Cardinal Health NPWT PRO User manual

NPWT PRO and PRO to GO
PATIENT USER MANUAL

Patient User Manual

Patient User Manual
About Your Cardinal Health™ NPWT PRO / PRO to GO
Your doctor has chosen the Cardinal Health™ NPWT PRO / PRO to GO device to remove uid from your wound by using
carefully controlled suction. It is important, however, for you to carefully watch the wound and the Cardinal Health™ NPWT
PRO family device to make sure that the device is working properly. Below is some important information and questions
that you should ask your Healthcare Professional.
Things you need to know about your Cardinal Health™ NPWT PRO family device
• Do not allow the Cardinal Health™ NPWT PRO family device to get wet. Clamp the tube and disconnect from the
canister if you take a bath or shower.
• Keep the Cardinal Health™ NPWT PRO family device plugged in whenever possible to keep the battery fully charged.
Always take the power cord with you when you leave home.
• Keep the Cardinal Health™ NPWT PRO family device upright to avoid a false canister full alarm.
• Keep the Cardinal Health™ NPWT PRO family device turned on at all times unless there is bleeding from the wound
or instructed by your Healthcare Professional.
• Do not change the settings on the Cardinal Health™ NPWT PRO family device unless you are told to do so by your
Healthcare Professional.
Things to ask your Healthcare Professional
• How to tell if there is a problem with your Cardinal Health™ NPWT PRO family device or dressing.
• What to do if you have a problem or a leak with your dressing.
• What to do if you notice bleeding from the wound.
• What to do if you must take your dressing o.
• What activities you can do while using the Cardinal Health™ NPWT PRO family device.
• Who to call if you need help.
• How to take care of your Cardinal Health™ NPWT PRO family device.

Patient User Manual
CAUTION: This Cardinal Health™ NPWT PRO / PRO to GO (herein after referred to as the Cardinal Health™ NPWT PRO
family of devices) PATIENT User Manual is not a guarantee or warranty. It is intended only as an operational guide.
For additional information and questions, please contact Cardinal Health Customer Service at 1.866.484.6798.
In order for the Cardinal Health™ NPWT PRO family of devices to provide safe, reliable, and proper performance, the
following conditions must be met. Failure to comply with these conditions will void all pertinent warranties.
• There are no user serviceable components in the Cardinal Health™ NPWT PRO family of devices. All assembly,
operation, adjustment, modication, maintenance, and/or repair must be carried out only by qualied personnel
authorized by Cardinal Health.
• The electrical installation of the room in which the device will be used complies with the appropriate national
electrical standards.
• The product must be used in accordance with this manual and all associated labeling and the Instructions for Use.
• Any device that does not function as expected must be returned to Cardinal Health.
Notice to Users: CAUTION: Federal law restricts this device to sale by or on the order of a physician. As with any
prescription medical device, failure to follow product instructions or changing settings and performing therapy applications
without the express direction and/or supervision of a trained clinical caregiver may lead to improper product performance
and the potential for serious or fatal injury.

Patient User Manual
Table of Contents
1. Introduction.................................................................................................................................................................. 4
1.1 Indications.............................................................................................................................................................. 4
1.2 Contraindications ................................................................................................................................................... 4
1.3 Precautions ............................................................................................................................................................ 4
1.4 Additional Precautions ........................................................................................................................................... 4
1.5 Safety Tips.............................................................................................................................................................. 5
2. Introduction to the Cardinal Health™ NPWT PRO Family of Devices............................................................................... 6
2.1 Getting to know the Cardinal Health™ NPWT PRO Family of Devices...................................................................... 6
2.2 Charging the Battery.............................................................................................................................................. 7
3. Operating Instructions................................................................................................................................................... 8
3.1 Power ON/OFF ........................................................................................................................................................ 8
3.2 Power-up Procedure............................................................................................................................................... 8
3.3 Alarm Operation..................................................................................................................................................... 8
4. Care and Cleaning ....................................................................................................................................................... 10
4.1 Disposal of Dressings, Canister and Other Disposables.......................................................................................... 10
4.2 Cleaning the Device.............................................................................................................................................. 10
4.3 AC Power Adapter Inspection ............................................................................................................................... 10
5. Specications.............................................................................................................................................................. 11
5.1 Symbols................................................................................................................................................................ 12
5.2 Electromagnetic Compatibility ............................................................................................................................. 13
6. Replacement Parts ...................................................................................................................................................... 15
7. Questions & Information............................................................................................................................................. 16

