ResMed-VPAP-Combined Service-Manual PDF
ResMed-VPAP-Combined Service-Manual PDF
ResMed-VPAP-Combined Service-Manual PDF
VPAP Auto 25
VPAP ST
VPAP S
VPAP IV ST
VPAP IV
S8 Auto 25
English
268299/4 2012-03
2 Introduction ......................................................................... 5
Intended users of this manual 5
Nasal CPAP 5
Features of the VPAP range 5
Contents 3
1 How to use this manual
Each of the sections in this manual have been written with a specific purpose in mind. Use this
guide to help you find the material which is relevant to your task at the moment.
2 Introduction – Gives a brief overview of the current VPAP™ range.
3 General inspection and servicing – Gives the procedures to help you examine a flow
generator which has been brought into a service centre. The general inspection procedures
should be performed before any other work is done on the flow generator.
4 Operator safety and static precautions – Provides safety advice and lists procedures to be
followed whenever PCBs are removed from the flow generator. These procedures minimize the
chance of ICs being damaged by static electricity.
5 Replacing major subassemblies – Highlights points to note when replacing subassemblies,
reassembling the flow generator and indications of when recalibration is necessary.
6 Replacement parts – Shows labelled pictures and part numbers of all the spare parts and
subassemblies available from ResMed.
7 Calibration procedures – Procedures to follow after a fault has been isolated to a PCB, the
blower or the flow meter, and the part has been replaced. Follow these procedures to calibrate
the unit. Once calibrated, restore the owner’s individual settings.
8 Troubleshooting guide – Gives you a way to quickly locate the problem and fix it if you know
the symptoms of a faulty machine.
9 System specifications – Lists electrical and mechanical specifications of the flow generator
and air tubing.
10 Recommended maintenance schedule – Provides a brief description of the maintenance
which the owner of the flow generator should carry out.
Some countries require all medical equipment to have a periodic service to confirm that the
equipment is in good working order. Section 3, “General inspection and servicing” may be
used in this situation.
Appendix A: Service Request Form - Fill out this form if you need to return a device to ResMed
for servicing.
Appendix B: Operational diagram - Provides a pictorial representation of the flow generator
function.
Note: Schematics of all PCBs in these flow generators are available to authorised service
centres. To order, please contact your local ResMed office.
This manual contains special terms and icons that appear in the margins to draw your attention to
specific and important information.
• Warning alerts you to possible injury.
• Caution explains special measures for the safe and effective servicing of the device.
• Note is an informative or helpful note.
• VPAP ST • S8 Auto 25
• VPAP IV • VPAP IV ST
It is written for ResMed distributors, and gives instructions for replacing subassemblies and for
recalibration as appropriate. Work at the component level will normally be carried out by ResMed.
Nasal CPAP
Nasal Positive Airway Pressure systems are used to treat obstructive sleep apnea (OSA), a disorder
that causes a physical obstruction in a person’s airway while sleeping. The principle of treatment is
that filtered air is delivered by a flow generator through flexible tubing to a nasal mask worn by the
patient while sleeping. The flow generator maintains a positive pressure in the patient’s airway
which acts as a pneumatic splint, preventing the airway from collapsing during sleep.
CPAP
VAuto
S (Spontaneous)
S/T (Spontaneous/Timed)
T (Timed)
Note: Schematics of all PCBs in this flow generator are available to authorised service centres.
To order, please contact your local ResMed office.
2 Introduction 5
3 General inspection and servicing
Instructions for general inspection procedures
Carry out the procedures on the following pages to confirm that the VPAP is in good electrical and
mechanical condition. These tests will highlight any major mechanical or electrical problem with the
unit.
Equipment required
• ResMed Service Software 1.20, available from the Technical Services website.
Note: Ensure you check the Technical Services website to confirm the latest version of service
software available for use with this product.
Function keys
LCD screen
Up key
Down key
Start/Stop key
Warning When using a cleaning agent with a high alcohol content refer to the appropriate Material
Safety Data Sheet to ensure safe handling of the cleaning agent.
