DeVilbiss DV51 Standard cpap series User manual

DV51 STANDARD CPAP SERIES
EN
DeVilbiss®IntelliPAP® Positive Airway Pressure Device
CAUTION–USA Federal law restricts this device to sale by, or on the order of a physician.
Assembled in USA of US & Imported Parts. Instruction Guide.
ES
Dispositivo de presión positiva en las vías respiratorias
IntelliPAP®de DeVilbiss®
PRECAUCIÓN–La ley federal de EE. UU. limita la venta de este dispositivo a médicos o a personas que dispongan
de la correspondiente orden médica.
Montaje efectuado en EE. UU. con piezas fabricadas en EE. UU. e importadas. Guía de instrucciones.
FR
Appareil de ventilation spontanée en pression positive IntelliPAP®
de DeVilbiss®
ATTENTION–En vertu de la loi fédérale américaine, cet appareil ne peut être vendu que par un médecin ou sur
ordonnance de ce dernier.
Assemblé aux États-Unis avec des pièces des États-Unis et des pièces importées. Guide d’instructions.

EN - 2
A
10 4
6
2
78
B
5 3
Key Features
1
2
6
4
3
5
7
C
2
3(bottom) 6
1
4
5
7
D
5
1
4
2
6
3(bottom)
7
E
1
2
DV51/DV5HH
DV5HH
1
5
2
6
3
7
4
8
910 11
F

EN - 3
EN ENGLISH................................................................................................ EN-3
ES ESPAÑOL ............................................................................................... ES-19
FR FRANÇAIS.............................................................................................. FR-36
TABLE OF CONTENTS
Symbol Definitions............................................................................................................................................... EN - 4
Important Safeguards.......................................................................................................................................... EN - 4
Introduction.......................................................................................................................................................... EN - 5
Intended Use ............................................................................................................................................. EN - 5
Indications for Use..................................................................................................................................... EN - 5
Contraindication......................................................................................................................................... EN - 5
Key Features....................................................................................................................................................... EN - 5
IntelliPAP Device ....................................................................................................................................... EN - 5
Keypad ...................................................................................................................................................... EN - 5
Humidifier Cradle....................................................................................................................................... EN - 5
Water Chamber ......................................................................................................................................... EN - 5
Therapy Management System .................................................................................................................. EN - 5
System Assembly................................................................................................................................................ EN - 5
Without Heated Humidification.................................................................................................................. EN - 5
With Heated Humidification....................................................................................................................... EN - 6
Keypad and Display ............................................................................................................................................ EN - 6
Operation............................................................................................................................................................. EN - 6
Start-Up ..................................................................................................................................................... EN - 6
Using the Comfort Delay Feature.............................................................................................................. EN - 6
Controlling the Humidity ............................................................................................................................ ER - 7
Shut Down................................................................................................................................................. EN - 7
Enable Menu List....................................................................................................................................... EN - 7
SmartCode®and Adherence Score Information........................................................................................ EN - 7
Patient Messages................................................................................................................................................ EN - 8
Reminders ................................................................................................................................................. EN - 8
Notifications............................................................................................................................................... EN - 8
IntelliPAP Travel Information ............................................................................................................................... EN - 8
IntelliPAP DC Operation ...................................................................................................................................... EN - 8
Battery Power............................................................................................................................................ EN - 8
Supplemental Oxygen......................................................................................................................................... EN - 9
Accessories/Replacement Items......................................................................................................................... EN - 9
Maintenance........................................................................................................................................................ EN - 10
Cleaning .............................................................................................................................................................. EN - 10
Troubleshooting................................................................................................................................................... EN - 11
Specifications ...................................................................................................................................................... EN - 12
Guidance and Manufacturer’s Declaration.......................................................................................................... EN - 14
Advanced Control Menus.................................................................................................................................... EN - 16

EN - 4
SYMBOL DEFINITIONS
Class II electrical protection-double insulated Type BF equipment-applied part
Data port input/output Standby-turns blower on/off
Next item on LCD display Increase value on LCD display
Previous item on LCD display Decrease value on LCD display
Attention, consult accompanying documents Heat
DC input: 12 VDC, center pin positive 100-240 VAC input 50/60 Hz
Locked Unlocked
IPX1 Drip-proof, vertical Delay-starts the delay cycle
This device contains electrical and/or electronic equipment that must be recycled per EC Directive 2002/96/
EC-Waste Electrical & Electronic Equipment
IMPORTANT SAFEGUARDS
READ ALL INSTRUCTIONS BEFORE USING
THIS DEVICE.
SAVE THESE INSTRUCTIONS.
DANGER
• ElectricShockHazard – Do not use while bathing.
• ElectricShockHazard – Do not immerse this device into water or any other liquid.
• ElectricShockHazard – Do not attempt to open or remove the cabinet. There are no user-serviceable internal
components. If service is required, return the product to your home care provider. Opening or tampering with the
product will void the warranty.
WARNING
• The DeVilbiss IntelliPAP should be used only with masks recommended by DeVilbiss, your physician or respiratory
therapist.
• To avoid rebreathing of exhaled air, do not use a CPAP mask unless the device is turned on and providing a supply
of air. Venting in the mask should never be blocked. When the device is turned on and providing a fresh supply of
air,exhaledairisushedoutofthemaskvent.However,whenthedeviceisnotoperating,exhaledairmaybe
rebreathed. Rebreathing of exhaled air for longer than several minutes can in some circumstances lead to
suffocation. This warning applies to most CPAP devices.
• The DeVilbiss IntelliPAP is not a life support device and may stop operating with certain device faults or with a power
failure. It is intended to be used on spontaneously breathing individuals weighing 66 lbs/30 Kg or greater.
• To avoid electric shock, always unplug power cord from wall outlet power source when performing cleaning.
• Use only accessories recommended by DeVilbiss.
• Alwaysremovethewaterchamberfromtheoptionalhumidiercradlebeforelling.
• Ifwaterhasspilledontothehumidiercradleorithasbeensubmergedintowater,unplugpowercordfrompower
source immediately. Allow device to dry completely before use.
• Neverblockairopeningsofthehumidiercradleorchamber.Donotinsertobjectsintoanyopeningsortubes.
• Forproperoperation,placesystemonaat,sturdy,levelsurface.
• Theoptionalhumidierisintendedforsingle-patientuseonly.
• Ifthesystemisplacedontheoor,donotpositionitwhereitmaybesteppedonwhengettingoutofbed.
CAUTION
• The circular data port connector located on the back of the IntelliPAP is used to attach accessories to the device.
The connector must only be used with accessories approved for use by DeVilbiss. Do not attempt to attach any other
device to this connector as it may damage the CPAP or the accessory device.