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Patient User Manual
1. Introduction
1.1 Indications
The Cardinal Health™ NPWT PRO/PRO to GO systems are an integrated wound management system, indicated for the
application of continual or intermittent negative pressure wound therapy to the wound as the device may promote
wound healing by the removal of uids, including wound exudates, irrigation uids, body uids and infectious
materials. The Cardinal Health™ NPWT PRO/PRO to GO systems are intended for patients with chronic, acute, traumatic,
subacute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), aps and grafts. The
Cardinal Health™ NPWT PRO/PRO to GO systems are intended for use in acute, extended and home care settings.
1.2 Contraindications
The Cardinal Health™ NPWT PRO / PRO to GO is contraindicated for patients with malignancy in the wound,
untreated osteomyelitis, non-enteric and unexplored stulas, or necrotic tissue with eschar present. Do not place
the Cardinal Health™ NPWT foam dressing over exposed blood vessels or organs.
1.3 Precautions
Precautions should be taken for patients with infected wounds, active bleeding, dicult wound hemostasis, or who are
on anticoagulants.When placing the foam dressing in close proximity to blood vessels or organs, take care to ensure
that they are adequately protected with overlying fascia, tissue or other protective barriers. Exposed tendon, nerves or
blood vessels should be protected by moving available muscle or fascia over them or by a layer of synthetic material.
Greater care should be taken with respect to weakened, irradiated or sutured blood vessels or organs. Bone fragments or
sharp edges could puncture a dressing barrier, vessel or organ.Wounds with enteric stula require special precautions in
order to optimize therapy.
1.4 Additional Precautions
• Debrillation: Remove the Cardinal Health™ NPWT Dressing if debrillation is required in the area of dressing
placement. Failure to remove the dressing may inhibit electrical current transmission and/or patient resuscitation.
• Magnetic Resonance Imaging (MRI): The Cardinal Health™ NPWT PRO family of devices is not MRI-compatible.
Do not take the device into the MRI area.
• Hyperbaric Oxygen Therapy (HBO): NEVER allow a device—whether on or o—inside a hyperbaric chamber.
The device must be disconnected from the patient prior to HBO treatment.
• Large Canisters: Use of Large Canisters (>500ml) may increase serious risks associated with excessive uid loss.
Monitor patient status continually.
• DO NOT USE for infants or other patients with low uid volume, nor for patients at high risk of major hemorrhage.

