Evenflo QuickAction User manual

Eveno® QuickAction™
Electric Nasal Aspirator
©2023 Eveno Company, Inc. 25701774 02/23
Read all instructions before
using this product.
KEEP INSTRUCTIONS FOR
FUTURE USE.

2
Introduction ................................................................................2
Warnings ...................................................................................3
Important Information Before Use .............................................3
Product Identication .................................................................4
Recharging the Battery ..............................................................4
Instructions for Use ....................................................................5
Cleaning and Disinfecting ..........................................................6
Technical Specications ............................................................7
Troubleshooting .........................................................................7
EMC Tables ...............................................................................8
FCC Interference Statement ...................................................11
Limited Warranty .....................................................................12
Table of Contents
Introduction
1. Only use the Eveno QuickActionTM Nasal Aspirator to
remove nasal secretions.
2. Soft Silicone Tip Design to reduce possibility of injury
during operation. Safe and comfortable for children.
3. Replaceable Tip: Bulbous and Cone-shaped tips available.
4. Compact and Lightweight.
5. Rechargeable Lithium Ion Battery
6. Rechargeable via USB-C Cable.
7. Easy Clean. Silicone tips and collection cup can be
removed and washed or boiled to disinfect.
8. Quiet. Low noise for nighttime use.
9. Soft Amber Night Light / Low Battery Indicator for use
in low light situations. When light is ashing, Nasal Aspirator
needs recharging.
NOTE: Use the Eveno QuickAction Nasal Aspirator to
remove nasal secretions under advice of your pediatrician.

3
WARNING!
• Product is intended to be used by adults.
• Product is intended to be used ONLY by adults.
• This is not a toy. DO NOT allow children to play with it.
• Keep away from children and pets. Small parts may be
inhaled or swallowed.
• Never immerse Nasal Aspirator main body in water.
• Never push the silicone tip too far into the child’s nostril.
• Always wash and dry the tip before and after each use.
• NEVER use in the child’s mouth or ears.
Important Information Before Use
The Eveno QuickAction Nasal Aspirator is designed to
provide intermittent suction for removal of nasal secretions and
mucus in children (age 0-12 years old) in a home environment.
WARNING!:
DO NOT modify this device. DO NOT expose the device to
extreme temperatures, very high humidity, or direct sunlight.
1. Avoid dropping the device.
2. Charge battery before rst use.
3. Low battery is indicated by the nightlight ashing (see pg. 4).
4. 3 green LED lights display when battery is fully charged.
5. The Eveno QuickAction Nasal Aspirator is for removing
nasal secretion only. Do not use this device other than for
the intended purposes.
6. For assistance with setup, use, or maintainance of this
device, please contact ParentLink at 1-800-233-5921.
7. Report any serious incidents involving this Nasal Aspirator
to Eveno by calling ParentLink at 1-800-233-5921.

4
Product Identication
1. Silicone Tip
2. Collection Cup
3. Night Light & Low Battery
Indicator
4. 3-Level Lighted Suction Indicator
5. Power Button
6. Main Body
7. USB-C Charging Port
8. USB-C Cable
1
6
8
5
4
2
3
1B
2 different size
silicone tips included
1A
7
Recharging the Battery
1. To recharge battery pack, use the included USB-C Cable.
2. Do not use a Nasal Aspirator that is damaged or modied.
3. Do not expose a battery pack or Nasal Aspirator to re or
excessive temperature. Fire or temperature above 265°F
(130°C) may cause an explosion.
4. Charging improperly at temperatures outside of the speci-
ed range may damage the battery and increase the risk of
re. -25°C~+55°C (-13°F~+131°F) with relative humidity up
to 85% (non condensing).

5
Instructions for Use
1. Choose the correct size included tip based on child’s age:
• Bulbous-shaped tip (1A) with the narrow opening:
recommended for children 0-2 years.
• Cone-shaped tip (1B) with the wider opening:
recommended for children 2+ years.
2. Attach the selected tip rmly to the Nasal Aspirator body;
it should t ush against the main body.
3. Press and release the power button to turn on. Test
the Nasal Aspirator on the back of your hand to ensure it
is activated and suctioning. The aspirator will continue to
suction for one minute and then will shut off automatically to
conserve battery life.
4. If selected to desired suction level, hold the child upright
and hold the Nasal Aspirator gently inside the child’s nostril
to begin suctioning to clear the mucus. Suction power is
mild and should only take a few seconds; consult your
pediatrician if child is uncomfortable.
5. The Nasal Aspirator has a soft amber night light for low
light situations that also acts as the low battery indicator.
When the light is ashing, the Nasal Aspirator needs to be
recharged.
NOTE: Mucus may not immediately be visible in the
collection cup. It is recommended that the silicone tip and
collection cup be removed and rinsed between each use to
keep any mucus from drying and clogging the device.
Suction Level Selection
1. The Nasal Aspirator is designed with 3 suction levels.
The suction level defaults to the last level used.
2. To change suction level, press and release the power button
to turn Nasal Aspirator on. Then press and hold power
button until desired suction level is reached (see pg. 4).
Repeat for next suction level.
NOTE: 1 light = low, 2 lights = medium, 3 lights = high