!
Remove any stains from the cases. When removing any stains from the flow generator or mask
system use soap or detergent-based cleaning solutions. Remove excess and wipe dry after use.
Do not use thinners, trichlorethylene, bleach or other solvents. Do not apply oil to any component
of the flow generator.
4 Turn on the flow generator and allow it to complete the self test.
5 Connect the flow generator to the PC via the USB cable.
XPlorer
bar
Refresh
button
7 Press the Refresh button (as indicated above) to enable the service software to recognise the
flow generator.
8 The flow generator details will then be displayed at the bottom of the screen beside the Refresh
button. The calibration and tests in the Xplorer bar at the left of the screen will also change to
indicate the procedures specific for that product.
9 Select Flow Generator Settings... in the XPlorer bar, or click on the Flow Generator Setting
Dialog icon at the top of the screen.
10 Note: It will take a few seconds for the flow generator settings to be displayed.
11 The flow generator settings will be displayed as shown below:
Create a new
Service Setting
Record icon
15 At this point, you can select the name of the service agent handling the device and enter the
Service Record (SR) and Repair numbers, so that this information will be included with the flow
generator settings details.
Note: To enter new service agent details, click on the image in the "Select service agent"
window. A cursor will then appear in the "Service Agent" field, and the name can be
entered.
Once the service agent details are entered, any service agent names entered for that
device will be available for selection in the drop down menu.
If an existing session was selected, the "Select service agent" window will already be
populated.
Warning If the clinical settings cannot be recorded, select the appropriate product code for the
product. In the XPlorer bar, click on "Read default settings", then click on "Reload to flow
! generator". Notify the patient, so they can have their settings reloaded.
16 Click on the Select button once the details have been entered.
17 The software will then return to the settings screen.
18 Turn off the flow generator and disconnect the serial adapter.
19 Refit the data card module.
Warning The VPAP range uses an isolated power supply, however, it is recommended that isolation
transformers are also used for added safety while working with the cases opened up and
! power switched on.
Remove the top case and chassis lid by following the instructions given in Section 5 Replacing
major subassemblies. Inspect the flow generator for the following, recording any irregularities:
• The main PCB is seated correctly
• The blower assembly is seated correctly
• The flow meter is seated correctly
• The power supply PCB is seated correctly
Inspect the unit for the following, recording any irregularities:
• all mechanical components are seated correctly
• all electrical components are mounted correctly and secured in position
• there are no loose terminals, loose wires or incomplete insulation on electrical components or
connections
• there are no loose pieces of wire or other objects trapped in the PCB
Use an antistatic cloth or brush to remove dust or dirt from components and from the insides of
the flow generator case.
Repair or replace any missing or damaged external components. Rectify any problems either
identified by the user or noted during servicing. Should any major components such as the blower
assembly, the flow meter or the main PCB require replacement the flow generator should be
recalibrated and tested after the assembly has been replaced. Follow the procedures in Section 7
Calibration procedures to calibrate the unit, then repeat tests 6-17 in Section 3 General
inspection and servicing.
Reassemble the flow generator.
Caution Printed circuit boards can be damaged by static electricity. Please read the instructions in
Section 4 Operator safety and static precautions before attempting to replace any
! PCBs.
Thread cutting screws are used throughout the flow generator. When replacing a thread
cutting screw, turn the screw anti-clockwise until it fits into the previously cut thread.
Otherwise the original thread may be stripped out.
Caution Only use genuine ResMed spare parts, because the filter affects the flow characteristics
of the flow generator, which in turn affects the pressure supplied to the patient.
!
7 H4i test
The VPAP range is designed to integrate with the H4i heated humidifier to form a single flow
generator with humidification unit. The flow generator automatically detects the H4i docking
station when it is connected to the flow generator.
4 Switch on the flow generator and observe the LCD screen. After a Welcome message is
displayed, the LCD should display the warm-up feature prompt. If the Mask fit screen is
displayed, press the Right key to exit.