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Patient User Manual
• During Negative PressureWound Therapy, the Cardinal Health™ NPWT PRO family of devices and Cardinal Health™
NPWT Dressing are a closed system and are NOT vented to atmosphere.
• During Negative PressureWound Therapy, when a canister lls with uid, it should be replaced immediately as
uids such as wound exudate will not be removed from the dressing once the canister is full.
1.5 Safety Tips
KEEP THERAPY ON
The Cardinal Health™ NPWT PRO family of devices should be operated at least 22 hours out of every 24 hour period.
Contact your Healthcare Professional if therapy stops or if the device is OFF for more than 2 hours in a 24 hour period.
Your Healthcare Professional will need to change your dressing.
MONITORING THE WOUND
Inspect the dressing frequently to ensure that the foam is collapsed and that therapy is being delivered in a consistent
manner. Monitor wound exudates for signs of active bleeding. Monitor periwound tissue and exudate for signs of infection
or other complications.* Extra care and attention should be given if there are any signs of possible infection or related
complications. Infection can be serious.With or without the Cardinal Health™ NPWT PRO family of devices, infection can
lead to many adverse complications including pain, discomfort, fever, gangrene, toxic shock, septic shock, and various other
complications.With signs of more serious complications of infection, discontinue the use of the Cardinal Health™ NPWT PRO
family of devices until the serious infection is diagnosed and properly treated.
CARDINAL HEALTH™ NPWT DRESSING USE
Your Healthcare Professional will apply and change your dressings for you. The Cardinal Health™ NPWT Dressings
distributed by Cardinal Health are to be used exclusively with the Cardinal Health™ NPWT PRO family of devices.
NOTE: All dressing components of the Cardinal Health™ NPWT Dressing kit are packaged sterile.The decision to use clean
versus sterile/aseptic technique is dependent upon wound pathophysiology and physician/clinician preference.
All components of the Cardinal Health™ NPWT PRO disposable set are made without natural rubber latex.
Be sure to comply with all other 1.2 CONTRAINDICATIONS and 1.3 PRECAUTIONS for the Cardinal Health™ NPWT PRO
family of devices.
* Signs of possible infection may include fever, tenderness, redness, swelling, itching, and rash, increased warmth in the
wound area, sudden increase in pain, purulent discharge or a strong odor. Nausea, vomiting, diarrhea, headache, dizziness,
fainting, sore throat with swelling of the mucous membrane, disorientation, high fever (>102°F, 38.8°C), refractory
hypotension, orthostatic hypotension, or periwound induration (a sunburn-like rash) may be added signs of more serious
complications of infection.

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Patient User Manual
2. Introduction to the Cardinal Health™ NPWT
PRO Family of Devices
2.1 Getting to know the Cardinal Health™ NPWT PRO family of devices
You may not need to use many of the buttons on the device, but it is important that you are familiar with what they are
and their location (see Figure 1).
NOTE: The Cardinal Health™ NPWT PRO family device will be virtually silent during normal operation with
a well-sealed dressing.
Power OFF
Canister Release
Pressure Setting
Clamp
Power / Charging Status
Battery Charging Port
Power ON / MUTE
Continuous / Intermittent Mode
Alarm Condition Display
Figure 1

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Patient User Manual
2.2 Charging the Battery
The Cardinal Health™ NPWT PRO family of devices has an internal battery that provides up to 24 hours of operation from
a single full-charge. When the battery is running low, an alarm will sound to let you know you must plug in the device
to charge the battery. See section 3.3 ALARM OPERATION of this manual for AlarmTroubleshooting.
1. Plug the device’s A.C. Adapter into a suitable wall outlet (100-240VAC, 50-60Hz)
2. Insert the power plug into the Battery Charging Port on the side of the device (Figure 2).
3. The device will continue to work when charging
The Cardinal Health™ NPWT PRO family of devices should only be used with the supplied A.C. Adapter. Use of an
incorrectly rated adapter could create a shock hazard for the patient and caregiver.
Figure 2
Battery Charging Port

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Patient User Manual
3. Operating Instructions
Carefully read the 1.3 PRECAUTIONS and 1.5 SAFETY TIPS in the 1. IMPORTANT USER INFORMATION section before
attempting to operate and adjust the Cardinal Health™ NPWT PRO family of devices.
WARNING: The Cardinal Health™ NPWT PRO family of devices should only be used with the supplied A.C. Adapter.
Use of an incorrectly rated adapter could create a shock hazard for the patient or caregiver.The part number for the
adapters can be found in the 6. REPLACEMENT PARTS section of this manual.
3.1 Power ON / OFF
The ON and OFF buttons are located on the front top of the control panel.The ON and
OFF buttons control the application of power to the device.
3.2 Power-Up Procedure
When turning ON the Cardinal Health™ NPWT PRO family of devices, this is what you should expect to happen.
1. Press the ON button. All LED indicators will sequentially illuminate during the power-on self-test.
2. Each time the device is turned on, the systems goes through an initialization sequence including the front panel LED
displaying a series of numbers and/or letters.
3. Upon turning ON the device, the dressing should slowly collapse indicating the presence of suction.
4. The Cardinal Health™ NPWT PRO family of devices should be operated at least 22 hours out of every 24 hour period.
Contact your Healthcare Professional if the device is OFF for more than 2 hours in a 24 hour period. Your dressing
must be changed.
3.3 Alarm Operation
Clearing an Alarm Condition
To clear an AlarmType, remedy the condition using the AlarmTroubleshooting table below. Once the condition is
corrected, the alarm will automatically reset. To manually reset AlarmType 1-3, turn the therapy device OFF then ON.
The alarm will clear when the power is cycled. AlarmType 4 cannot be manually reset by cycling power or Muted.
NOTE: Pressing the ON (MUTE) button after an alarm will silence the alarm for 5 minutes. Alarm condition 4
cannot be Muted or manually reset by cycling power.
NOTE: In the event of an emergency, please contact your treating physician, caregiver, or your local emergency responders.
NOTE: If an Alarm Condition persists and cannot be resolved, please contact Cardinal Health for further assistance.