6
The following cleaning procedures should be
performed daily or when the device is being used
regularly. Failure to properly clean your unit may
result in clogging and shortened device life.
1. Carefully separate the silicone tip from the
collection cup.
2. Unscrew the collection cup from the device
main body.
3. Silicone tip and collection cup should be rinsed
well with hot water after each use to prevent
mucus from drying and clogging unit.
4. To Clean (at the end of the day / as needed):
Wash the collection cup and silicone tip with
mild, non-abrasive soap and water.
5. Disinfecting (after an illness / as needed):
After cleaning the pieces, rinse the tip and
collection cup thoroughly with hot water.
6. Do not wash or immerse the main body of the
aspirator. Use a soft, dry cloth to wipe Nasal
Aspirator. Never use abrasive cleaning agents
or any industrial strength cleaners.
7. Do not expose the device to extreme
temperatures, very high humidity, or direct
sunlight.
8. Avoid dropping the device.
9. Allow all parts to dry completely before
reassembly.
NOTE:
• Protect the Nasal Aspirator from drops or
heavy impact.
• Store in an area away from sunlight, dust
and humidity.
• If tips degrade or get damaged, please
replace them.
Cleaning and Disinfecting

7
• Effective Vacuum Pressure: Up to 65kPa (487 mmHg)
• Sound Pressure Level: < 60dB (30 cm away from the
device)
• Power supply: Rechargeable Lithium Ion Battery
• Charging: USB-C Cable
• Aspiration Tip: Soft Silicone
• Operating environment: 16°C~35°C (60.8°F~95°F) with
relative humidity up to 85% (non condensing)
• Storage/ Transportation environment: -25°C~+55°C
(-13°F~+131°F) with relative humidity up to 85%
(non condensing)
• Weight: approx. 4.9 oz (140.8g) with battery
• Product Dimensions with tip: approx. 7.36 in x 2.16 in x
1.4 in (18.7 cm x 5.5 cm x 3.5 cm)
Technical Specications
Troubleshooting
Problem Possible Cause Solution
The suction
is weak or
there is no
suction
Battery not charged Charge battery
The O-ring located
where the collection
cup screws in is
missing.
Make sure there is
an O-ring where the
collection cup screws into
the main body.
The collection cup
is not properly
screwed in.
Make sure the three
guides on each side of
the collection cup line
up with the guides on
the main body.
The Nasal
Aspirator is
clogged.
Wash collection cup and
silicone tip with mild, non-
abrasive soap and water.

8
60311000/NS15 is intended for use in the electromagnetic
environment specied below. The customer or the user of
60311000/NS15 must make sure that it is used in such an
environment.
Guidance and manufacturer's declaration - Electromagnetic
emissions
Phenomenon Professional
healthcare facility
environment a)
HOME
HEALTHCARE
ENVIRONMENT a)
Conducted and
radiated RF
EMISSIONS
a) CISPR 11
Group 1 Class B
Harmonic
distortion Not applicable
Voltage
uctuations and
ickering
Not applicable
a) The equipment is suitable for use in Home Health
Environments and Professional Health Care Environments
limited to patient rooms and respiratory treatment facilities in
hospital or clinics. The more restrictive acceptance limits of
Group 1 Class B (CISPR 11) have been considered and applied.
The equipment is suitable for use in the mentioned environments
when directly connected to the Public Mains Network.
b) The test is not applicable in this environment unless the ME
EQUIPMENT and ME SYSTEM used will be connected to the
PUBLIC MAINS NETWORK and the power input is otherwise
within the scope of the Basic EMC standard.
Guidance and manufacturer's declaration - Electromagnetic
immunity - Enclosure port
Phenomenon
Basic EMC
standard
or test
method
Immunity test levels
Professional
healthcare
facility
environment
HOME
HEALTHCARE
ENVIRONMENT
EMC Tables

9
EMC Tables
Proximity
elds
from RF
wireless
IEC 610004-3
COMPLIANT NOTE: Further
information about distances to
be maintained between portable
and mobile RF communications
equipment (transmitters) and
the 60311000/NS15 can be
requested from supplier using
the contact information provided
in this manual. However,
it is advisable to keep the
equipment at an adequate
distance of, at least, 0.5 m from
mobile phones or other RF
communications transmitters to
minimize possible interference.
RATED
power
frequency
magnetic
elds
IEC
61000-4-8 30 A/m c) 50 Hz or 60 Hz
a) The equipment is suitable for use in Home Health
Environments and Professional Health Care Environments
limited to patient rooms and respiratory treatment facilities
in hospital or clinics. The more restrictive IMMUNITY
acceptance limits have been considered and applied.
b) Before modulation is applied.
c) This test level assumes a minimum distance of at least
15 cm between the ME EQUIPMENT or ME SYSTEM and
sources of power frequency magnetic elds.
ELECTROSTATIC
DISCHARGE
IEC
61000-4-2
± 8kV contact
± 2 kV, ±4kV ±, ±8 kV,
±15 kV air
Radiated RF EM
elds IEC 61000-4-3 a)
10 V/m b)
80MHz - 2.7
GHz 80%
AM at 1kHz