Note: It may be difficult to determine if the humidifier light is on in a brightly lit room.
7 Press the Right key again to stop the warm-up feature.
8 Switch off the flow generator and remove the H4i docking station.
Caution Make sure the flow generator has been warmed up for at least 15 minutes before
proceeding with the remaining tests.
!
1 With the unit still switched off, remove the data card module and refit the ResScan USB
adaptor, with USB cable attached.
2 Turn on the unit and allow it to complete the self test.
3 Return to the service software and press the Record button .
4 The following screen will then appear, indicating the existing service records for the flow
generator.
5 The most recently created record (the flow generator settings recorded earlier) will be
highlighted.
6 Click on the Select button to continue recording the service results to the same record.
7 The "Select service agent screen", as shown on page 9, will appear once again.
8 Select the name of the service agent and enter the SR number.
9 All calibration and tests, including tests completed without service software are then listed in
the Xplorer bar.
10 Select Pressure calibration test in the XPlorer bar, or click on the Perform the pressure
calibration test icon .
Note: At the top of the screen at the beginning of each procedure is an alert reminding you to
reload the clinical settings to the unit after completing the necessary test and calibration
procedure. Click the OK button once you have read the alert.
12 Blower test
1 Select Blower test in the XPlorer bar, or click on the Perform the blower test icon .
2 Set up the test equipment as instructed by the test software.
3 Select Next and follow the steps as instructed.
If the flow generator fails this test, repeat the pressure calibration, ensuring the test set-up is
correct. If the unit continues to fail, refer to Section 7 Troubleshooting guide.
13 Keypad test
1 Select Keypad test in the Xplorer bar, or click on te Perform the keypad test icon .
2 The test set-up remains the same as the blower test.
3 Select Next and follow the steps as instructed.
If the flow generator fails this test, refer to Section 8 Troubleshooting guide.
14 LCD test
1 Select LCD test in the XPlorer bar, or click on the Perform the LCD test icon .
2 Follow the steps as instructed.
If the flow generator fails this test, refer to Section 7 Troubleshooting guide.
1 Click on the name of each manual check. A screen such as that shown below will be displayed:
For each manual check, indicate whether the unit passed or failed.
17 Set clock
Note: Ensure that the PC used to service the flow generator is set to the correct date and time
prior to pressing the Set time and date icon.
1 Select Set time and date... in the XPlorer bar, or click on the Read and adjust flow generator
clock icon .
2 The following window will appear:
5 All recorded sessions for the unit will be displayed. Ensure the most recent session (in which
the clinical settings and results were recorded) is highlighted, then click the Select button .
6 The screen will then be repopulated with the original settings. Select Reload to flow generator
in the Xplorer bar to load the settings back into the unit.
7 Once complete, exit the settings screen.
8 Once again, press the Record button and ensure the most recent session (in which the clinical
settings and results were recorded) is highlighted, then click on the Select button .
9 Click on Reload settings at the bottom of the Xplorer bar.
11 Click on the Select button to indicate that the clinical settings were successfully reloaded into
the flow generator.
12 Press the Record button if you did not need to fill out the product problem report or print out the
test results.
Caution When the main PCB, flow meter or motor is replaced, the flow generator must be
recalibrated and tested. Follow the procedures in Section 7 Calibration procedures to
! calibrate the unit, then repeat tests 6-17 in Section 3 General inspection and servicing.
Printed circuit boards can be damaged by static electricity. Please read the instructions in
Section 4 Operator safety and static precautions before attempting to replace any
PCBs.
Thread cutting screws are used throughout the flow generator. When replacing a thread
cutting screw, turn the screw anti-clockwise until it fits into the previously cut thread,
otherwise the original thread may be stripped out.
Top case
Handle
Interface panel
Power outlet
Air outlet
Bottom case
Rear view
Data card
module
Filter
DC input
AC input
2 Grasp both the top and bottom case at the rear of the unit, and prise them apart. Alternatively,
lift upwards on the handle to remove the top case.