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Patient User Manual
Alarm Troubleshooting
What you
see or hear
Problem What to do More Information
FLASHING “1”
“Low Pressure/Leak”
Single beep.
Device is making
more noise.
There is an air
leak in either the
dressing or the
tubing connections.
• Clamp the tubing.
• If Low Pressure/Leak ashing“1”and audible
alarm resets, there is a leak below the clamp –
often in the dressing. Reopen the clamp before
addressing the leak. Gently press around drape
to check for leaks.
If leak is found, patch with extra drape material.
• If Low Pressure/Leak ashing“1”and audible
alarm continues, there is a leak above the
clamp. Check tubing connection at the canister.
Check to ensure the canister is fully seated and
locked. Check for cracks in the canister or lid
separation. If found, replace the canister.
• Open the clamp.
The alarm will reset, the pressure light will stop
ashing, and the pump will become quiet after you
nd and seal the leak.
Leaks often occur over areas of moist skin, creases
or folds in skin, and wrinkles in the drape.They can
occur if the drape snags on clothes or bed sheets.
FLASHING “2”
“Canister Full”
Two-tone beep.
The canister is full. • Clamp the tubing.
• Turn device o by pressing the OFF button.
• Press the canister release button above the
canister and slide the full canister out. Cap and
dispose of properly. Slide new canister in, align
the short ports and click into place.
• Open the clamp and press the ON button
to resume therapy.
The canister full alarm begins when the
canister is 90% full, but the device will continue
to work until the canister completely lls.
If the Cardinal Health™ PRO family of devices are
placed on its front, uid entering the canister will
cause a false canister full alarm and the canister
must be changed.
FLASHING “3”
“Low Battery”
Three-tone beep.
The battery is low
and will run out in
about 30 minutes.
Plug in the device. Use only the power cord that came with the Cardinal
Health™ PRO family of devices.
When the device is getting power, a green light will
illuminate on the front of the device.
A yellow light below the green light will show that
the battery is charging. It will turn o once the
battery is fully charged.
FLASHING “4”
“Service Timer”
Four beeps every
10 seconds.
Device is ready
to be checked
and serviced.
Return device to your representative for service. This alarm cannot be Muted or manually reset by
cycling power.
Pressure Setting will
not change.
Pressure lock-out
is engaged.
Unlock the device. Ask your caregiver how to Unlock your device.
Device is quiet and
uid is not moving in
the tube.
This is NOT
a problem.
No action needed.
If you want to move the uid into the canister,
ask your Healthcare Professional if you can use
the intermittent mode.
When the dressing has a good seal, uid may be
removed from the wound and stay in the tubing.
The foam will be compressed normally and the
device will be quiet.
See directions below for switching to the
intermittent mode.
An amber light is
showing on the
front of the device
below the pressure
numbers.
This is NOT a
problem. The device
is operating in
intermittent mode.
No action needed. Intermittent mode maintains target pressure
for ve minutes and decreases to -25 mmHg
for two minutes.