EN - 5
• Never rinse or place the device in water. Never allow liquids to get into or around any of the ports, switches or air
lter;doingsowillresultindevicedamage.Ifthisoccurs,discontinueuseandremovethepowercordfromthe
power source. Allow the device to completely dry before use.
• DonotplacetheIntelliPAPwhereitcanbeknockedontotheoororwherethepowercordmaycreateatriphazard.
• OnlytheDeVilbissDV5seriesHeatedHumidiersystemisrecommendedforusewiththeIntelliPAP.Other
humidiersystemsmaypreventthedevicefromdetectingsnoringandmaycauseinappropriatepressurelevelsin
the mask.
• Emptyanddryhumidierwaterchamberbeforetransporting.
INTRODUCTION
Intended Use
The DeVilbiss IntelliPAP Model DV51 Series Standard is intended for use in treating OSA in spontaneously breathing
patients 30 Kg (66 lbs) and above by means of application of positive air pressure. The device is to be used in home and
clinical environments.
Indications For Use (Optional Heated Humidifier)
Use on the advice and prescription of a licensed physician to help relieve the symptoms of dryness of the throat, nasal
passages and the mouth, which are common with positive airway pressure therapy. This is especially true in dry climates
and during the cold season when humidity in the air is typically lower than at other times.
Contraindication
Do not use IntelliPAP system if your upper airway has been bypassed.
NOTE–Symptoms of dryness of the throat, nasal passages, and the mouth are common with positive airway pressure
therapy. The IntelliPAP features an optional humidier system to help minimize these effects.
KEY FEATURES
DeVilbiss IntelliPAP Device (Figures A
and B)
1. Keypad/LCD Display (see Figure C)
2. Air Supply Port on Back
3. AirSupplyPortonBottom(foroptionalhumidier)
4. Air Supply Port Plug
5. HeaterPowerConnector(foroptionalhumidier)
6. AC Power Connector
7. DC Power Connector
8. Data Port
9. Power Cord (appropriate to your wall outlet) (not
shown)
10. Air Inlet Filter Opening
11 Connector Cover (not shown)
Keypad (Figure C)
1. On/Off
2. Previous Item
3. Next Item
4. Delay
5. Decrease Value
6. Increase Value
7. Heater PowerLED(foroptionalhumidier)
Ask your equipment provider for information about other
DeVilbiss masks, equipment, and accessories.
Humidifier Cradle (Figure D)
1. Heater Plate
2. Heater Power Connector
3. Storage Compartment for Connector Cover (on
bottom)
4. Air Supply Port Inlet
5. Air Supply Port Outlet
6. Flow Generator Release Button
7. Flow Generator Locking Tabs
Water Chamber (Figure E)
1. Chamber Lid
2. Chamber Base
3. Heat Transfer Plate (on bottom)
4. Sealing Gasket
5. Water Level Indicators (front and sides)
6. Chamber Release Latch
7. Chamber Disassembly Lever
Therapy Management System (Figure F)
1. SmartLink®(optional)
SYSTEM ASSEMBLY
Without Heated Humidification
1. Locate the air supply port and heater power connector on the bottom of the IntelliPAP device. Ensure that each
opening has the appropriate soft cover securely attached.
2. Place the IntelliPAP on a stable surface such as a nightstand or table. If you wish, you may also place the device on
theooratthebedside,beingcarefultoplacetheunitwhereitwon’tbekickedorsteppedon.Ensurethattheair
inlet in the back of the device is not blocked by anything such as curtains or bedding.
NOTE–Never place the IntelliPAP system on a soft surface such as a bed or couch during operation.

EN - 6
With Heated Humidification
CAUTION–The height of the IntelliPAP must be lower than the mask when using a humidier to prevent water from getting
into mask.
1. Ifyoursystemincludesahumidier,pleasefollowstepsinFigures1-7.
a. Remove the air supply tubing from the back of the device.
b. Locate the air supply port at the bottom of the device. Remove the port plug and insert it into the air supply
port in the back of the device.
c. Locate the heater power connector on the bottom of the device. Remove the connector cover and insert it into
thestorageopeninginthebottomofthehumidiercradle.
KEYPAD AND DISPLAY
Basic CPAP Controls
Name Symbol Function
ON/OFF TheON/OFFbuttonstartsandstopstheowofairfromthedevice.
HEATER 

IfyourIntelliPAPhasaheater/humidierattached,thesebuttonsadjusttheheatersetting.
Increase the setting for more humidity and decrease the setting for less humidity.
DELAY
The Delay button activates the comfort delay feature and only functions if this feature has been
enabled. To understand how to set the parameters of this feature, please refer to the Using the
Comfort Delay Feature found on page EN - 6.
NOTE– The left and right arrow keys on the control panel provide access to menus for specic settings. Ask your
homecare provider for more information.
OPERATION
1. Fully insert the power cord into the back of the device. Plug the other end of the power cord into the AC wall outlet.
2. Attach air supply tubing to air supply port in the back of the device.
3. Prepare the mask (supplied by your equipment provider) by referring to the mask’s instruction guide.
4. Connect the air supply tubing to the mask.
NOTE–The air supply tubing supplied with the device is specially designed to prevent kinking and allow you to receive
optimal airow. Use only the 22 mm diameter, smooth-bore, kink-resistant tubing supplied with this device or an air supply
tubing recommended by your equipment provider.
Start-up
Put on your mask and press the ON/OFF button on the keypad OR put on your CPAP mask and take a few breaths to turn
onairowautomatically.Thepressureinyourmaskwillrisetothesetpressureinabout10seconds.
NOTE–If the device does not automatically start after taking 2-3 breaths, this feature may have been disabled. If Auto ON/
OFF is disabled, you must manually press the ON/OFF button to start and stop the device.
The keypad display shows the actual mask pressure while the device is in use. Because this is the actual pressure, the
device pressure reading may vary slightly as you breathe.
IfyourDeVilbissIntelliPAPsystemincludesahumidier,itsheatercontrolsandstatusaredisplayed.
NOTE– If the display on your device is not similar to those listed above, refer to the section titled “Patient Messages” on
page EN-8.
Using the Comfort Delay Feature
YourIntelliPAPhasacomfortdelayfeaturetohelpmakeiteasierforyoutofallasleep.Theairowwillstartatalow
pressureandthengraduallyramp-uptotheprescribedsettingoverthelastfewminutesofthespecieddelaytime.
NOTE–When the delay comfort feature is activated, a message will ash on the display periodically, indicating the amount
of time remaining in the delay.
You can adjust the amount of time spent in comfort delay by using the advanced device controls. The Delay Time can be
adjusted from 0 to 45 minutes in 5-minute increments.
NOTE–If you are unable to change the delay time, your provider has locked this setting.
Pressthedelaybuttontoactivatethecomfortdelayfeature.Theairowpressurewilldroptotheprescribedcomfortdelay
pressure.

