Veridian Healthcare 11-100 User manual

INSTRUCTION MANUAL • ENGLISH & ESPAÑOL
VH Suction Pump
Tabletop Aspirator System
Model 11-100
Model 11-110
Please read this instruction manual
completely before operating this unit.
3-YEAR 2-YEAR
3-YEAR
2-YEAR
1-YEAR
1-YEAR

2 • ENGLISH
Suction Pump
Motor Housing Air Filter 2x 4” Tube
Auto Adapter
(11-110 only)
6’Patient Tubing
(mouthpiece catheter
NOT included)
Collection Jar
with Lid
2-pc Power Cord
(5) Air Filters
Instruction Manual
Replacement Parts
Order Form
Stop!
Please ensure you have all of the following
components before using your device.
IF YOU ARE MISSING ANY PARTS, INCLUDING INSERTS OR
INSTRUCTION MANUALS, DO NOT RETURN TO PLACE OF
PURCHASE. CONTACT CUSTOMER CARE AT 8663261313.

ENGLISH • 3
INDEX
Manufactured for:
Veridian Healthcare
1175 Lakeside Drive
Gurnee, IL 60031
www.veridianhealthcare.com
Made in China
#93-1103 08/18
©2018 Veridian Healthcare, LLC
Toll-Free Customer Care Help Line: 1-866-326-1313
Monday – Friday 8:30 a.m. – 4:30 p.m. CST
Care & Safety Information .....................................................................................4-5
Introduction..................................................................................................................6
Indications for Use.......................................................................................................6
Product Features..........................................................................................................7
Set Up & Operation ................................................................................................8-9
Battery/Power Operation ...................................................................................... 10
Cleaning and Disinfection................................................................................11-12
Changing the Filter .................................................................................................. 13
Troubleshooting ....................................................................................................... 14
Warnings & Cautions. .............................................................................................. 14
Device Symbols Warnings ...................................................................................... 15
Electromagnetic Compatibility.......................................................................16-19
FCC Statement........................................................................................................... 20
Product Specications ............................................................................................ 21
Warranty ..................................................................................................................... 22
Instrucciones en Español..................................................................................23-44

4 • ENGLISH
IMPORTANT
SAFEGUARDS
CARE & SAFETY INFORMATION
NOTE: Read all instructions carefully before use. The following basic precautions are needed
when using an electrical product. Failure to read and observe all precautions could result in
personal injury or equipment damage.
Improper care or use of your suction pump may result in injury, damage to the unit or
ineective treatment. Following these instructions will ensure the nebulizer’s ecacy
and long life.
GENERAL CAUTIONS AND WARNINGS
• Never allow the suction pump to be used without adult supervision.
• Do not use the suction pump for anything except patient treatment as directed by a
physician. Do not use the suction pump in a manner inconsistent with these instructions.
• The suction pump is an electronic device, keep away from water to avoid electrical shock.
Do not immerse the unit in liquid and do not use while bathing. If the unit should fall into
water, do not reach for it without rst unplugging the unit.
• Do not use while driving.
• Unplug the unit before cleaning it and after each use. Do not leave the unit plugged in
when not in use.
• Use only the included power cord(s).
• Always ensure that the air vents are not blocked or obstructed in any way.
• Dropping the suction pump or causing other heavy impact may damage the unit and
aect proper operation.
• Do not expose the unit to direct sunlight, humid environments, extreme temperatures,
strong static electricity or electromagnetic waves.

ENGLISH • 5
IMPORTANT
SAFEGUARDS
CARE & SAFETY INFORMATION
• If the suction pump is not functioning correctly, if it makes unusual sounds, or if during
use the patient experiences pain or discomfort, immediately stop use.
• The patient tubing and catheter should be cleaned daily and replaced monthly during
regular use or at the prescribing physician’s instructions.
• Do not use the unit if it has been dropped to the ground, exposed to
extremetemperatures or high humidity, or damaged in any way.
• Do not disassemble the suction pump or attempt to repair it.

6 • ENGLISH
INTRODUCTION
INDICATIONS FOR USE
Thank you for purchasing Suction Pump Aspirator. Please read this instruction manual
completely before using your unit to ensure safe and eective use, as well as long life of the
product.
WARNING: Federal law allows suction pumps to be sold by a physician’s prescription
only. These devices should be used only at the direction of a doctor or healthcare
professional and should be used only as intended and described in this manual.
The Suction Pump Tabletop Aspirator System is intended to be used to remove infectious
materials from wounds or uids from a patient’s airway or respiratory support system.