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Patient User Manual
4. Care and Cleaning
Your Healthcare Professional will handle much of the care and cleaning needed for your NPWT system. Please
periodically check to make sure the device is working properly and look for signs that uid has entered into the device.
Also regularly inspect the AC adapter for any damage or unusual wear.
If the device is not working properly or is alarming, refer to the AlarmTroubleshooting guide in the 3.3 ALARM OPERATION
section of this manual or contact your Healthcare Professional for help. If the AC adapter is damaged, it must be replaced
immediately. Contact your Healthcare Professional for help.
WARNING: Avoid spilling liquid on any part of the therapy device. Liquids can cause corrosion when left on electronic
controls which can lead to failure. Component failure may cause the therapy device to operate erratically, possibly
causing a potential hazard to the patient or Caregiver.
WARNING: The Cardinal Health™ NPWT PRO family of devices should only be used with the supplied A.C. Adapter.
Use of an incorrectly rated adapter could create a shock hazard for the patient or caregiver and/or severely damage the device.
4.1 Disposal of Dressings, Canister and Other Disposables
Your Healthcare Professional should remove your dressings, tubings, clamps, used canisters and any other disposables.
Ask your Healthcare Professional what to do with a used canister you have changed yourself.
Dispose of all disposable components in accordance with local, state, and federal regulations.
4.2 Cleaning the Device
The Cardinal Health™ NPWT PRO family device should need only light cleaning. Make sure to unplug the device before
cleaning. The Battery will automatically provide power so therapy is not interrupted. Clean the device with a damp soft
cloth and a mild soap and water solution.
Do not saturate the device with liquid or allow liquid to pool on the device. This can present a potential hazard for you
and/or your Healthcare Professional.
4.3 A.C. Power Adapter Inspection
The A.C. Adapter should be inspected regularly for damage and/or unusual wear. Replace damaged or worn Power
Supplies immediately. A.C. Adapters are available from Cardinal Health.
WARNING: The Cardinal Health™ NPWT PRO family of devices should only be used with the supplied A.C. Adapter. Use of an
incorrectly rated adapter could create a shock hazard for the patient or caregiver and/or severely damage the device.
WARNING: Avoid spilling liquid on any part of the therapy device. Liquids can cause corrosion when left on electronic
controls which can lead to failure. Component failure may cause the therapy device to operate erratically, possibly
causing a potential hazard to the patient or Caregiver.

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Patient User Manual
5. Specications
Cardinal Health™ NPWT PRO family of devices
Dimensions............................................................................................................. 6 x 4.3 x 2.75 in. (19.3 x 11.0 x 7.0 cm)
Weight.......................................................................................................................................................0.9 Lbs (0.43Kg)
Therapy Settings.....................................................................................................................50, 75, 100, 125, 150 mmHg
CanisterVolume...............................................................................................................................................300cc/500cc
With respect to electric shock, re, and mechanical hazards, conforms to IEC60601-1.
IEC Classification
• Medical Equipment
• Equipment not suitable for use in presence of ammable anesthetic mixture with air, oxygen, or nitrous oxide.
• Continuous Operation
• Type B Applied Part
• Class II Internally Powered Equipment
• IPXO
Battery
Duration (Fully Charged)...............................................................................................................................up to 24 hours
Electrical
External Power Supply Input.....100-240VAC, 50-60Hz, 200 mA or 12-24VDC, 850 mA (Optional)
External Power Supply Output ......................................................................................................................5VDC, 1 Amps
Patient & Enclosure leakage Current .......................................................................................................< 100 Micro amps
Environmental Conditions
Storage Conditions
Temperature Range................................................................................................................. 10°F (-12°C) to 110°F (43°C)
Relative Humidity Range ..........................................................................................................20 – 95% Non-condensing
Atmospheric Pressure Range....................................................................................................................50 kPa to 110 kPa
Operating Conditions
Temperature Range.......................................................................................................................40°F (4°C) to 90°F (32°C)
Relative Humidity Range ...........................................................................................................20 - 75% Non-condensing
Atmospheric Pressure Range....................................................................................................................50 kPa to 110 kPa
Service life ............................................................................................................................................................... 3 years
CAUTION: Federal law restricts this device to sale by or on the order of a physician.