3 With the top case removed the main PCB and LCD are now visible.
LCD backlight
cable
Flow sensor
cable harness LCD
Main PCB
Caution When the main PCB, flow meter or motor is replaced, the flow generator must be
recalibrated and tested. Follow the procedures in Section 7 Calibration procedures to
! calibrate the unit, then repeat tests 6-17 in Section 3 General inspection and servicing.
1 Disconnect the flow sensor cable harness from the main PCB.
3 Pinch the sides of the motor connector to disconnect the tabs (circled) from the pcb. Continue
to pull on the cable to disconnect the pins from the PCB.
4 Lay the sensor tube in the route shown below, ensuring the pressure port fitting sits in the
chassis nest.
5 Insert the cable harness between the chassis cable pins and lay it in the route shown below,
ensuring the harness sits under the cable retention ribs and lays in the nest indicated.
Pressure port
in chassis nest
Read default
settings
6 The screen will then be populated with the units default settings.
7 Click on Reload to flow generator to load them into the unit.
8 Exit the Settings screen.
9 Once again, press the Record button and ensure the most recent session (in which the clinical
settings and results were recorded) is highlighted, then click on the Select button .
10 Click on Reload settings at the bottom of the Xplorer bar.
11 The following window will be displayed:
Flexible cable
Locking device
3 Turn the main PCB upside down, and disengage the mounting snaps (circled) from the main
PCB.
5 Engage the middle mounting snaps, then the front mounting snaps to the main PCB.
6 Relocate the flexible cable in the locking device.
7 Reconnect the LCD backlight connector.
Caution When the main PCB, flow meter or motor is replaced, the flow generator must be
recalibrated and tested. Follow the procedures in Section 7 Calibration procedures to
! calibrate the unit, then repeat tests 6-17 in Section 3 General inspection and servicing.
Note: Whenever the chassis lid is removed, the lid needs to be replaced to ensure an effective
seal with the chassis.
1 With the main PCB removed the blower module assembly is visible.
2 Remove the three screws circled below:
3 Remove the sensor tube and release the cable harness from the cable retention ribs.
4 Pull upwards on the lid to remove it from the three locating posts.
Motor wiring
harness
Motor
Outlet seal
Flow sensor
3 Lift the silicone sleeve up off the two locating posts (circled), next to the motor cable.
5 With the sleeve removed the impeller on the base is now visible.
6 Take the silicone sleeve and begin to refit it over the air outlet.
7 Ensure the sleeve sits in the channel surrounding the air outlet.
8 Refit the holes in the sleeve over the locating posts, next to the motor cable.
9 Clip the motor cable into place.
2 Insert the new motor assembly into the bottom case, while guiding the outlet seal into the
retaining slot.
Outlet seal
positioning
feature
Wiring harness
(with heat shrink) Motor connector
in channel in retaining slot
Note: Ensure the wiring harness has been fully inserted in the channel.
5 Install the new chassis lid.
Note: Whenever the chassis lid is removed, the lid needs to be replaced to ensure an effective
seal with the chassis.
6 Install the screws removed earlier in the order shown below.
7 Gently pull the outlet seal tab to ensure a proper seal is formed around the outlet.
Pressure port
in chassis nest
3 With the blower module assembly removed the power supply PCB can be replaced.
Note: At this point the bottom case acoustic foam can also be replaced.
4 Lift the power supply PCB upwards to remove it from the bottom case.
5 Insert the new power supply PCB into the bottom case, ensuring it is correctly located in the
mounting slots.
6 Carefully refit the blower module assembly, ensuring the power supply pins are not bent or
damaged.
8 Ensure the blower module assembly is sitting correctly in the bottom case, with the base of the
outlet flush to the bottom case, as shown below:
2 3
Caution When the main PCB, flow meter or motor is replaced, the flow generator must be recalibrated and
tested. Follow the procedures in Section 7 Calibration procedures to calibrate the unit, then
! repeat tests 6-17 in Section 3 General inspection and servicing.
