ARJO HUNTLEIGH Flowtron Excel User manual

Flowtron Excel
Instructions for Use
...with people in mind
247933EN_0• /201

(i)
Contents
General Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . iii
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1
About this Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
About Flowtron Excel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Clinical Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3
Indications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Cautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Guidelines and Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
System Set Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5
Installing the Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Garment Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Garment Removal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
To Use Only One Garment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Pre-Use Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7
Start Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Shut Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Pressure Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8
Pressure Output Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Adjusting the Output Pressure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
System Calibration Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Decontamination . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
Routine Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
Flowtron Excel System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Flowtron Excel Pump. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Serial Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
Alarm Cancel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
Garments and Tubing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Technical Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13

(ii)

(iii)
General Safety
Before you connect the system pump to a mains socket, read carefully all the installation
instructions contained within this manual.
The system has been designed to comply with regulatory safety standards including:
• EN60601-1:1990/A13:1996 and IEC 60601-1:1988/A2:1995
• UL60601-1, UL2601-1 and CAN/CSA C22.2 No. 601.1-M90
• EN60601-1:2006 and IEC 60601-1:2005
• AAMI/ANSI ES60601-1:2006 and CAN/CSA C22.2 No.60601.1(2008)
Safety Warnings
• It is the responsibility of the care giver to ensure that the user can use this product
safely.
• Make sure that the mains power cable and tubeset or air hoses are positioned to
avoid causing a trip or other hazard, and are clear of moving bed mechanisms or
other possible entrapment areas.
• Electrical equipment may be hazardous if misused. There are no user-serviceable
parts inside the pump. The pump's case must only be removed by authorised
technical personnel. No modification of this equipment is allowed.
• The mains power socket/plug must be accessible at all times. To disconnect the
pump completely from the electricity supply, remove the plug from the mains
power socket.
• Disconnect the pump from the mains power socket before cleaning and inspecting.
• Keep the pump away from sources of liquids and do not immerse in water.
• Do not use the pump in the presence of uncontained flammable liquids or gases.
• Only the pump and garment/insert combination as indicated by ArjoHuntleigh
should be used. The correct function of the product cannot be guaranteed if
incorrect pump and garment combinations are used.
• The Flowtron®Excel system is NOT intended for use in the Home Healthcare
Environment (e.g. private dwellings or nursing homes).
WARNING - Portable RF communications equipment (including peripherals such as
antenna cables and external antennas) should be used no closer than 30cm (12 in) to
any part of the Flowtron Excel (ACS550), including cables specified by the
manufacturer. Otherwise, degradation of the performance of this equipment could
result.
Caution (applicable to the USA market only)
• US Federal law restricts this device to sale by or on the order of a physician.
Precautions
For your own safety and the safety of the equipment, always take the following precautions:
• Do not expose the system to naked flames, such as cigarettes, etc.
• Do not store the system in direct sunlight.
• Do not use phenol-based solutions to clean the system.
• Make sure the system is clean and dry prior to use or storage.

(iv)
Electromagnetic Compatibility (EMC)
This product complies with the requirements of applicable EMC Standards. Medical electrical
equipment needs special precautions regarding EMC and needs to be installed in accordance
with the following instructions:
• The use of accessories not specified by the manufacturer may result in increased
emissions by, or decreased immunity of, the equipment, affecting its performance.
• Portable and mobile radio frequency (RF) communications equipment (e.g. mobile/cell
phones) can affect medical electrical equipment.
• If this equipment needs to be used adjacent to other electrical equipment, normal
operation must be checked before use.
• For detailed EMC information contact ArjoHuntleigh service personnel.
Expected Service Life
The Flowtron Excel pump has an expected service life of seven years. To maintain the
condition of the pump have the pump serviced regularly according to the schedule
recommended by ArjoHuntleigh.
Do NOT use unapproved accessories or attempt to modify, disassemble or otherwise misuse
the Flowtron Excel system. Failure to observe this caution could result in injury, or in extreme
cases, death.
Environmental Protection
Incorrect disposal of this equipment and its component parts, particularly batteries or other
electrical components, may produce substances that are hazardous to the environment. To
minimise these hazards, contact ArjoHuntleigh for information on correct disposal.
Design Policy and Copyright
® and ™ are trademarks belonging to the ArjoHuntleigh group of companies. As our policy is
one of continuous improvement, we reserve the right to modify designs without prior notice.
The content of this publication may not be copied either whole or in part without the consent
of ArjoHuntleigh.
© ArjoHuntleigh 2017