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Patient User Manual
5.1 Explanation of Symbols
Class II, Internally
Powered Equipment
Type B Applied Part
Consult Instructions for Use
Not protected
against the harmful
effects of water
IPXO
Alternating Current
Expiry Date
Date of Manufacture
Manufacturer
Lot/Batch Number
Fragile
Keep Dry
Method of Sterilization --
Ethylene Oxide
Storage Conditions
Rx Only
Authorized Representative
in the European Union
Serial Number
Catalog Number
A.C. Power Status
Battery Charge Status
Continuos/Intermittent
Power OFF
Power ON/MUTE
Adjustment Button. UP.
Adjustment Button. DOWN.

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Patient User Manual
5.2 Electromagnetic Compatibility
The Cardinal Health™ NPWT PRO family of devices conforms to all pertinent requirements of IEC 60601-1-2.
The EMC summary tables are provided herein below for your reference.
Emissions Test
Harmonic emissions
IEC 61000-3-2
Guidance and Manufacturer’s Declaration: Electromagnetic Emissions (IEC 60601-1-2)
Class A
Complies
Complies
The PRO is suitable for use in all establishments,
including medical facilities, domestic establishments
and those directly connected to the public low-voltage
power supply network that supplies buildings used
for domestic purposes.
The PRO is not suitable for interconnection
with other equipment.
Voltage uctuations /
icker emissions
IEC 61000-3-3
RF emissions
CISPR 14-1
Compliance Electromagnetic Environment
Output Power of
Transmitter in watt(s) 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5GHz
Recommended separation distance between portable and
mobile RF communications equipment and the PRO.
Separation distance according to frequency of transmitter in meter(s)
0.01
0.1
1
10
100
0.12
0.38
1.2
3.8
12
0.12
0.38
1.2
3.8
12
0.23
0.73
2.3
7.3
23
The PRO is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of the PRO can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and the PRO as recommended
below, according to the maximum output power of the communications equipment.
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: At 80MHz and 800MHz, the separation distance for the higher frequency range applies Note:These guidelines
may not apply in all situations. Electromagnetic propagation is aected by absorption and reection from structures,
objects, and people.

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Patient User Manual
Immunity Test
Guidance and Manufacturer’s Declaration: Electromagnetic Immunity (IEC 60601-1-2)
IEC 60601
Test Level
Compliance Level
±6 kV contact
±8 kV air
±2 kV for power supply lines
±1 kV for input/output
±1 kV
line to line
±2 kV
line to earth
<5 % UT
(>95 % dip in
UT) for 0.5 cycle
3 A/m
40 % UT
(60 % dip in
UT) for 5 cycles
70 % UT
(30 % dip in
UT) for 25 cycles
<5 % UT
(95 % dip in
UT) for 5 sec.
±6 kV contact
±8 kV air
±2 kV for power supply lines
±1 kV for input/output
±1 kV
line to line
±2 kV
line to earth
<5 % UT
(>95 % dip in
UT) for 0.5 cycle
3 A/m
40 % UT
(60 % dip in
UT) for 5 cycles
70 % UT
(30 % dip in
UT) for 25 cycles
<5 % UT
(95 % dip in
UT) for 5 sec.
Floor should be wood, concrete, or ceramic tile. If oors are covered with
synthetic material, the relative humidity should be at least 30%.
Mains power quality should be that of a typical commercial and/or hospital
environment.
Mains power quality should be that of a typical commercial and/or
hospital environment.
Mains power quality should be that of a typical commercial and/or hospital
environment.
Power frequency magnetic elds should be at levels characteristic of a typical
location in a typical commercial or hospital environment.
Electromagnetic Environment
-
Guidance
Electrostatic discharge
(ESD) IEC 61000-4-2
Electrical fast transient/
burst
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and voltage
variations on power supply
IEC 61000-4-11
Power frequency (50/ 60
Hz) magnetic eld IEC
61000-4-8
Note: UTis the A.C. mains voltage prior to application of the test level.
Immunity Test
Guidance and Manufacturer’s Declaration: Electromagnetic Immunity (IEC 60601-1-2)
IEC 60601
Test Level
Compliance Level
3V rms
3V/m
3V rms
150 kHz ~ 80
MHz
3V/m
800 MHz ~ 2.5
GHz
Portable and mobile RF communications equipment should be used no closer to any part of the PRO including
cables, than the recommended separation distance calculated from the equation appropriate to the frequency
of the transmitter.
Recommend separation distance
d= 1.2 √P
d= 1.2 √P80 MHz to 800 MHz
d= 2.3 √P800 MHz to 2.5 GHz
where Pis the maximum output power rating of the transmitter in watts (W) according to the transmitter
manufacturer and dis the recommended separation distance in meters (m).
Field strengths from xed RF transmitters as determined by an electromagnetic site survey,
 should be less than the compliance level
in each frequency range.
Interference may occur in the vicinity of equipment marked with the following symbol:
Electromagnetic Environment
-
Guidance
Conducted RF IEC 61000-4-6
Radiated RF IEC 61000-4-3
Note1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note2:These guidelines may not apply in all situations. Electromagnetic propagation is aected by absorption and reection from structures, objects, and people.
 Field strengths from xed transmitters, such as base stations for radio (cellular/ cordless) telephones and land mobile radio, AM and FM radio broadcast, andTV broadcast cannot be predicted theoretically
with accuracy.To assess the electromagnetic environment due to xed RF transmitters, an electromagnetic site survey should be considered. If the measured eld strength in the location in which the PRO
is used exceeds the applicable RF compliance level above, the PRO should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as
reorienting or relocating the PRO.
Over the frequency range 150 kHz to 80MHz, eld strengths should be less than 3V/m.