With the blower module assembly removed from the bottom case, the flow sensor can be
replaced.
1 Remove the chassis lid. The flow sensor is now visible.
Flow
sensor
2 Push downwards on the flow sensor seal to disconnect it from the chassis.
3 Gently pull down on the sensor and the flow sensor cable harness in order to disengage the
grommet from the chassis. Ensure you do not damage the cable harness or connector.
Cable harness
6 Fit the seal to the new flow meter, ensuring the arrow on the flow meter is pointing towards the
seal.
7 Feed the cable harness through the underside of the chassis, ensuring you do not damage the
cable harness or connector.
Grommet
Flow meter
Lock tab
Lock tabs
2 Remove the keypad from the interface panel, taking care not to touch the pills on the back of the
keypad. At this point both the interface panel and keypad can be replaced.
3 With the interface panel removed the handle can be replaced. Lift the handle and slide it
forwards to disengage it from the retaining slots.
6 Take the interface panel and place it on the top case. Press down on the interface panel to
engage the lock tabs which anchor it to the top case.
7 Turn the top case upside down and confirm that all three lock tabs are engaged.
3 Turn the unit right side up, and refit the filter and filter cover, with the blue side of the filter
material facing out from the flow generator.
Outside cases
Also available
Handle R330-718
Type PT, Self tapping screw, 3 x 25 mm, Torx pan head Z2021
Interface panel
VPAP Auto 25 R261-7126
VPAP S R261-7165
VPAP ST R261-7148
S8 Auto 25 (GER, FRA, EUR 1 & 2, UK) R261-7160
VPAP IV (GER) R261-7162
VPAP IV (EUR 1 & 2, UK, FRA, AP) R261-7149
VPAP IV (ANZ) R261-7155
VPAP IV ST (GER) R261-7163
VPAP IV ST (EUR 1 & 2, UK, FRA, AP) R261-7150
VPAP IV ST (ANZ) R261-7164
Internal components
Main PCBs
VPAP Auto 25 19474
VPAP IV (ROW) 19487
VPAP IV ST (ROW) 19488
VPAP ST (US) 19489
VPAP S (US) 19490
S8 Auto 25 (ROW) 19492
Battery E9025
LCD 19327
Equipment required
• ResMed Service Software 1.20, available from the Technical Services website.
Note: Ensure you check the Technical Services website to confirm the latest version of service
software available for use with this product.
• ResScan USB adaptor and cable (ResMed part #22203)
• Oxygen side port connector
• Straight adaptor
• Calibration cap
• Air tubing connector
Note: The above four items are contained in the Service accessories kit (#19919) - this kit
includes S9 adapter and USB cable, oxygen sideport connector, straight adaptor,
calibration cap and air tubing connector.
Cautions The flow generator clinical settings must be recorded before any calibration procedure is
! performed. Refer to the instructions provided in Section 3 General inspection and
servicing. If the clinical settings cannot be recorded, select the appropriate product code
for the product. In the XPlorer bar, click on "Read default settings", then click on "Reload to
flow generator". Notify the patient, so they can have their settings reloaded.
1 Pressure calibration
Warm up the flow generator for at least 15 minutes before commencing the calibration
procedures.
1 With the unit still switched off, remove the data card module and refit the ResScan USB
adaptor, with USB cable attached.
2 Turn on the unit and allow it to complete the self test.
3 Return to the service software and press the Record button .
4 The following screen will then appear, indicating the existing service records for the flow
generator.
7 Calibration procedures 45
5 The most recently created record (the flow generator settings recorded earlier) will be
highlighted.
6 Click on the Select button to continue recording the service results to the same record.
7 The "Select service agent screen", as shown on page 10, will appear once again.
8 Select the name of the service agent and enter the SR number.
9 All calibration and tests, including tests completed without service software are then listed in
the Xplorer bar.
10 Select Pressure calibration in the XPlorer bar, or click on the Perform the pressure calibration
icon .