EN - 7
Inthenal10minutesofthedelayperiod,thepressurewillgentlyrisetothepressureprescribedforyourtherapy.You
mayrepeatthecomfortdelaybypressingthedelaybuttonagainifyouhavenotfallenasleepduringtherstuse.
Controlling the Humidity (optional)
The heater setting can be adjusted within a range of 1 to 10. The optimum temperature setting is dependent on the ambient
temperature and humidity of your room. If your room temperature is low and/or the relative humidity is high, then a lower
temperature setting may be necessary to prevent excess condensation in the air supply tubing. If the room temperature is
high and/or the relative humidity is low, then a higher temperature setting may be necessary for optimum comfort.
The heater setting of 1 results in a heater plate temperature of approximately 84°F (29°C). The heater setting of 10 results
in a heater plate temperature of approximately 149°F (65°C).
NOTE–Always allow at least 10 minutes of cooling time after turning the device off before removing the water chamber
from the humidier cradle.
WARNING
Donotattempttollthehumidierwhileitisattachedtothehumidiercradle.Damagetothehumidiercradle
mayoccur.
CAUTION–Use only distilled water that is at room temperature. Do not add any medication or other additives to the water.
CAUTION– For proper operation, ensure the ow generator is OFF before inserting humidier chamber.
WARNING
Nevertouchtheheaterplateonthehumidiercradle.Nevertouchtheheattransferplateonthebottomofthe
waterchamber.Theseplatescanreachtemperaturesashighas149°F(65°C)duringoperation.
Donotoperatetheheaterifthewaterchamberisempty.Theheaterplatemaybeturnedoffusingthekeypad
heatercontrolwhenbeingusedwithoutwater.
Shut Down
Press the ON/OFF button to turn the device off. You may also simply remove your mask. After a few seconds the device
willdisplaythemessage“MaskOff.Pleasecheckmaskt.”Ifyoudonotputthemaskonagainthedevicewill
automatically turn off in about 20 seconds. Pressing any button will remove the message from the display.
NOTE–If the DeVilbiss IntelliPAP does not turn off automatically, the Auto-OFF feature may have been disabled. In this
case you must manually turn the device off.
Enable Menu List
The Enable menu is available in all modes and is a sub-menu that allows you to control various functions of your IntelliPAP.
Itisaccessedbypressingthedownbuttonwhile“EnableMenu”isshownontheDisplay.
DisplayExample EnableMenuItemDescription
Auto-OFF 
Enabled
ThisoptioncontrolstheAuto-OFFfeature,whichautomaticallystopstheowofair
after taking off the mask. The device will require at least 30 seconds to turn OFF
depending on the kind of mask used. When Auto-OFF is enabled, Auto-ON is also
enabled. If the unlocked symbol is shown, you are able to adjust this setting. If the
locked symbol is shown, this setting can only be adjusted by your provider.
Auto-ON 
Enabled
ThisoptioncontrolstheAuto-ONfeature,whichautomaticallystartstheowofair
after breathing once or twice into the mask. This is always enabled when Auto-OFF is
enabled. If the unlocked symbol is shown, you are able to adjust this setting. If the
locked symbol is shown, this setting can only be adjusted by your provider.
LowBacklight
Enabled
Low backlight Enable will keep the backlight dim during operation. Low backlight
Disabled will turn the backlight OFF during operation.
ExitMenu
Press
Pressing the up key exits the Enable menu.
SmartCode and Adherence Score Information
Your homecare provider may contact you to retrieve SmartCode and Adherence Score information. To display the
SmartCode, press the LEFT arrow key once. Use the UP arrow or DOWN arrow keys to change the SmartCode reporting
period. Press the LEFT arrow key again to display the Adherence Score.

EN - 8
PATIENT MESSAGES
Your IntelliPAP will alert you of issues that may require some action on your part in order to make your therapy more
effective. You can press any key or button to clear the message from the display, but the IntelliPAP will operate normally
evenifthemessageisnotcleared.Twokindsofmessagesaredisplayed:RemindersandNotications.
Reminders
Reminders alert you when parts of your system need to be replaced. Some components of your system wear over time
and, if not replaced, may compromise your therapy. If you see a message on the display that is not listed below, you may
have the optional DeVilbiss SmartLink®Module attached to your device, which provides additional messages. Refer to the
documentation that was provided with the SmartLink Module.
CleanFilter–Theltershouldbecheckedevery10daysforsignsofdirtorwearsothatitcanbecleanedasneeded.
This message helps to remind you to check it regularly.
Notifications
NoticationsidentifyconditionsinyourIntelliPAPthatmayrequireactionbyyouoryourequipmentproviderinorderto
maintain a high level of therapy. If you see a message on the display that is not listed below, you may have the optional
DeVilbiss SmartLink Module attached to your device, which provides additional messages. Refer to the documentation that
was provided with the SmartLink Module.
DelayRunningxxMinutesLeft–Whileacomfortdelaysessionisactive,thismessageisashedonthedisplayevery5
seconds to let you know how much time is left in the delay.
MaskOff–Thismessageappearsduetoapoormasktoraremovedmask.Checkforleakaroundthemasksealand
make adjustments as necessary according to the mask manufacturer’s instructions. This message will be displayed until
thehighairowproblemiscorrected.Ifthehighairowconditionpersistsforabout20seconds,thedevicewill
automatically turn off if Auto-OFF is enabled.
DeviceFault – If a device fault message is displayed, refer to Troubleshooting for instructions.
INTELLIPAP TRAVEL INFORMATION
International Power Changes
Your DeVilbiss IntelliPAP is approved for sale and use in North America and is equipped with a universal power supply that
it is automatically capable of accepting line voltages of 100 to 240V~ 50/60Hz. You do not need to make any adjustments
to the device if you are traveling to another country where the line voltage is different than your domestic line voltage.
Simply contact your equipment provider for the correct style power cord for the region in which you will be traveling (refer
to Accessories/Replacement Items for the correct part number).
Altitude
Your IntelliPAP automatically compensates for changes in altitude between sea level and 9000 ft (2750 m). You do not
need to make adjustments to the device for changes in altitude.
INTELLIPAP DC OPERATION
Battery Power
Your IntelliPAP can be operated from a 12V DC power source in a motor home, boat or other recreational vehicle. The
power source can be used with a 12V DC power cord or a 12 V DC stand-alone battery. Both parts are available from your
equipment provider (refer to Accessories/Replacement Items for the correct part numbers). Both accessory cables are
required for stand-alone battery operation. The stand-alone battery connection uses clamps that attach to the terminal
connections of the battery.
NOTE–The heater for the IntelliPAP’s humidication system will not operate directly from a 12V DC power source. If you
need humidication, non-heated humidication is still available. Alternately, instead of connecting12V DC power directly to
the IntelliPAP, you can pass the DC power through an inverter that will deliver AC power to the system. This will allow the
heater to function. The power rating of the inverter must be at least 200 watts @ 110V~ / 400 watts @ 220V~.
NOTE–The IntelliPAP will automatically switch power sources between AC and 12V DC if both sources are available. If
your unit is connected to both AC and 12V DC power sources, it will operate on AC power as long as AC power is present,
and automatically switch to 12V DC power if AC power is lost. When AC power is restored, it will return to the AC source.
You do not need to reset or adjust any settings when the power source switches, but remember that your heater will not
operate on 12V DC.