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Patient User Manual
6. Replacement Parts
Cardinal Health™ NPWT PRO family of devices
Cardinal Health™ NPWT PRO device.......................................................................................................................6708888
Cardinal Health™ NPWT PRO to GO device..............................................................................................................47-0010
Power Supply
A.C. Power Adapter ................................................................................................................................................47-9100
Dressings
Cardinal Health™ NPWT Small Foam Dressing Kit (10 per case) .............................................................................47-1702
Cardinal Health™ NPWT Medium Foam Dressing Kit (10 per case).........................................................................47-1701
Cardinal Health™ NPWT Large Foam Dressing Kit (10 per case)..............................................................................47-1700
Cardinal Health™ NPWT X-Large Foam Dressing Kit (10 per case)..........................................................................47-1703
Cardinal Health™ White Foam Dressing (10 per case).............................................................................................47-1751
Canisters
Cardinal Health™ Disposable Canister with Gel, 300 cc (10 per case)......................................................................47-4000
Cardinal Health™ Disposable Canister with Gel, 500 cc (10 per case)......................................................................47-4500
Accessories
Cardinal Health™ NPWT PRO I.V. Pole Holder .........................................................................................................47-5600
Cardinal Health™ NPWT PRO Carrying Bag.............................................................................................................47-9600
Cardinal Health™ SpeedConnect™ Tubing ..............................................................................................................47-2000
Cardinal Health™ NPWT“Y”Connector...................................................................................................................47-2500
Cardinal Health™ Polyurethane Drape (10 per pkg.)...............................................................................................47-7000
Cardinal Health™ SensiSkin™ Drape (10 per pkg.)..................................................................................................47-7100
NOTE: In order to assure the highest safety, quality and ecacy of the products, the Cardinal Health™ NPWT PRO family
of devices should only be used with the Cardinal Health™ disposables, and Cardinal Health™ NPWT Dressings should
only be used with the Cardinal Health™ NPWT PRO family of devices.

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Patient User Manual
7. Questions & Information
For questions, comments or additional information pertaining to the Cardinal Health™ NPWT PRO family of devices,
please contact your local Cardinal Health representative, or:
Call our customer support professionals at 1.866.484.6798
Cardinal Health
Waukegan, IL 60085
www.cardinalhealth.com
[e-mail]
Always consult a physician and product instructions for use prior to application.
Caution: Federal law restricts these devices to sale by or on the order of a physician.

Patient User Manual

Cat. 6708888, 47-0010
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