1
1. Introduction
About this Manual This manual is your introduction to the Flowtron®Excel
system. You must read and fully understand this manual
before using the system.
Use this manual to initially set-up the system, and keep
it as a reference for day-to-day routines and as a guide to
maintenance.
If you have any difficulties in setting-up or using the
Flowtron Excel system, contact your local
ArjoHuntleigh sales office, listed at the end of this
manual.
Intended Use The intended use of this product is to prevent Deep Vein
Thrombosis (DVT). The garments are single patient use
only. It is not for use in the home healthcare
environment.
The Flowtron Excel system should be used as part of a
prescribed plan of care (refer to “Indications” on
page 3).
About Flowtron
Excel
The Flowtron Excel pump operates on a 60-second
automatically timed cycle consisting of approximately
12 seconds of inflation followed by approximately 48
seconds of deflation.
The Flowtron Excel system may be used on patients at
risk of developing deep vein thrombosis and in
conjunction with systemic interventions (e.g.
anticoagulation drugs) for the high risk patient.
The Flowtron Excel is intended for use ONLY in
Professional Healthcare Facilities (e.g. hospitals or
physicians’ offices).
A full technical description of the Flowtron Excel
system can be found in the Service Manual, part No.
SER0019, available from your local ArjoHuntleigh
sales office.

2
Flowtron Excel Pump - Front View
Mains Power Switch
Carry Handle Pressure Display
Garment
Pressure Control
Connectors
Single Leg
Mode Button
and Indicator

3
2. Clinical Applications
Indications The application of the Flowtron Excel system is for the
prevention of Deep Vein Thrombosis (DVT) when
combined with an individualised monitoring
programme.
This system represent one aspect of a DVT strategy; if
the patient's condition changes the overall therapy
regimen should be reviewed by the prescribing clinician.
The above are guidelines only and should not replace
clinical judgement.
Contraindications The Flowtron Excel system should not be used in the
following conditions:
1. Severe arteriosclerosis or other ischaemic vascular
diseases.
2. Known or suspected acute Deep Vein Thrombosis
(DVT) or phlebitis.
3. Severe congestive cardiac failure or any condition
where an increase of fluid to the heart may be
detrimental.
4. Pulmonary embolism.
5. Any local condition in which the garments would
interfere, including gangrene, recent skin graft,
dermatitis or untreated, infected leg wounds.
If you are unsure of any contraindications refer to the
patient’s physician before using the device.
Cautions 1. Proper garment application and connection to the
pump is essential.
2. Garments should be positioned in such a way that
they do not create any potential for constant
pressure points on the patient’s limb. Additional
care should be taken when placing the garments on
any deformed leg, or on legs with significant
oedema.
3. When used for DVT prevention, continuous
external pneumatic compression is recommended
until the patient is fully ambulatory. Uninterrupted
use of the Flowtron Excel system is encouraged.
4. Garments should be removed immediately if the
patient experiences tingling, numbness or pain, and
the physician notified.

4
5. The Flowtron Excel system should be USED
WITH CAUTION on patients with:
• Insensitive extremities.
• Diabetes.
• Impaired circulation.
• Fragile or impaired skin.
These are guidelines only and should not replace
clinical judgement and experience.
Guidelines and Recommendations
General
Recommendations
• While using the system, the patient’s limbs should be
checked during every shift, and more often if the
patient has known circulatory or skin problems, or is
diabetic.
• Clinical judgment should be used to determine if the
patient’s skin condition requires additional measures,
or if the treatment should be discontinued and
alternative modalities used.
• ArjoHuntleigh does not recommend the use of
compression stockings with its system. If these are
ordered by the physician, the clinician should ensure
that the compression stockings are properly
measured, applied and worn by the patient. Any
compression stocking used should be routinely
checked to ensure continued proper fit and
application, in addition to assessing the condition of
the skin.
• Where appropriate, patients should be instructed in
the proper use of the system, the purpose of therapy
and that any problems should be reported to the
nursing staff.
DVT Prophylaxis • The Flowtron Excel system should be applied to the
patient pre-operatively, prior to the induction of
anaesthesia.
• The system should be used continuously for no less
than 72 hours post-operatively or until the patient
becomes fully ambulatory.
• If the garment cannot be applied to the operative
limb during surgery, it may be applied to the limb
once the patient reaches the recovery unit.
In the non-surgical patient, the system should be
initiated immediately when the risk of DVT formation is
identified.