EN - 9
SUPPLEMENTAL OXYGEN
WARNING-OXYGEN USE
• Oxygen supports combustion. To avoid possible physical injury, do not smoke while using this device with
supplementaloxygen.Donotusethisdevicenearhotobjects,volatilesubstancesorsourcesofopenames.
• Always turn on the IntelliPAP before turning on the oxygen source. Turn off the oxygen source before turning off the
IntelliPAP.
• Thisdeviceisnotsuitableforuseinthepresenceofaammableanestheticmixture.
• Ataxedowrateofsupplementaloxygen,theinhaledoxygenconcentrationwillvarydependingonthepressure
setting, patient breathing pattern, mask selection, and leak rate. This warning applies to most types of CPAP devices.
• Never allow the oxygen source to run continuously while connected to the IntelliPAP if the device is not in use. If the
IntelliPAPisnotbeingused,turnofftheoxygenow.
CAUTION
• Oxygen is a prescribed gas and should only be administered under the supervision of a physician.
• Theowsettingoftheoxygensourcemustbespeciedbyaphysician.
Supplemental oxygen is sometimes prescribed in addition to CPAP for treatment of Obstructive Sleep Apnea. If your
physician prescribed oxygen for your sleep therapy, you can add the oxygen in one of two ways:
1. Obtain the optional oxygen adapter (part #7353D-601) from your homecare provider and connect it to the air supply
port on the IntelliPAP. Connect one end of the air supply tubing to the open end of the adapter and the other end of the
air supply tubing to the mask.
2. If your mask is equipped with an oxygen port, your physician may request that you apply oxygen directly to your mask.
ACCESSORIES/REPLACEMENT ITEMS
Replacement Items
Air-inletlter(4/pk) DV51D-602 Heater connection cover DV51D-605
Fineparticlelter(4/pk) DV51D-603 Oxygen adapter 7353D-601
Air supply tubing (6’) DV51D-629 Carrying case DV51D-610
Air supply plug DV51D-604 HeatedHumidier DV5HH
HumidierChamber DV5C Chamber Sealing Gasket DV5C-614
Power Items
AC power cord (USA) DV51D-606 DC power cord DV51D-619
AC power cord (Brazil) DV51D-612 DC battery clamp-on adapter (requires DC
Power Cord DV51D-619) DV51D-696
DeVilbiss Masks RecommendedforusewithSleepCube
FlexSet®Masks Serenity®Masks
Large, Silicone 9354L Large, Silicone 9352L
Medium, Silicone 9354D Medium, Silicone 9352D
Small, Silicone 9354S Small, Silicone 9352S
Medium, Gel 9354G Medium, Gel 9352G
Small, Gel 9354GS Small, Gel 9352GS
Large, ComfortTouch™Silicone 9354LR Large, ComfortTouch Silicone 9352LR
Medium, ComfortTouch Silicone 9354DR Medium, ComfortTouch Silicone 9352DR
Small, ComfortTouch Silicone 9354SR Small, ComfortTouch Silicone 9352SR
Medium, ComfortTouch Gel 9354GR Medium, ComfortTouch Gel 9352GR
Small, ComfortTouch Gel 9354GSR Small, ComfortTouch Gel 9352GSR
EasyFit®Nasal Available in Silicone (S, M, L, XL), Gel (S, M, L) or SilkGel (S, M, L). Contact
your equipment provider
EasyFit Full Face Available in Silicone (S, M, L, XL), Gel (S, M, L) or SilkGel (S, M, L). Contact
your equipment provider

EN - 10
MAINTENANCE
DANGER
Electricshockhazard-Donotattempttoopenorremovethecabinet;therearenouser-serviceablecomponents
inside.Ifserviceisrequired,contactyourequipmentproviderforinstructionsonobtainingservice.Openingor
attemptingtoserviceyourdevicewillvoidthewarranty.
WARNING
Disconnectsupplybeforeservicing.
PressureAccuracy–The IntelliPAP is designed to provide accurate pressure performance from the factory without
additional calibration. No routine service is required provided the device is used in accordance with the manufacturer’s
directions.
NOTE–Some countries require periodic servicing and calibration of this kind of medical device. Contact your equipment
provider for further information.
StandardAir-InletFilter–Checkthelterevery10daysandcleanitifnecessary.Replacethelterevery6monthsor
soonerifitisdamaged.Thestandardlterisdesignedtolterparticleslargerthan3.0micronsinsize.TheIntelliPAP
MUSThavethestandardlterinplaceduringoperation.
OptionalFineParticleFilter–Checkthelterevery10daysandreplaceitifitisdirtyordamaged;otherwisereplacethe
lterevery30days.Theoptionalneparticlelterisdesignedtolterparticlesassmallas0.3micronsinsize.
CLEANING
WARNING
Toavoidelectricshock,alwaysunplugthepowercordfromthewalloutletpowersourcebeforecleaning.
CAUTION–Never rinse or place the device in water. Never allow liquids to get into or around any of the ports, switches or
air lter; doing so will result in product damage. If this occurs, do not use the device. Contact your equipment provider for
service.
Device Cabinet
1. Unplug the IntelliPAP from the power source. Wipe the cabinet with a clean, damp cloth every few days to keep the
cabinet dust free.
2. Allow the device to dry completely before plugging it into a power source.
Filters
Air-InletFilter
1. Theair-inletltershouldbecheckedevery10daysandcleanedasnecessary.Thelterislocatedintherearofthe
device.
CAUTION–Proper lter function is important for the operation of the device and to protect the device from damage.
2. Toclean,removethedarkouterfoamlterfromtheframe.
3. Washthelterinasolutionofwarmwateranddishwashingdetergent,andrinsewithwater.Allowtheltertodry
completely.Ifthelter(part#DV51D-602)isdamaged,contactyourequipmentproviderforareplacement.
4. Ensurethelteriscompletelydrybeforeinstallationanduse.
FineParticleFilter(Optional)
1. Ifyouhaveanoptionalneparticlelter(part#DV51D-603),inspectthislterandreplaceitifitshowssignsofdirtor
damage. Do not wash.
2. Installtheneparticlelterbehindthestandardlter.
NOTE–If the ne particle lter is not installed rst according to the directions, the life of the lter will be reduced requiring
more frequent replacement.
Optional Heated Humidifier
WaterChamber-Humidierwaterchambershouldbecleaneddaily.
1. Press on the chamber release latch and pull out the water chamber from the cradle (Fig 4).
2. Separate the chamber halves by pressing forward on the chamber disassembly lever and lifting the lid of the
chamber (Fig 9).
3. Remove the sealing gasket from the chamber lid (Fig 10).
4. Wash the parts in a solution of warm water and mild diswashing detergent.