ENGLISH • 7
PRODUCT FEATURES
Power Cord
Connection
(on back of
pump)
Tubing and Filter Set
Collection Canister Lid
Patient Tube
Connection Point
Collection Canister
6’Patient Tubing
Air VentsPower
Switch Pressure Gauge
Display Dial
Pressure
Adjustment
Dial
Carrying
Handle
Patient Tube
Connection
Port

8 • ENGLISH
SET UP & OPERATION
Before the rst use of the suction pump if the unit has not been used for an extended period
of time, it should be cleaned thoroughly as described in the Cleaning and Disinfection section
of this manual.
Assemble the tubing and lter set:
• Firmly push the 4”tubing onto each end of the lter. The tubing
should t tightly onto the lter. If the tubing is not snug, then
the set should be replaced.
• Tubing/lter set should be left unassembled when not in use to
prevent any moisture build up in the tube or lter.
Assemble the tubing and lter set:
1. Replace the lid on the collection canister. The jar lid will not lock or fasten to the canister
but should t snugly and securely; take care when transporting liquid.
2. Place the canister into the open ring on the suction pump body.
3. Attach the tubing/lter set to the suction pump body, then securely attach the
6’ length patient tubing to the port on the collection canister lid.

ENGLISH • 9
SET UP & OPERATION
Always inspect the tubing and mouthpiece (not included) for cracks or wear prior to use and
replace as necessary.
Patient use:
1. Place the suction unit on a at, stable surface within operating range of the patient
and an electrical outlet. Ensure that the air vents on the side of the unit housing are not
blocked or obstructed.
2. Plug the power cord into the electrical
outlet.
3. Press the power switch to turn the unit on
and activate the suction operation.
4. Verify the suction unit is at the desired
suction level prior to patient suction by
turning the adjustment knob until the
required level is reached. The prescribing
physician can advise and explain what level
is necessary for the specic patient’s care.
NOTE: This device does not include the
patient catheter (commonly called suction
tip or pipette) as this piece is meant to be
replaced frequently. Consult your physician for advice and information on obtaining the
patient catheter.
5. When complete, turn the unit o and unplug it from the outlet if it will not be used again
for a period of time.
6. Dispose of the contents following the directions of the prescribing physician.
7. Follow the Cleaning and Disinfection directions as advised in this manual.

10 • ENGLISH
BATTTERY/ POWER OPERATION
The Suction Pump Tabletop Aspirator System is oered with two power option models — 2
piece DC Power Adapter; model 11-110 is rechargeable and includes an auto adapter.
Use common sense electric device caution when operating this unit. Always turn o the
power and unplug the device before cleaning or if the unit is not working properly.
• The included power cord should be plugged into the back of the suction pump unit.
• unplug the power cord from the wall and unit when the suction pump is not in use.
Rechargeable DC Power (11-110)
• This unit can operate by the internal rechargeable battery or under AC power.
• The included 2-piece power cord can be plugged into the unit for use or to charge the
device. The auto-adapter is intended for charging the internal battery on the go; do not
use this product while driving.
• Assemble the power cord and plug it into the unit prior to plugging into a standard wall
socket. Operating the unit while plugged into a wall socket will not aect the charged
battery life remaining on the internal battery.
• Charge time from expired battery: 8 hours.
• Charged battery life: 60 minutes at normal use; 50 minutes at maximum vacuum ow.

ENGLISH • 11
The patient tubing and mouthpiece (not included) should be thoroughly cleaned after each
use and disinfected each day when being used frequently unless a dierent cleaning regimen
is specied by your healthcare professional; additional hygienic precautions may be required
for use with high-risk patients. Always follow the direction of your healthcare provider.
Cleaning After Each Use:
1. Ensure that the power cord is disconnected from the power outlet.
2. Disconnect the air tube, lter, tube set and mouthpiece (not included). Remove the
collection canister and dispose of its contents. Do not wash or submerge the suction
pump body.
3. Wash and rinse all pieces in hot water, using a mild, non-abrasive detergent.
4. Allow all pieces to air dry completely, or dry them thoroughly with a clean, soft towel. Do
not store any parts wet as remaining moisture creates a risk of bacterial growth.
5. Occasionally wipe the body of the unit with a damp cloth and allow it to air dry. Only
clean the body of the unit when it is unplugged and completely cool.
Never use soap pads or powder cleanser to clean any part of the unit. Never use any cleaning
products that may be harmful when swallowed or inhaled.
It is recommended that air lter and tubing and collection canister be replaced
regularly depending on the frequency of therapy treatments or when damaged,
cracked or holes appear in the tubing. To order replacement parts, use the included order
form, call Customer Care at 866-326-1313 or contact your local dealer.
CLEANING & DISINFECTION