5
3. System Set Up
Installing the Pump Attach the pump to the bed frame using the bed bracket,
or place the pump on the floor under the bed.
Garment Application 1. Check that the mains power switch on the pump is
in the off (O) position.
2. Remove the garments from the packaging and
unfold.
Garments are for single patient use only. Do not
use the garments on a different patient after
treatment.
3. Place the back of the patient’s leg in the centre
section of the garment with the connector tubing
pointing downwards towards the foot.
4. Starting with the side of the garment that does not
have the Velcro1tabs, wrap securely against the
leg. While holding the garment against the leg,
wrap the tabs over the top. Ensure that the garment
is close-fitting and has no creases or folds. The
connector tubing should be pointing towards the
patient’s heel.
5. Make sure the tubing assembly is connected to the
garment connector on the pump.
6. Connect the garment connector to the tubing
assembly. Ensure that a sharp ‘click’ is heard. Pull
lightly to confirm proper connection.
7. Repeat steps 3 to 6 for the second garment, if used.
Garment Removal 1. To disconnect a garment, press on the tubing
assembly snap-lock connector and pull the garment
connector away from the tubing assembly.
To Use Only One
Garment
To use only one garment, connect a single garment to
either connector.
The snap-lock connectors on the pump are self-
sealing and do not require unused garments to
be attached.
1. Velcro®is a registered trademark of VELCRO USA Inc.

6
4. Pre-Use Check
Before powering on the Flowtron Excel system, ensure
that:
• The pressure control knob has been set to the mid
position marked 40 mmHg .
• Garments have been applied to the patient’s legs
correctly, close-fitting and without creases or
folds.
• There are no kinks in the tubing.
• The pump is connected to the mains power supply
but not switched on.
• All tubing connections are secure.
• The system has been arranged so that the power
cable and garment tubing do not pose a trip or
strangulation hazard.

7
5. Operation
Start Up Connect the pump to the mains power supply using the
power cable provided. Turn the mains power switch to
the on (I) position and it will illuminate green. The pump
performs a two-second self test cycle where the pressure
display, LEDs and alarm are tested. The pump then
proceeds directly to the inflation cycle.
The garments will inflate alternately. The first garment
inflates for approximately 12 seconds and is deflated for
approximately 48 seconds.
The second garment, if used, inflates 30 seconds after
the first garment has deflated and follows the same
inflation/deflation cycle.
If a single garment is attached, press the Single Leg
button to prevent the alarm system from indicating
a fault. The system responds with a ‘beep’ and the
yellow LED on the Front Panel illuminates.
If the Single Leg button is pressed while two
garments are connected, the system will
automatically reset to two-garment operation
after two single-garment inflation cycles.
Verify that the pressure display is indicating the desired
output pressure prescribed by the physician. Refer to
section “Pressure Adjustment” on page 8 for specific
pressure setting instructions.
If the operation or performance of the pump
changes during use, refer to “Troubleshooting”
on page 11 of this IFU before calling a service
engineer or contacting your local ArjoHuntleigh
sales office.
Loss of mains power will halt therapy.
Shut Down Turn the power switch to the off (O) position. Turning
the power off will stop the patient therapy.
If it is required to completely isolate the pump
from the mains power, remove the plug from the
mains power socket.
Disconnect and remove the garment(s) as required.
Garments are for single patient use only. Do not
use the garments on a different patient after
treatment.

8
6. Pressure Adjustment
The pressure control mechanism is located on the front
of the pump and ranges from 30-60mmHg. The pressure
exerted by the garments on the leg can be adjusted by
turning this knob. Turning the knob clockwise increases
the pressure; counterclockwise decreases the pressure.
The recommended pressure setting is 40 mmHg.
Alternatively, use the pressure prescribed by the
treating physician.
The Flowtron Excel pump pressure monitoring system
is independent of the pressure control and delivery
system, providing added reliability and safety. The
digital display indicates the actual pressure that is
delivered to the garments, and provides immediate and
continuous feedback regarding pump performance.
The pressure display is used for the following functions:
Pressure Output
Check
After turning the pump on, check that the pressure
display is showing the desired output pressure when the
garments are inflated. Visually recheck the display at
regular intervals.
Adjusting the Output
Pressure
If necessary, the pressure can be adjusted during the
active inflation period, by rotating the pressure control
knob until the desired pressure is displayed.
System Calibration
Check
To confirm the calibration accuracy of the pressure
control and display, perform the following check each
time the pump is turned on:
During normal operation when the pressure display
reads , the pointer on the pressure control knob
should be located within the 40 mmHg arc on the front
panel .
If the display reads 40 but the control knob is not within
the 40 mmHg arc, the pump should not be used and
referred to service for recalibration.