EN - 11
CAUTION–Hand wash only. Do not use any solutions that contain bleach, chlorine, alcohol, scented oils or other aromatic-
based ingredients to clean the humidier components or tubing. These solutions may reduce the life of the product.
5. Allow the parts to dry before reassembly.
CAUTION–Inspect the gasket seal before each use to ensure that it is properly seated in the groove around the entire
chamber.
HumidierCradle-Thehumidiercradleshouldbecleanedasneeded.
1. Turn off the heater and unplug from power source. Allow system to cool for at least 10 minutes.
2. Detachowgeneratorfromthecradle;rstremovewaterchamberthenfullydepresstheowgeneratorrelease
button to separate (Fig 4).
NOTE–Flow generator release button must be pressed completely to separate.
3. Use a soft, damp cloth to clean the surfaces of unit.
Tubing
The air supply tubing should be cleaned daily. Remove the tubing from the device and mask. Use a mild detergent and
water to clean the inside of the tubing. Rinse the tubing and allow to air dry.
Mask and Headgear
Clean the mask and headgear according to the manufacturer’s instructions.
TROUBLESHOOTING
WARNING
ElectricShockHazard-Donotremovethedevicecabinet;therearenouser-serviceableinternalcomponents.The
cabinetshouldonlyberemovedbyaqualiedDeVilbissprovider.
Issue Possible Cause Remedy
Nothingshowson
thedisplay.
1. Device is not plugged in or the power cord
is not fully inserted.
1a.Verifythatpowercordisrmlyconnectedto
the IntelliPAP and the power outlet.
1b. If you are using a DC power source, make
sure the cable connections are secure. Verify that
battery is charged.
2.OptionalHumidier-Theowgeneratoris
notfullyseatedonhumidiercradle.
2. Refer to assembly instructions (Fig. 1-7).
3. There is no outlet power. 3. Locate a suitable functioning power source.
TheIntelliPAPdoes
notstartwhen
breathingintothe
mask.
1. The Auto-ON feature has been disabled. 1. Use the ON/OFF button to start and stop
device.
2. There is no power to the device. 2.Verifythatthepowercordisrmlyconnectedto
the device and the power outlet.
3. Breath is not deep enough for the Auto-ON
feature to detect.
3. Breathe deeply in and out to start the device.
4. You are using a full face mask that has an
anti-asphyxia valve.
4. Auto-ON may not work because your exhaled
breath escapes through the open valve. Use the
ON/OFF button to start and stop the device.
5. The air supply port plug is missing or not
fully inserted.
5. Make sure the air supply port plug is fully
inserted into the unit.
6.Thehumidierchamberisnotfullyengaged
into the cradle or is missing.
6.Slidethehumidierchamberfullyintotheslot.
Verify the latching lever snaps into place.
Theairowhas
stopped
unexpectedly
duringuseor
reportsmaskleak.
1. The Auto-OFF feature has detected large
airowbecauseoflooselyttingmask.
1.Ensureyouhaveagoodmaskt;adjustmask
and headgear.
2. During use, your mouth opens and you
begin to mouth-breathe.
2. Contact equipment provider for a chin strap or
different mask to prevent mouth-breathing.
3.Theoptionalhumidierchamberisnotfully
engaged or is missing.
3.Slidethehumidierchamberfullyintocradle.
Verify the release latch clicks into place.
4. The air supply port plug is missing from the
back of the CPAP or is not fully inserted.
4. Ensure the air supply port plug is fully inserted
into the back of the CPAP.

EN - 12
Issue Possible Cause Remedy
Thedisplayshows
adevicefault.
An error has occurred in the device and
requires servicing.
Contact your equipment provider for service.
Apneasymptoms
haverecurred.
1.Airltermaybedirty. 1.Cleanorreplacetheairlterandrelocate
device away from drapes or other dusty surfaces.
2. Apnea condition has changed. 2. Contact your physician or equipment provider.
Skinbecomes
irritatedwhere
maskcontactsface.
1. Headgear is too tight or improperly
adjusted.
1. Loosen headgear to reduce contact pressure
on face.
2. Your mask may not be sized properly or is
not the most appropriate shape for you.
2. Contact physician or equipment provider.
Drynessofthroator
nose.
Inadequate humidity. 1a.AddaDeVilbissDV5heatedhumidier.
1b.Increasetheheatersettingonthehumidier.
Watercondensation
collectinginthe
hosecausinga
gurglingsound.
1.Humidicationistoohigh. 1.Reducehumidierheatersetting.
2.Roomtemperatureuctuatesfromhigherto
lower levels through the night.
2. Increase room temperature.
Airfromow
generatorseemsto
betoowarm.
1.Airltersaredirty. 1.Cleanlters.
2. Air inlet port is blocked. 2. Unblock air inlet.
3. Room temperature is too high. 3. Lower room temperature.
4. Device is located near a heat source. 4. Locate device away from heat source.
5.Humidier(optional)heatersettingistoo
high.
5. Lower heater setting.
Nasal,sinusorear
pain,runnynose
Youmayhaveareactiontoairowpressure. Discontinue use and contact physician.
Heatersettingis
notvisibleon
display
1.Theowgeneratorisnotfullyseatedonto
thehumidiercradle.
1. Ensure proper contact is made (Fig. 3).
2. Your CPAP device is not equipped with the
optionalhumidier.
SPECIFICATIONS
CPAP
Size........................................................................................................... 4.2”Hx6.5”Wx6.9”D(10.7cm x 16.5cm x 17.5cm)
Weight ............................................................................................................................................................. 1.22 kg (2.7 lbs.)
Electrical Requirements AC......................................................................................................................100-240V~, 50/60 Hz
Electrical Requirements DC........................................................... .......................................................10.4 - 15 VDC, 5 Amps
Maximum Power Consumption ......................................................65 watts max from AC power source (flow generator only)
Pressure Range ......................................................................................................................................................3-20 cmH2O
Operating Temperature Range....................................................................................................... 41˚Fto104˚F(5˚Cto40˚C)
Operating Humidity Range.......................................................................................................0% to 95% RH non-condensing
Operating Atmospheric Conditions..........................................................................................Sea level to 9,000 feet (2743 m)
Storage & Transportation Temperature Range ..................................................................... -40°F to +158°F (-40°C to 70°C)
Storage & Transportation Humidity Range...............................................................................0% to 95% RH non-condensing
Maximum Limited Pressure...........................................................................................................20 cmH2O under normal use
Sound Pressure Level (tested per ISO 17510)...............................................................................................................26 dBA
Sound Power Level .........................................................................................................................................................38 dBA