Note: At the top of the screen at the beginning of each procedure is an alert reminding you to
reload the clinical settings to the unit after completing the necessary test and calibration
procedure. Click the OK button once you have read the alert.
2 Flow calibration
Caution The pressure calibration must be performed before the flow calibration.
!
1 Select Flow calibration in the XPlorer bar, or click on the Perform the flow calibration icon .
2 Set up the test equipment as instructed by the test software.
3 Select Next and follow the steps as instructed until the calibration is complete.
Caution The pressure calibration and flow calibration must be performed before the motor noise
calibration.
!
1 Select Motor noise calibration in the XPlorer bar, or click on the Perform the motor noise
calibration icon .
2 Set up the test equipment as instructed by the test software.
3 Select Next and follow the steps as instructed until the calibration is complete.
Once the calibrations are complete, repeat tests 6-17 from Section 3 General inspection and
servicing.
If the unit continually fails the calibration, check the following:
• the test set-ups are correct
• the calibration cap is securely attached and there are no leaks in the air delivery system
• the unit has no excess noise or vibration, which may be caused by a problem with the blower.
If the unit continues to fail, send the flow generator with service request form (found on page 57 of
this manual) to ResMed for further servicing.
If any other components are replaced, repeat the relevant tests in Section 3 General
inspection and servicing
Note: The performance tests in the service software are a valuable tool in determining the
possible cause of flow generator problems.
Problem/Cause Action
No display
• Flexible cable from LCD not inserted properly into • Check flexible cable is connected properly
connector
• Flexible cable from LCD not inserted properly into • Check flexible cable is connected properly
connector
• Pills on the back of the keypad or LCD have been • Replace keypad or LCD
damaged
• Gold contacts on main PCB dirty • Clean contacts. Refer to “4 Internal examination (if
necessary)” on page 10.
• Ramp time is in use • Wait for air pressure to build up or change ramp time
• Air tubing not connected properly • Check and refit tubing as required
• Blown fuse in power supply • Replace and investigate cause of the blown fuse
8 Troubleshooting guide 47
Problem/Cause Action
Flow generator operating intermittently
• Leak alert not enabled in clinical menu • Confirm if patient required leak alert enabled.
Note: When leak alert is on, SmartStart/Stop is automatically
set to off. SmartStart/Stop cannot be used with leak alert
because, if a high leak occurs, SmartStop may stop
treatment before the leak alert alarm is activated.
Unit cannot maintain correct date and time ("used sessions.total days" ratio display may also be invalid
Flat Real time clock battery 1 Download compliance data and record clinical settings.
2 Replace battery
3 Reset the time and date
4 Erase compliance data from the unit
The following message is displayed on the LCD: "CHECK TUBE!!! KEY IF DONE"
Air tubing is loose or blocked Check tubing is connected to flow generator and mask.
Confirm nothing is blocking air tubing.
The following message is displayed on the LCD: "SYSTEM ERR 101F Call service!"
The following message is displayed on the LCD: "SYSTEM ERR 101A Call service!"
The following message is displayed on the LCD: "SYSTEM ERR 101B Call service!"
The following message is displayed on the LCD: "SYSTEM ERR 1014 Call service!"
The following message is displayed on the LCD: "SYSTEM ERR 1015 Call service!"
• Sensor tubing damaged or crushed • Confirm sensor tubing is installed correctly and not
restricted in any way
The following message is displayed on the LCD: "SYSTEM ERR 1018 Call service!"
The following message is displayed on the LCD: "SYSTEM ERR 1019 Call service!"
The following message is displayed on the LCD: "SYSTEM ERR 107A Call service!"
The following message is displayed on the LCD: "SYSTEM ERR 1068 Call service!"
