecessary,with asolution of water andalcohol.
Waituntilcompletely drybeforeusing the deviceandapplicators again.
Thedevicedoes not require sterilisation.
Notes:
• Neverusesolvents orchemicalsforcleaning. Cleaning agents candamagethe device.
• Carryoutroutine maintenance, inparticular:
•inspectthe bodyofthe device forcracksorfissures,whichmayallowliquids to enter;
•inspectthe cables.
Follow the above instructions only, for any other cleaning/maintenance operations contact the
manufacturer.
TRANSPORTANDSTORAGE
Transportprecautions
There is no particular care to be taken during transport as ARYA is a portable device. However, it
is recommended to put ARYA and the relative applicators in the holder supplied after each use.
Protect the device from intense heat, direct sunlight and liquids. Store the device in a cool and
well-ventilatedenvironment.
Donotplace heavyobjectsontopof thedevice.
USERMANUAL 16
Storageprecautions
Environmental operating conditions:
ambienttemperature from +5 to+40°C
relative humidity from15to 93%
pressure from 700to 1060 hPa
Environmental storage conditions:
ambienttemperature from +5 to+40°C
relative humidity from15to 93%
pressure from 700to 1060 hPa
Troubleshooting
Any type of work on ARYA must only be carried out by the manufacturer or authorised dealer. In
anycase,beforesendingARYAtothemanufacturer,itwillbenecessaryascertaintheexactnature
ofthe ARYAmalfunction.
Checkthe following:
Problem Solution
ARYAdoes notturnon 1. Checkthe connection tothemains.
2.Checkthepower ON/OFFbutton.
3. Checkthepower cableis notdamaged.
ARYAemits astrangehiss similarto leaking air
1. Checkfor damageand/or holesin thetubesand
connectors
2.Checktheapplicators arecorrectlyconnectedto the
device
3. Checkthatthe tubesarenot bentor squashed
Thereis nopressureor theairis notreaching
theapplicators
1. Checktheapplicatorconnectoris correctly connected
tothedevice
2.Checkthatthe tubesarenot bentor squashed
3. Checkthatthe airchambersinflaterhythmicallyand
gradually
Aircontinuesto enterthechambers and/oran
airleak isdetectedin the applicators Checkfor holesor damageinthe airchambers.If noair
leaksare found,turnoffthedevice, turn itbackon and
seeif itoperatescorrectly
Pressureistoo strongand/ortheuser feels
discomfort
1. Reducethepressure usingtheappropriateknob.
2.Turnoffthedevice anddetachthe applicatorsto
removeair from thechambers.
17 USERMANUAL
DisposalInformation
ARYA devices, in line with operating and safety requirements, have been designed and built to
have a minimum negative impact on the environment, following the provisions of the European
Directive2012/19/EUrelating to thedisposalof waste electricalandelectronicequipment.
Thecriteria followed are those of minimisingthe amount ofwaste,toxic materials,noise, unwan-
tedradiation and energyconsumption.
Carefulresearchintooptimisingmachineperformanceguaranteesasignificantreductionincon-
sumption,in accordance withthe subject of energysaving.
Thissymbolindicatesthatthisproductshouldnotbedisposedwithotherhouseholdwaste.
Correct disposal of obsolete equipment, applicators and especially batteries helps to
preventpossiblenegativeconsequencesonhumanhealth andthe environment.
The user must dispose of the equipment to be scrapped by taking it to the collection
centreindicatedfor thesubsequentrecyclingof electricalandelectronicequipment.
For more detailed information on the disposal of obsolete equipment, contact your local council,
wastedisposalservice orshopwhereyou purchased theproduct.
USERMANUAL 18
Warranty
IACER Srl guarantees a warranty period of 2 years from the purchasing date for ARYA device, un-
less information contained in this manual regarding installation, use and maintenance is stri-
ctly adhered. Thepartssubjecttowearandtear(pressureband)are excludedfrom thewarranty,
unlessthereareobviousmanufacturingdefects.Thewarrantywilllapseif:thedeviceismodified
inanywayor operated bystaff not authorised by themanufacturer orbythe authoriseddealer.