EN - 13
Humidifier
Humidity Output (in the operating flow range): ................................................................................................ ≥10mgH2O/l air
Size:......................................................................................................2.6”Hx6.3”Wx8.4”D(6.6cmx16.0cmx21.3cm)
Weight: ........................................................................................................................................................1.75 lbs. (0.794 Kg)
Power Consumption:.................................................................................................................................................... 85 Watts
DV5HH Electrical Requirements ................................................................................................................100-240VAC, 0.95 A
Heater Plate Thermal Cutout:..............................................................................................................................305°F (152°C)
Power/Temperature Control: ......................................................................................Setting of 1 (minimum) to 10 (maximum)
Heater Plate Temperature: ...............................................................................84°F to 149°F (approx. 29°C to approx. 65°C)
Operating Temperature Range....................................................................................................... 41˚Fto104˚F(5˚Cto40˚C)
Operating Humidity Range.......................................................................................................0% to 95% RH non-condensing
Operating Atmospheric Pressure Range:........................................................................................................70.0 – 106.0 kPA
Filter Specifications
Standard Filter .........................................................................................................................................> 3.0 micron particles
Optional Fine Particle Filter .....................................................................................................................> 0.3 micron particles
Dynamic Short-Term Pressure Accuracy with and without DV5HH Humidifier (Per
ISO 17510-1:2007)
Waveform Volume[mL] BreathRate[min-1]
SetPressure
[cmH2O]
PressureAccuracy
[Pk-PkcmH2O]
Sinusoidal
cycle with I:E =
1:1
500 10, 15, 20
3.0 0.5
7.0 0.5
12.0 1.0
16.0 1.0
20.0 1.0
Maximum Flow-Rate (per ISO 17510-1:2007)
Test Pressures
3.0cmH2O7.0cmH2O12.0cmH2O16.0cmH2O20.0cmH2O
Measured pressure at the patient
connection port (cmH20) 2.1 6.0 11.0 15.0 19.0
Averageowatthepatientconnectionport
(l/min) 70.9 81.5 86.3 90.1 93.1
Pressure Swings (cmH2O peak to peak at 500ml tidal volume, sine wave profile)
Breathsperminute 10 15 20
 @6.5cmH2O0.5 0.5 0.5
 @10cmH2O1.0 1.0 1.0
 @13cmH2O1.0 1.0 1.0
 @20cmH2O1.0 1.0 1.0
Long Term Static Pressure Accuracy ................................................................................................................. +/- 0.5 cmH2O
Additional Specifications
Warranty.............................................................................................................................. Please contact homecare provider
Equipment classification with respect to protection from electric shock ........................................................................ Class II
Degree of protection from electric shock ................................................................................................. Type BF Applied Part
Degree of protection against ingress of liquids......................................................................................IPXI Drip-proof vertical
Mode of operation .................................................................................................................................................... Continuous
Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide

EN - 14
DEVILBISS GUIDANCE AND MANUFACTURER’S DECLARATION
WARNING
MedicalElectricalEquipmentneedsspecialprecautionsregardingEMCandneedstobeinstalledandputinto
serviceaccordingtotheElectromagneticCompatibility[EMC]informationprovidedintheaccompanying
documents.
PortableandMobileRFCommunicationsEquipmentcanaffectMedicalElectricalEquipment.
Theequipmentorsystemshouldnotbeusedadjacenttoorstackedwithotherequipmentandthatifadjacentor
stackeduseisnecessary,theequipmentorsystemshouldbeobservedtoverifynormaloperationinthe
congurationinwhichitwillbeused.
NOTE– The EMC tables and other guidelines provide information to the customer or user that is essential in determining
the suitability of the Equipment or System for the Electromagnetic Environment of use, and in managing the
Electromagnetic Environment of use to permit the Equipment or System to perform its intended use without disturbing
other Equipment and Systems or non-medical electrical equipment.
GuidanceandManufacturer’sDeclaration–EmissionsAllEquipmentandSystems
Thisdeviceisintendedforuseintheelectromagneticenvironmentspeciedbelow.Thecustomeroruserofthisdevice
should assure that it is used in such an environment.
EmissionsTest Compliance ElectromagneticEnforcement–Guidance
RF Emissions
CISPR 11 Group 1
This device uses RF energy only for its internal function. Therefore,
its RF emissions are very low and are not likely to cause any
interference in nearby electronic equipment.
RF Emissions
CISPR 11
Class B
Radiated and Conducted
Emissions This device is suitable for use in all establishments including
domestic, and those directly connected to the public low-voltage
power supply network that supplies buildings used for domestic
purposes.
Harmonics
IEC 61000-3-2 Class A
Flicker
IEC 61000-3-3 Complies
ImmunityTest IEC60601TestLevel ComplianceLevel ElectromagneticEnvironment-Guidance
Electrostatic
Discharge (ESD)
IEC 61000-4-2
±6kV contact
±8kV air
±6kV contact
±8kV air
Floors should be wood, concrete or ceramic
tile.Ifoorsaresynthetic,therelativehumidity
should be at least 30%.
Electrical Fast
Transient/burst
IEC 61000-4-4
±2kV on AC Mains ±2kV on AC Mains Mains power quality should be that of a typical
commercial or hospital environment.
Surge
IEC 61000-4-5
±1kV Differential
±2kV Common
±1kV Differential
±2kV Common
Mains power quality should be that of a typical
commercial or hospital environment.
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
>95% Dip for
0.5 Cycle
60% Dip for
5 Cycles
30% Dip for
25 Cycles
>95% Dip for
5 Seconds
>95% Dip for
0.5 Cycle
60% Dip for
5 Cycles
30% Dip for
25 Cycles
>95% Dip for
5 Seconds
Mains power quality should be that of a typical
commercial or hospital environment. If the user
of this device requires continued operation
during power mains interruptions, it is
recommended that the device be powered
from an uninterruptible power supply or
battery.

EN - 15
ImmunityTest IEC60601TestLevel ComplianceLevel ElectromagneticEnvironment-Guidance
Power Frequency
50/60Hz Magnetic
Field
IEC 61000-4-8
3A/m 3A/m
Powerfrequencymagneticeldsshouldbe
that of a typical location in a typical
commercial or hospital environment.
Conducted RF
IEC 61000-4-6
3 Vrms from
150 kHz to 80 MHz V1 = 3 Vrms
Portable and mobile RF communications
equipment should be separated from the
device by no less than the recommended
separation distances calculated/listed below:
D=(3.5/V1)√
P
Radiated RF
IEC 61000-4-3
3 V/m
80 MHz to 2.5 GHz E1 = 3V/m
D=(3.5/E1)√
P80 to 800 MHz
D=(7/E1)√
P800 MHz to 2.5 GHz
Where P is the maximum power rating in watts
and D is the recommended separation
distance in meters.
Fieldstrengthsfromxedtransmitters,as
determined by an electromagnetic site survey,
should be less than the compliance levels (V1
and E1).
Interference may occur in the vicinity of
equipment containing a transmitter.
For transmitters rated at a maximum output power not listed above, the recommended separation distance D in meters
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reectionfromstructures,objects,andpeople.
RecommendedSeparationDistancesBetweenPortableandMobileRFCommunicationsEquipmentandthis
device.ThisdeviceandsystemareNOTLife-Supporting
This device is intended for use in the electromagnetic environment in which radiated disturbances are controlled. The
customer or user of this device can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF Communications Equipment and the device as recommended below, according to the
maximum output power of the communications equipment.
MaximumOutput
Power(Watts)
RecommendedSeparationDistancesforthedevice(meters)
150 kHz to 80 MHz
D=(1.1667)√
P
80 to 800MHz
D=(1.1667)√
P
800 MHz to 2.5 GHz
D=(2.3333)√
P
0.01 0.11667 0.11667 0.23333
0.1 0.36894 0.36894 0.73785
1 1.1667 1.1667 2.3333
10 3.6894 3.6894 7.3785
100 11.667 11.667 23.333
For transmitters rated at a maximum output power not listed above, the recommended separation distance D in meters
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reectionfromstructures,objects,andpeople.