9
7. Decontamination
The following processes are recommended, but should be adapted to comply with
the local or national guidelines (Decontamination of Medical Devices) which may
apply within the Healthcare Facility or the country of use. If you are uncertain, you
should seek advice from your local Infection Control Specialist.
The Flowtron Excel pump should be routinely decontaminated between patients and
at regular intervals while in use, as is good practice for all reusable medical devices.
To clean Clean all exposed surfaces and remove any organic
debris by wiping with a cloth moistened with a simple
(neutral) detergent and water.
Do not allow water or cleaning solutions to collect on the
surface of the pump.
Chemical Disinfection We recommend a chlorine-releasing agent, such as
sodium hypochlorite, at a strength of 1,000ppm
available chlorine (this may vary from 250ppm to
10,000ppm depending on local policy and
contamination status).
Wipe all cleaned surfaces with the solution, then wipe
using a cloth moistened with water and dry thoroughly.
Alcohol based disinfectants (strength 70%) may be used
as an alternative.
Ensure the product is dry before storage.
If an alternative disinfectant is selected from the wide
variety available, we recommend that suitability for use
is confirmed with the chemical supplier prior to use.
WARNING
Remove the electrical supply to the pump by disconnecting the mains power
cable from the mains power supply before cleaning.
Protective clothing should always be worn when carrying out decontamination
procedures.
Caution
Do not use Phenol-based solutions or abrasive compounds or pads during the
decontamination process as these will damage the surface coating. Avoid
immersing electrical parts in water during the cleaning process. Do not spray
cleaning solutions directly onto the pump. Do not immerse the tubeset in
water.
Caution
Garments are single patient use and hence cannot be cleaned or reused.

10
8. Routine Maintenance
Flowtron Excel
System
Maintenance The equipment has been designed to be maintenance-
free between service periods.
Servicing ArjoHuntleigh will make available on request service
manuals, component parts lists and other information
necessary for ArjoHuntleigh trained personnel to repair
the system.
Service Period ArjoHuntleigh recommends that the Flowtron Excel
pump is serviced every 12 months by an ArjoHuntleigh
authorised service agent.
Flowtron Excel Pump
General Care,
Maintenance and
Inspection
Check all electrical connections and power cable for
signs of excessive wear.
Check the tubeset and connectors for any damage.
In the event of the pump being subjected to abnormal
treatment, e.g. immersed in water or dropped, the unit
must be returned to an authorised service centre.
Serial Labels The serial number for the pump is on the label on the
back of the pump case. Quote this serial number when
requesting service.

11
9. Troubleshooting
The Flowtron Excel system features an audible and visual alarm. If a problem
occurs, the system will sense the fault and briefly flash a message on the front panel
pressure display.
If the same fault continues for 10 successive inflations, the audible alarm will sound
and a flashing message will remain on the pressure display until corrective action is
completed.
The exception to this is an fault which will alarm immediately.
Alarm Cancel After a fault has been corrected, the alarm can be
cancelled by two methods:
1. Switch the pump off, then on again.
2. Allow the pump to run until it senses a normal
inflation; it will then reset itself.
Continue to watch the display for approximately one
minute after reset. If no flashing messages reappear, the
fault has been cleared.
If the troubleshooting procedures do not return
the system to normal performance, stop using the
system immediately and call the service engineer.
Display Problem Corrective Action
1. Hose disconnected at garment.
2. Garment leak.
3. Low pressure.
1. Check the hose connection at
garment end.
2. Check garment and replace if
faulty.
3. Call the service engineer.
1. Hose kinked causing a blocked
tube.
2. Hose disconnected at pump.
3. Single garment attached
without pressing ‘single leg’
button.
1. Check hoses for kinks or
obstructions.
2. Check the hose connection at
pump outlet.
3. Press ‘single leg’ button, if only one
garment to be used.
Pump failure. DO NOT USE PUMP.
Call the service engineer.
No displays,
no indications,
no operation
1. Power failure.
2. Fuse blown.
1. Check mains power supply.
Check power cable.
2. Call the service engineer.
Yellow LED on the top
panel flashes
(approximately 4 times
per second)
Internal electronic fault DO NOT USE PUMP.
Call the service engineer.