12 • ENGLISH
CLEANING & DISINFECTION
Disinfection at the End of Day / Treatment Period:
The suction pump should be disinfected once daily, after the last use of the day, unless a
dierent disinfection regimen is specied by a healthcare professional. Disinfect the suction
pump as follows:
1. Ensure that the power cord is disconnected from the power outlet.
2. Disconnect the air tube, lter, tube set and mouthpiece (not included). Remove the
collection canister and dispose of its contents. Do not wash or submerge
the suction pump body.
3. Wash all parts in hot water, using a mild, non-abrasive detergent.
4. Submerge all parts in a solution of one part white vinegar and three parts
distilled water for a minimum of 30 minutes.
5. Rinse all pieces thoroughly with water.
6. Allow all pieces to air dry completely, or dry them thoroughly with a clean,
soft towel. Do not store any parts wet as remaining moisture creates a risk
of bacterial growth.

ENGLISH • 13
CHANGING THE FILTER
• Never operate the unit without a lter.
• Under regular use, replace the lter monthly, or sooner if it turns gray, appears
contaminated is blocked or becomes wet.
• Use only Veridian Healthcare lters; additional lters are available for order using the
included order form, calling Customer Care at 866-326-1313 or contacting your local
dealer.
• Do not substitute cotton or any other materials for the lters.
• Do not attempt to clean the lters or reuse a lter.
To replace the lter, follow these steps:
1. Change the lter only when the unit is o, unplugged and completely cool.
2. Gently pull the lter cap out of the compressor.
3. Remove the lter from the lter cap.
4. Place a new lter in the lter cap.
5. Return the lter cap to its place, ensuring that it is rmly in place.

14 • ENGLISH
TROUBLESHOOTING
WARNING AND CAUTIONS
The unit will not turn on.
Check all power connections and ensure the cord is rmly plugged into the unit and wall
socket. Allow the rechargeable unit sucient time to recharge or operate with the power cord
plugged into the wall socket.
The motor is running, but there is no vacuum pressure.
Check that the tube connections are secure and that there are no leaks or cracks in the tubing.
Increase the vacuum level with the pressure adjustment dial.
There is very little vacuum pressure.
Increase the vacuum level with the pressure adjustment dial.Check that the tube connections
are secure and that there are no leaks or cracks in the tubing.
FOR ASSISTANCE IN TROUBLESHOOTING ADDITIONAL ISSUES, PLEASE CONTACT
CUSTOMER CARE AT 866-326-1313
Suction Pump Aspiration is intended for use as prescribed by physician for an
individual patient in medical applications only.
Use common sense electrical caution when operating the device. The VH Suction Pump
Tabletop Aspirator System runs on AC power or DC rechargeable battery. Always turn o the
power and unplug the device before cleaning or if the unit is not working properly.
Never attempt to disassemble the device or service a non-working device. Contact
Veridian Healthcare Customer Care department at 866-326-1313 for assistance in warranty
repair and service on your unit.

ENGLISH • 15
These symbols may appear on your device, instructions or packaging and may vary by make
and model.
Read This Manual—All included manuals should be read prior to rst use.
Warning—Symbol indicates a warning, prohibition or mandatory action that
mitigates a risk that is not necessarily obvious to the device operator.
Type BF Applied Parts—Indicates that a part of this unit comes in contact with the
patient in order to carry out it’s intended function.
Environment Protection—dispose of this product properly; consult with your local
recycling ordinances for proper recycling and disposal.
Keep Dry—This device should be kept dry; never submerge the unit. Consult with
the Care and Maintenance section of this manual for information on cleaning your
monitor.
Double Insulation—This unit is double-protected and thus to protection class 2.
Symbol Meaning