EN - 16
ADVANCED MENU CONTROLS
Withthedeviceon,pressthe“Next”or“Previous”buttonsonthekeypadtoscrollthroughtheitemsonthedisplay.
Name Symbol Function
PREVIOUS ITEM kPressing this button displays the previous menu option.
NEXT ITEM jPressing this button displays the next menu option.
SETTING CHANGE h�
iThese buttons allow you to adjust the setting that is shown on the display.
Please note that the values displayed are examples only.
Patient Menu Layout
The following charts show by Mode each Display you will scroll through using the Next or Previous buttons on the keypad.
Pressing the Down key at the Enable Menu Display will allow you to enter this submenu - then use Next or Previous
buttonstoscrollthroughit;presstheUpbuttontoreturntomainmenu.OncethenalDisplayisreached,pressingthe
NextbuttonwillreturnyoutotherstDisplay.
NOTE-If the unlocked symbol is shown, you are able to adjust this setting. If the locked symbol is shown, this setting can
only be adjusted by your provider.
Auto-OFF 
Enabled
Auto-ON
Enabled
P:10.0 CPAP
Heat:5
SetPressure
10.0cmH20
DelayPressure
5.0cmH20
ComplianceMeter
123456.7hours
SerialNumber
ID123456
Hourmeter
123456.7hours
FirmwareVersion
V0.1321/08/2009
LCDContrastAdj
50%
DelayTime 
10minutes
ExitMenu
Press
EnableMenu
Press
SmartCode1-Day
1FF-FFFF-FWJ
AdherenceScore
83%(25/30)
LowBacklight
Enabled
CPAPMode
NOTE: There are 5 levels of SmartCode data. Use UP 
or DOWN key to change between levels.

EN - 17
Blower Off Menus
Compliance information can be viewed without turning the CPAP on. With the blower OFF (display shows OFF), press the
left or right arrow keys on the keypad to scroll through the information.
DisplayExample Description
OFF Blower OFF, the CPAP unit is plugged in to AC or DC power with the blower OFF.
SerialNumber
HD000005
Shows the serial number of the device.
AdherenceScore
83%(25/30)
Shows the maximum adherence achieved for any period of thirty consecutive days of
use within a ninety-day time frame. The score represents the percentage of days,
within thirty consecutive days, where usage met or exceeded the ‘Usage Threshold.’
SmartCode 1-Day
1FF-FFFF-FWJ
SmartCode Usage
Z7G-7QFM-NWK
SmartCodedataisusedfortherapymanagementreporting;therapyinformationis
encoded in a series of letters and numbers, and includes a special character for error
checking to ensure accuracy. Use the UP arrow or DOWN arrow keys to change the
SmartCode reporting period.
SmartCode Data and Adherence Score Information
Your Healthcare provider may contact you to retrieve SmartCode data and Adherence Score information. To display the
SmartCode data, press the LEFT arrow key once. Use the UP arrow or DOWN arrow keys to change the SmartCode
reporting period. Press the LEFT arrow key again to display the Adherence Score.
Definitions
Notallofthefeaturesinthetablebelowareavailableinallmodels;someareoptionalandsomedependonwhatyour
physician and/or home care provider has selected. The table shows the items you may see, and describes the feature
associated with each item. Also, some features are only available in certain modes or with the DeVilbiss SmartLink
Therapy Management Module – these are noted in the ‘Mode’ column below. If you do not see some of these options, your
modelorcongurationdoesnotsupportthem.
Please note that the values displayed are examples only.
DisplayExample Description
OFF Blower OFF, the CPAP unit is plugged in to AC or DC power with the blower OFF.
P:5.0 Auto
Heat:Off
This is the default screen when the device is turned on. The actual mask pressure
and heater setting are shown. The displayed pressure may vary slightly while
breathing. If the heater system is not connected, the heat setting will be blank.
SetPressure
10.0cmH2O
This is a prescription setting which controls the operating pressure.
DelayTime 
45minutes
Selectable delay time setting. Your provider has set the delay time.
DelayPressure
5.0cmH2O
This is a prescription setting which controls the operating pressure during the delay
time.
EnableMenu
Press
Pressing the down key enters the Enable menu. Refer to next section for Enable
Menu details.

EN - 18
DisplayExample Description
LCDContrastAdj
50%
This setting changes the contrast for the LCD display. This only needs to be adjusted
ifyounditdifculttoseethedisplayfromyourviewingangle.
ComplianceMeter
123456.7hours
The total number of hours (in 1/10 hour increments) that the device has been
providing therapy.
Hourmeter
HD123456
The total number of hours (in 1/10 hour increments) that the device has been in
operation.
FirmwareVersion
V0.1921/08/2009 Showsversionofinstalledrmware.
SerialNumber
HD123456 Shows the serial number of the device.
AdherenceScore
83%(25/30)
Shows the maximum adherence achieved for any period of thirty consecutive days of
use within a ninety-day time frame. The score represents the percentage of days,
within thirty consecutive days, where usage met or exceeded the ‘Usage Threshold.’
SmartCode
1FF-FFFF-FWJ
SmartCode Usage
Z7G-7QFM-NWK
SmartCodeisusedfortherapymanagementreporting;therapyinformationis
encoded in a series of letters and numbers, and includes a special character for error
checking to ensure accuracy. Use the UP arrow or DOWN arrow keys to change the
SmartCode reporting period.
NOTE- If the unlocked symbol is shown, you are able to adjust this setting. If the locked symbol is
shown, this setting can only be adjusted by your provider.