12
10. Accessories
GARMENTS AND TUBING
Description Garment
Part No. Size
Standard Calf Garment DVT10 Circumference up to 43cm (17”)
Calf Garment (Sterile) DVT10S Circumference up to 43cm (17”)
Large Calf Garment DVT20 Circumference up to 58cm (23”)
Standard Thigh Garment DVT30 Circumference up to 71cm (28”)
Thigh Garment (Sterile) DVT30S Circumference up to 71cm (28”)
Large Thigh Garment DVT40 Circumference up to 89cm (35”)
Extra Large Calf Garment DVT60L Circumference up to 81cm (32”)
Calf Garment L501-M Circumference up to 43cm (17”)
Thigh Garment L503-M Circumference up to 71cm (28”)
Connector Tubing L550
(SP057)
Length 150cm (60”)
Connector Tubing L552
(SP061)
Length 300cm (118”)

13
11. Technical Specification
If the pump is stored in conditions outside of the
“Operating” ranges, it should be allowed time to
stabilise at normal operating conditions before use.
Pump
Model: Flowtron Excel
Part Numbers: UK/AUS KSA USA
247003 - UK
247003AU - AUS
247004 (247EUR) - EU
247009KSA 247001
Supply Voltage: 230 V 230 V 120 V
Supply Frequency: 50 Hz 60 Hz 60 Hz
Power Input: 35 VA MAX 35 VA MAX 35 VA MAX
Size: 133 x 152 x 275 mm
Weight: 2.7 kg
Case Material: Fire Retardant ABS Plastic
Plug Fuse Rating: 5A BS1362 (UK ONLY)
Pump Fuse Rating: T1AL 250 V
Degree of protection
against electric shock:
Class II, Double Insulated with Functional Earth
Type BF
Degree of protection
against liquid ingress: IPX0 - No protection
Mode of operation: Continuous
Cycle or Therapy Modes: 60 seconds total
12 seconds inflation
48 seconds deflation
Pressure Range: 30 - 60 mmHg (±4 mmHg)
ENVIRONMENTAL INFORMATION
Condition Temperature Range Relative Humidity Atmospheric Pressure
Operating +10 °C to +40 °C
(+50 °F to +104 °F)
30% to 75%
(non-condensing)
700 hPa to 1060 hPa
Storage and Transport
(Long Term)
+10 °C to +40 °C
(+50 °F to +104 °F)
20% to 95%
(non-condensing)
700 hPa to 1060 hPa
Storage and Transport
(Short Term)
-20 °C to +50 °C
(-4 °F to +122 °F)
20% to 95%
(non-condensing)
500 hPa to 1060 hPa
Products should be well packaged and stored in a well-ventilated, dry and non-corrosive environment.

14
Symbols
The operator must read
this document
(Instructions for Use)
before use.
Note: This symbol is blue
on the product label.
O
(Off)
Power:
Disconnects from
the mains supply
Do not dispose of in
domestic refuse
With respect to electric
shock, fire and
mechanical hazards only
in accordance with CAN/
CSA-C22.2 No. 60601.1
(2008).
MEDICAL EQUIPMENT
I
(On)
Power:
Connects to the
mains supply
Type BF
Refer to this document
(Instructions for Use) for
a description of the
product classification (3rd
Edition).
SN: Serial Number REF: Model number
Refer to this document
(Instructions for Use) for
a description of the
product classification
(2nd Edition).
Fuse Double Insulated
Manufacturer: This
symbol is accompanied
by the name and the
address of the
manufacturer.
Guidance and manufacturer’s declaration - electromagnetic emissions
The pump is intended for use in the electromagnetic environment specified below. The customer or the
user of the pump should assure that it is used in such an environment.
Emissions Test Compliance Electromagnetic environment - guidance
RF emissions
CISPR - 11
Group 1 The pump uses RF energy only for its internal
function. therefore, its RF emissions are very low
and are not likely to cause any interference in
nearby electronic equipment.
RF emissions
CISPR - 11
Class B The pump 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.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Complies
i