2012

2012
DEVICE SYMBOLS WARNINGS

16 • ENGLISH
ELECTROMAGNETIC COMPATIBILITY
Table 1
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration - electromagnetic emissions
This monitor is intended for use in the electromagnetic environment specied below.
The customer or the user of this monitor should assure that it is used in such an environment.
Emmission Test Compliance Electromagnetic Environment Guidance
Group 1
Class B
Class A
Complies
This monitor 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.
This monitor is suitable for use in all establishments, including domestic
establishments and those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic purposes.
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage uctuations/
icker emissions IEC
61000-3-3

ENGLISH • 17
ELECTROMAGNETIC COMPATIBILITY
Table 2
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration - electromagnetic immunity
This monitor is intended for use in the electromagnetic environment specied below.
The customer or the user of this monitor should assure that it is used in such an environment.
Electrostatic discharge
(ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
Power frequency
(50/60 Hz)
magnetic eld
IEC 61000-4-8
± 6 kV contact
± 8 kV air
± 2 kV for power supply lines
± 1 kV for input/output lines
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
<5 % UT
(>95 % dip in UT)
for 0.5 cycle
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 s
3 A/m
± 6 kV contact
± 8 kV air
± 2 kV for power supply lines
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
<5 % UT
(>95 % dip in UT)
for 0.5 cycle
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 s
3 A/m
Floors 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 or hospital environment.
Mains power quality should be that of a typical
commercial or hospital environment.
Mains power quality should be that of a typical
commercial or hospital environment. If the user of
this monitor requires continued operation during
power mains interruptions, it is recommended that
this monitor be powered from an uninterruptible
power supply or a battery.
Power frequency magnetic elds should be at
levels characteristic of a typical location in a typical
commercial or hospital environment.
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance

18 • ENGLISH
Table 3
For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacturer’s declaration - electromagnetic immunity
This monitor is intended for use in the electromagnetic environment specied below.
The customer or the user of this monitor should assure that it is used in such an environment.
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
NOTE 1 At 80 MHz and 800 MHz, 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.
* Field strengths from xed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio,
AM and FM radio broadcast and TV 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 this monitor is
used exceeds the applicable RF compliance level above, this monitor should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as re-orienting or relocating this monitor.
** Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3V/m.
3 Vrms 150 kHz to 80 MHz
3 V/m 80 MHz to 2,5 GHz
3 Vrms
3 V/m
Portable and mobile RF communications equipment
should be used no closer to any part of this monitor,
including cables, than the recommended separation
distance calculated from the equation applicable to the
frequency of the transmitter.
Recommended separation distance:
80 MHz to 800 MHz
800 MHz to 2,5 GHz
Where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is 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:
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance
1
d = 2.
1
d = 2.
d = 2.3
ELECTROMAGNETIC COMPATIBILITY

ENGLISH • 19
Table 4
For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Recommended separation distances between portable and mobile RF communications equipment and this monitor
This monitor is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The
customer or the user of this monitor can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and this monitor as recommended below,
according to the maximum output power of the communications equipment.
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
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be determined
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.
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
1
d = 2.
1
d = 2.
d = 2.3
Rated maximum
output
power of
transmitter
W
ELECTROMAGNETIC COMPATIBILITY

20 • ENGLISH
FCC STATEMENT
IMPORTANT INFORMATION REQUIRED BY THE FCC
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two
conditions: (1) this device may not cause harmful interference; and (2) this device must accept
any interference received, including interference that may cause undesirable operation.
NOTE: This equipment has been tested and found to comply with the limits for a Class B digital
device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable
protection against harmful interference in a residential installation. This equipment generates,
uses, and can radiate radio frequency energy, and if not installed and used in accordance with
the instructions, may cause harmful interference to radio communications. However, there
is no guarantee that interference will not occur in a particular installation. If this equipment
does cause harmful interference to radio or television reception, which can be determined by
turning the equipment o and on, the user is encouraged to try to correct the interference by
one or more of the following measures:
Reorient or relocate the receiving antenna.
Increase the separation between the equipment and receiver.
Connect the equipment into an outlet on a circuit dierent from that to which the receiver is
connected.
Consult the dealer or an experienced radio/TV technician for help.
CAUTION: Changes or modications not expressly approved by the party responsible for
compliance could void the user’s authority to operate the equipment.