ES - 19
ÍNDICE
Definiciones de símbolos .................................................................................................................................... ES - 19
Precauciones importantes................................................................................................................................... ES - 20
Introducción......................................................................................................................................................... ES - 20
Uso al que se destina................................................................................................................................ ES - 20
Indicaciones de uso................................................................................................................................... ES - 21
Contraindicaciones.................................................................................................................................... ES - 21
Componentes principales.................................................................................................................................... ES - 21
Dispositivo IntelliPAP................................................................................................................................. ES - 21
Teclado ...................................................................................................................................................... ES - 21
Soporte del humidificador.......................................................................................................................... ES - 21
Cámara de agua........................................................................................................................................ ES - 21
Sistema de gestión de terapias................................................................................................................. ES - 21
Montaje del sistema ............................................................................................................................................ ES - 21
Sin humidificador con calentador .............................................................................................................. ES - 21
Con humidificador con calentador............................................................................................................. ES - 21
Teclado y pantalla................................................................................................................................................ ES - 22
Funcionamiento................................................................................................................................................... ES - 22
Inicio .......................................................................................................................................................... ES - 22
Uso de la función de retardo de comodidad ............................................................................................. ES - 22
Control de la humedad.............................................................................................................................. ES - 23
Apagar el dispositivo ................................................................................................................................. ES - 23
Lista del menú Activar ............................................................................................................................... ES - 23
Información sobre puntuación de adherencia y SmartCode®................................................................... ES - 24
Mensajes del paciente......................................................................................................................................... ES - 24
Recordatorios ............................................................................................................................................ ES - 24
Notificaciones ............................................................................................................................................ ES - 24
Información de IntelliPAP en caso de viaje......................................................................................................... ES - 25
Funcionamiento de IntelliPAP con CC ................................................................................................................ ES - 25
Alimentación de batería............................................................................................................................. ES - 25
Oxígeno suplementario ....................................................................................................................................... ES - 25
Accesorios/Piezas de repuesto........................................................................................................................... ES - 26
Mantenimiento..................................................................................................................................................... ES - 26
Limpieza .............................................................................................................................................................. ES - 27
Solución de problemas........................................................................................................................................ ES - 28
Especificaciones.................................................................................................................................................. ES - 30
Declaración del fabricante y guía de uso de DeVilbiss....................................................................................... ES - 31
Controles del menú de propiedades avanzadas................................................................................................. ES - 33
DEFINICIONES DE SÍMBOLOS
Protección eléctrica de clase II: doble
aislamiento Equipo tipo BF – pieza aplicada
Entrada/Salida del puerto de datos Pausa: enciende o apaga el ventilador
Elemento siguiente de la pantalla LCD Aumenta el valor que se muestra en la pantalla LCD
Elemento anterior de la pantalla LCD Disminuye el valor que se muestra en la pantalla LCD
Atención: Consultar los documentos
adjuntos Calor adjuntos
Entrada de CC: 12 VCC, la clavija
entral es positiva 100-240 Voltios de entrada CA 50/60 Hz
Asegurad Desaseg
IPX1 A prueba de goteo, vertical Delay – inicia el ciclo de retardo en el modo de presión positiva
continua en las vías respiratorias (CPAP), si se prescribe
Este dispositivo contiene equipo eléctrico y / o electrónico que debe ser reciclado de acuerdo a la Este
dispositivo contiene equipo eléctrico y / o electrónico que debe ser reciclado de acuerdo a la Directiva EC
2002/96/EC – Equipo Eléctrico y Electrónico de Desecho (WEEE)

ES - 20
PRECAUCIONES IMPORTANTES
LEA TODAS LAS INSTRUCCIONES ANTES DE UTILIZAR ESTE
DISPOSITIVO.
GUARDE ESTAS INSTRUCCIONES
PELIGRO
• Peligrodedescargaseléctricas – No utilizar durante el baño.
• Peligrodedescargaseléctricas – No sumergir este dispositivo en agua ni en ningún otro líquido.
• Peligrodedescargaseléctricas – No intentar abrir ni retirar la carcasa. No contiene componentes que el usuario
pueda reparar o sustituir. Si es necesario reparar el dispositivo, devuelva el producto a su proveedor de servicios de
atención sanitaria domiciliaria. Si abre o altera el producto, la garantía quedará anulada.
ADVERTENCIA
• l dispositivo IntelliPAP de DeVilbiss sólo se debe utilizar con mascarillas recomendadas por DeVilbiss, por el médico
o por el terapeuta respiratorio.
• Para evitar la reinhalación del aire espirado, no utilice la mascarilla de CPAP a menos que el dispositivo esté
encendido y suministrando aire. No bloquee nunca la ventilación de mascarilla. Cuando el dispositivo está
encendido y suministrando aire, el aire espirado se expulsa por el sistema de ventilación de la mascarilla. Sin
embargo, si la unidad de CPAP no está funcionando, es posible reinhalar el aire espirado. La reinhalación del aire
espiradodurantemásdeunosminutosbajodeterminadascircunstanciaspuedeprovocarasxia.Estaadvertencia
se aplica a la mayoría de dispositivos de CPAP.
• La unidad IntelliPAP de DeVilbiss no es un equipo de soporte vital y puede dejar de funcionar si se producen
determinados errores en el dispositivo o si falla el suministro de corriente eléctrica. Está destinado a pacientes con
respiración espontánea de peso superior a 30 kg (66 lbs).
• Para evitar descargas eléctricas, desenchufe siempre el cable de la toma de corriente de la pared antes de limpiar
el dispositivo.
• Utilice sólo accesorios recomendados por DeVilbiss.
• Cuandollenelacámaradeagua,retírelasiempredelsoportedelhumidicador.
• Si se ha derramado agua en el soporte del dispositivo o éste se ha sumergido en agua, desenchufe el cable de la
toma de corriente inmediatamente. Deje que el dispositivo se seque completamente antes de volver a utilizarlo.
• Nobloqueenuncalosoriciosdeairedelacámaranidelsoporte.Noinserteningúnobjetoenningúnoricioni
tubo.
• Paraunfuncionamientoadecuado,coloqueelsistemaenunasupercienivelada,sólidayplana.
• Elusodelhumidicadoropcionalestádestinadoaunúnicopaciente.
• Si coloca el sistema en el suelo, no lo haga donde pueda pisarlo al levantarse de la cama.
PRECAUCIÓN
• El conector circular del puerto de datos que se encuentra en la parte posterior del dispositivo IntelliPAP permite
conectar los accesorios. El conector sólo se deberá utilizar con accesorios cuyo uso haya sido aprobado por
DeVilbiss. No intente adjuntar ningún otro tipo de dispositivo a este conector, ya que podría dañar la unidad o el
dispositivo suplementario.
• No enjuague nunca el dispositivo ni lo sumerja en agua. Nunca permita que entre ni haya líquido cerca de los
puertos,delosinterruptoresodelltrodeaire,yaquepodríanproducirsedañoseneldispositivo.Siestoocurriera,
desenchufe el cable de la toma de corriente inmediatamente. Deje que el dispositivo se seque completamente antes
de volver a utilizarlo.
• No coloque el dispositivo IntelliPAP donde pueda sufrir una caída o donde alguien pueda tropezar con el cable de
corriente.
• SerecomiendausarsóloelsistemahumidicadorconcalentadorDeVilbissDV5coneldispositivoIntelliPAP.Es
posiblequeotrossistemasdehumidicaciónimpidanqueeldispositivodetectelosronquidosyproduzcanunos
niveles de presión inadecuados.
• Antes de transportar el dispositivo, vacíe y seque la cámara de agua.
INTRODUCCIÓN
Uso al que se destina/Indicaciones de uso
El modelo DeVilbiss IntelliPAP serie DV51 Standard está destinado al uso para el tratamiento de la apnea obstructiva del
sueño (AOS) en pacientes que respiren de manera espontánea con un peso de 30 kg (66 lbs) o más mediante medios de
aplicación de presión positiva de aire. El dispositivo es para uso en el hogar y en entornos clínicos.