• Flow generator has been covered with a blanket 1 Inform user not to cover unit
2 Allow flow generator to cool down
3 Power-cycle to remove message
8 Troubleshooting guide 49
9 System specifications
VPAP Auto 25, VPAP ST, VPAP S
Operating pressure range: 3 to 25 cm H2O
Maximum single fault pressure: 40 cm H2O
Pressure measurement tolerance: ± 0.5 cm H2O ± 4% of the measured reading
Flow measurement tolerance: ± 0.1 L/sec or 20% of reading, whichever is greater
VAuto mode: 4 to 25 cm H2O (measured at the mask); Min EPAP: 4 cm H2O; Max IPAP:
25 cm H2O; Pressure support: 0 to 10 cm H2O
S, ST and T mode: IPAP: 4 to 25 H2O (measured at the mask); EPAP: 3 to 25 cm H2O
(measured at the mask)
CPAP mode: 4 to 20 cm H2O (measured at the mask)
DECLARED DUAL-NUMBER NOISE EMISSION VALUES in accordance with ISO 4871:
Sound pressure level: 26 dBA with uncertainty of 2 dBA as measured according to ISO17510-
1:2002
28 dBA with uncertainty of 2 dBA as measured according to ISO17510-
1:2007
Sound power level 36 dBA with uncertainty of 2 dBA as measured according to ISO17510-
1:2007
Dimensions (LxWxH): 4.4" x 6.5" x 5.7" (112 mm x 164 mm x 145mm)
Weight: 2.9 lb. (1.3 kg)
Power supply: Input range 100-240V, 50-60 Hz, 40VA (typical power consumption), <
100VA (maximum power consumption
Housing construction: Flame retardant engineering thermoplastic
Operating temperature: 41° F to 95° F (+5°C to +35°C)
Operating humidity: 10%-95% non-condensing
Storage and transport temperature: -4°F to +140°F (-20°C to +60°C)
Storage and transport humidity: 10%-95% non-condensing
Operating altitude: Sea level to 8500’ (2600 m)
Electromagnetic compatibility: Product complies with all applicable electromagnetic compatibility
requirements (EMC) according to IEC60601-1-2, for residential, commercial
and light industry environments.
Air filter: Two layered, powder-bonded, polyester non-woven fibre
Air tubing: Flexible plastic, 1 x 6’6" (2 m)
Air outlet: The 22 mm conical air outlet complies with EN ISO 5356-1
IEC 60601-1 classification: Class II (double insulated), Type CF
Note: The manufacturer reserves the right to change these specifications without notice.
Pressure Accuracy
Maximum static pressure variation at 10 cm H2O according to ISO 17510-1:2007:
9 System specifications 51
VPAP IV, VPAP IV ST
Operating pressure range: 2 to 25 cm H2O
Maximum single fault pressure: 30 cm H2O
Flow measurement tolerance: ± 0.1 L/sec or 20% of reading, whichever is greater
S, ST and T mode: IPAP: 4 to 25 H2O (measured at the mask); EPAP: 2 to 25 cm H2O
(measured at the mask)
CPAP mode: 4 to 20 cm H2O (measured at the mask)
Flow at set pressures: (measured 4 cm H2O 204 (L/min)
at end of standard 2 m tubing) 8 cm H2O 213 (L/min)
12 cm H2O 202 (L/min)
16 cm H2O 180 (L/min)
20 cm H2O 169 (L/min)
Note: The manufacturer reserves the right to change these specifications without notice.
Pressure Accuracy
Maximum static pressure variation at 10 cm H2O according to ISO 17510-1:2007:
Environmental information
WEEE2002/96/EC is a European Directive that requires the proper disposal of electrical and electronic equipment. This device
should be disposed of separately, not as unsorted municipal waste. To dispose of your device, you should use appropriate
collection, reuse and recycling systems available in your region. The use of these collection, reuse and recycling systems is
designed to reduce pressure on natural resources and prevent hazardous substances from damaging the environment.
If you need information on these disposal systems, please contact your local waste administration. The crossed-bin symbol
invites you to use these disposal systems. If you required information on collection and disposal of your ResMed device
please contact your ResMed office, local distributor or go to www.resmed.com/environment.