WARNING! In the event of non-shipment, the manufacturer declines all responsibility, if
corrective action on the equipment is necessary. Should you need to return the goods
then please pack the device and all the accessories so that it won’t be damaged during tran-
sportation. In order to be entitled to the warranty assistance, the purchaser must enclose to the
device a copy of the purchasing receipt, proving origin and purchasing date. For more informa-
tion on the warranty please contact the distributor or vendor, in order to check the norm and
standard in force in your Country, or ultimately the manufacturer IACER Srl.
Warrantyconditions
1) Shouldassistancebeneeded,enclosethepurchasingreceiptwhensendingthedevicetothe
manufacturer.
2) The warranty period is valid only on the electronic parts. The warranty will be granted by the
shopordirectly by themanufacturer.
3) Thewarranty coversonly theproduct damages, whichcausesits malfunctioning.
4) Warranty means that only the manufacturing defect components or material are covered by
reparationor freesubstitution, handwork included.
5) Warranty is not applied to damages caused by negligence or use not compliant to the given
instructions,byintervention onthe devicefrom personnelnotauthorized,accidentalcauses
ornegligenceformthepurchaser.
6) Warrantyisnotapplied in caseofdamagescaused by unsuitable powersupplies.
7) Warrantydoesnotapplytowearing parts.
8) Warrantydoesnotinclude transportationcostswhich have to becoveredby thepurchaser.
9) After the warranty period, the warranty is no more applicable. In this case all the assistance
interventions will be performed by debiting the costs of the substitution of the parts, the
handwork andthe transportationscosts.
10) ThecourtofVenicehas exclusivejurisdictionover any dispute.
19 USERMANUAL
Support
The manufacturer is the only point of contact for technical support regarding the device. For all
technicalsupportmatters, please contact:
I.A.C.E.R.S.r.l.
viaEnzoFerrari 2 • 30037Scorzè(VE) - Italy
Tel.041.5401356•Fax041.5402684
Technical documentation concerning repairable parts may be provided, but only with prior com-
panyauthorisationand onlyafter givingpropertraining to themaintenancepersonnel.
Spareparts
Original spare partsforthis device canbeordered at any timefromthemanufacturer. To order
themcontact:
I.A.C.E.R.S.r.l.
viaEnzoFerrari 2 • 30037Scorzè(VE) - Italy
Tel.041.5401356•Fax041.5402684
Use only original spare parts supplied by the manufacturer; if non-original spare parts are used,
theoperation andsafetyof theproduct might be affectedandthe warrantywill be nullandvoid.
USERMANUAL 20
Interferenceandelectromagnetic compatibility tables
The ARYA device is designed and built in compliance with the current TECHNICAL STANDARD on
ELECTROMAGNETICCOMPATIBILITY EN 60601-1-22015,with theaim of providing reasonable pro-
tection againstharmful interference inresidential, civil andhealthcare settings.
Basedontheiroperatingprinciple,thedevicesdonotgeneratesignificantradiofrequencyenergy
and have an adequate level of immunity to radiating electromagnetic fields. Under these condi-
tions,harmfulinterferencecannotoccurtoradioelectriccommunicationsandtotheoperationof
electro-medical devices used for monitoring, diagnosis, treatment and surgery, to the operation
of electronic office devices such as computers, printers, copiers, faxes, etc. and to any electrical
orelectronic appliance used in suchenvironments,providedthat theycomplywith theELECTRO-
MAGNETICCOMPATIBILITYdirective.
Inanycase,topreventanyproblemwithinterference,itisrecommendedtooperateanytreatment
deviceatan appropriate distant fromcriticalequipment for monitoring users’ vitalfunctionsand
to use caution in therapeutic applications on users with pacemakers. However, it is advisable to
use the device keeping a distance of at least 3 metres from televisions, monitors, mobile phones
oranyother electronic equipment.
Formoredetails see thecompatibility tables atthe end of themanual.
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