9 System specifications 53
S8 Auto 25
Operating pressure range: 4 to 25 cm H2O
Maximum single fault pressure: 40 cm H2O
Pressure measurement tolerance: ± 0.5 cm H2O ± 4% of the measured reading
Flow measurement tolerance: ± 0.1 L/sec or 20% of reading, whichever is greater
V Auto mode: 4 to 25 H2O (measured at the mask); Pressure support: 0 - 10 cm H2O
CPAP mode: 4 to 20 cm H2O (measured at the mask)
DECLARED DUAL-NUMBER NOISE EMISSION VALUES in accordance with ISO 4871:
Sound pressure level: 26 dBA with uncertainty of 2 dBA as measured according to ISO17510-
1:2002
28 dBA with uncertainty of 2 dBA as measured according to ISO17510-
1:2007
Sound power level 36 dBA with uncertainty of 2 dBA as measured according to ISO17510-
1:2007
Dimensions (LxWxH): 112 mm x 164 mm x 145mm
Weight: 1.3 kg
Power supply: Input range 100-240V, 50-60 Hz, 40VA (typical power consumption), <
100VA (maximum power consumption
Housing construction: Flame retardant engineering thermoplastic
Operating temperature: +5°C to +35°C
Operating humidity: 10%-95% non-condensing
Storage and transport temperature: -20°C to +60°C
Storage and transport humidity: 10%-95% non-condensing
Operating altitude: Sea level to 2600 m
Supplemental oxygen: Recommended maximum supplemental oxygen flow: 4 L/min
Electromagnetic compatibility: Product complies with all applicable electromagnetic compatibility
requirements (EMC) according to IEC60601-1-2, for residential, commercial
and light industry environments.
Air filter: Two layered, powder-bonded, polyester non-woven fibre
Air tubing: Flexible plastic, 1 x 2 m
Air outlet: The 22 mm conical air outlet complies with EN ISO 5356-1
IEC 60601-1 classification: Class II (double insulated), Type CF
Notes: The manufacturer reserves the right to change these specifications without notice.
Pressure may be displayed in cm H2O or hPa.
Pressure Accuracy
Maximum static pressure variation at 10 cm H2O according to ISO 17510-1:2007:
Environmental information
WEEE2002/96/EC is a European Directive that requires the proper disposal of electrical and electronic equipment. This device
should be disposed of separately, not as unsorted municipal waste. To dispose of your device, you should use appropriate
collection, reuse and recycling systems available in your region. The use of these collection, reuse and recycling systems is
designed to reduce pressure on natural resources and prevent hazardous substances from damaging the environment.
If you need information on these disposal systems, please contact your local waste administration. The crossed-bin symbol
invites you to use these disposal systems. If you required information on collection and disposal of your ResMed device
please contact your ResMed office, local distributor or go to www.resmed.com/environment.
9 System specifications 55
10 Recommended maintenance schedule
The VPAP devices are intended to provide safe and reliable operation when operated in accordance
with the instructions provided by ResMed. ResMed recommends that these devices be inspected
and serviced by an authorised ResMed Service Centre if there is any sign of wear or concern with
device function. Otherwise, service and inspections of the devices generally should not be
required during the five year design life of the product.
Procedures for filter replacement and regular cleaning are provided in the User Manual. All of these
procedures can be carried out by the owner.
Some countries require all medical equipment to have a periodic service to confirm that the
equipment is in good working order. Section 3 General inspection and servicing may be used in
this situation.
Problem details
Product details
Product code Mask type
Under warranty? Yes No
Product name Pressure settings
Humidifier? Yes No
Serial/Lot number Hourmeter reading
SmartStart? Yes No
Problem description
Effect on user
Date of purchase Or
If the purchase date is unknown, please indicate below the time the product was used before the problem occurred
When did the fault occur? Not being used During use Start up Unknown
Service details
ResMed reference number Distributor reference number (if applicable) Today’s date
Signature
AUF 19019-01/5