ACeevac SUC 81025 User manual

ACeevac
High Vacuum High Flow
Portable Suction Pump
SUC 81025
220 240 V~ 50 Hz
User Manual
CLEMENTS
Manual No. SUC 81025 008
Issue 3

User Manual
ACeevac High Suction Pump
Manual Number SUC 81025 008 ssue 3 2021-02
Copyright © 2021 CU Medical Australia Pty Ltd
The information in this manual was originated by, and is the exclusive
property of CU Medical Australia Pty Ltd. t is furnished for customer
information only, and is not an authorisation or licence to make this
product or to furnish this information to others.
Safety
Thank you for purchasing this Clements ACeevac High
Suction Pump.
For your safety it is imperative that this unit only be
operated by authorised personnel in accordance with the
instructions as described in this manual. Operated in this
way, the ACeevac High Suction Pump will provide the
standard of service specified.
Due to continual improvements in product design, the
ACeevac High Suction Pump may vary in detail from the
descriptions in this manual. n the event of further
questions please contact your local distributor or CU
Medical Australia direct.
Familiarise yourself with these Directions for Use
before operating this device.
Sponsor:
CU Medical Australia Pty Ltd
Unit U, 10 - 16 South St
Rydalmere NSW 2116 Australia
Phone: [phone]
Website: www.clements.net.au
CA-M srl
Via Ugo La Malfa 13
Frazione Pilastro
43013 Langhirano (PR)
taly
0123

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Contents
Description......................................................................... 4
Specifications .................................................................... 5
Environmental Conditions .................................................. 6
Symbols. ..... ..... ..... ...... ..... ..... ..... ...... ..... ..... ..... ...... ..... ..... ... 7
Cautions ........ ..... ...... ..... ..... ..... ..... ...... ..... ..... ..... ...... ..... ..... 9
Controls and Operation.... ...... ..... ..... ..... ..... ...... ..... ..... ..... ... 10
sing FLOVAC Disposable Liners ..................................... 11
Cleaning .......... ..... ...... ..... ..... ..... ...... ..... ..... ..... ...... ..... ..... ... 13
Spare Parts........................................................................ 15
Troubleshooting ......... ..... ...... ..... ..... ..... ...... ..... ..... ..... ...... ... 16
Wiring Diagram..... ..... ..... ...... ..... ..... ..... ...... ..... ..... ..... ...... ... 17
Diagnostic Setup...... ...... ..... ..... ..... ...... ..... ..... ..... ...... ..... ..... 18
Periodic Safety Check.... ..... ...... ..... ..... ..... ...... ..... ..... ..... ..... 20
Return for Repair . ..... ..... ...... ..... ..... ..... ...... ..... ..... ..... ...... .... 20
Emissions Guidance Table ................................................ 21
Immunity Guidance Table .................................................. 22
Immunity Guidance Table ................................................. 23
Separation Guidance Table .............................................. 24
Warranty... ...... ..... ..... ..... ...... ..... ..... ..... ...... ..... ..... ..... ...... .... 26

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4 Description
Description
The Clements ACeevac High Suction Pump is a compact,
portable unit designed to suit the needs of hospitals, doctors’
surgeries and paramedics in providing a strong source of
suction for use in indoor environments where mains power is
available.
Identification
SUC 81025 ACeevac High Vacuum / High Flow Portable Suction
Pump
Intended Use
To provide a continuous vacuum source, within the stated
operating vacuum range, for the aspiration of fluids and
particulate matter in medical procedures carried out by
clinically trained and authorized personnel.
Contraindications
Before using the ACeevac, consult the instructions for use.
Failure to follow instructions in this manual could cause harm.
Do not use for thoracic or low vacuum drainage.
Do not use the ACeevac for suctioning of explosive, corrosive or
easily flammable fluids.
ACeevac is not suitable for MR . Do not place in the ACeevac
pump MR environments.
Pump Classifications
GMDN 63642
GMDN Term Surgical suc ion pump
GMDN Synonym Aspira or
Device Class Class IIa (Rule 11)
Elec rical Pro ec ion Class II
Pro ec ion Type BF Applied Par
S erilisa ion No supplied in s erile s a e
Anaes he ic Ra ing
NOT Ca egory AP
NOT Ca egory APG
Opera ion Mode Con inuous opera ion

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5
Specifications
Specifications
Maximum Vacuum -80 kPa [-600 mmHg]
Maximum Flow 21 L/min ( hrough jar) 32 L/min (free air)
Mains Power
Requiremen
220 - 240 V~ 50 Hz 110 VA
S a us Indica or Green neon lamp in On/Off swi ch indica es power
available s a us
Pump Pis on ype
Fil er Disposable hydrophobic and bac erial fil er
BFE 99.9999%, VFE 0.027 micron
Collec ion Con ainer 1 li re au oclavable, sha erproof plas ic jar
Op ional 2 li re au oclavable, sha erproof plas ic jar
Op ional 1 li re disposable liner jar
Op ional 2 li re disposable liner jar
Overfill Pro ec ion Floa valve mechanism
Vacuum Con rol Needle valve
Gauge Bourdon ube ype. Dual scale.
Gauge Range 0 o -100 kPa gradua ed a 5 kPa
0 o -760 mmHg gradua ed a 50 mmHg
Weigh 3.6 kg
Dimensions 360L x 215W x 195H mm
S andard
Condi ions
25°C, Sea level, 100kPa
Mo or PSC AC mo or
Fuse F1.6A L 250V
Jar Classifications
GMDN 44943
GMDN Term Suc ion Sys em Canis er, Reusable
Device Class Class I (Rule 1)
S erilisa ion No supplied in s erile s a e

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6 Environmental Conditions
Package Contents
The Clements ACeevac package contains:
• ACeevac portable suction pump
• Silicone 8 x 14 mm medical suction tubing; 18cm x2, 150cm x1
• 1 litre reusable collection jar with lid assembly
• 2-Pin AU plug to EC 320 power lead
• Disposable antibacterial/hydrophobic filter
• Stepped conical tubing connector
Environmental Conditions
Environmental conditions for operation, transportation and
storage are shown in the following table. n addition, for
vehicular transportation, the unit should be kept upright.
State Parameter Minimum Maximum
Opera ing Tempera ure 5ºC 35ºC
Humidi y 10% RH 93% RH
Barome ric Pressure 700 hPa 1060 hPa
Tempera ure -25ºC 70ºC
Humidi y 0% RH 93% RH
Barome ric Pressure 500 hPa 1060 hPa
Transpor and S orage
Al i ude 0 m 2000 m

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7
Symbols
General warning
Consul user manual
Type BF Applied Par (suc ion cannula)
Insula ion Class II (double insula ion)
Hz Mains power frequency
Off
CE Mark in conformi y wi h CE MEDDEV direc ive
93/42/EEC and subsequen changes
Manufac urer
REF Model / Reference Number
LOT Lo / Ba ch Number
On
~Al erna ing curren
Symbols
0123

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8 Symbols
SN Serial Number
Fragile
Rela ive Humidi y
Keep Cool / Keep ou of direc sunligh
Tempera ure Range
A mospheric Pressure Range
C-Tick Mark
Dispose of elec rical produc according o requiremen s
of WEEE direc ive
IP21
Degree of pro ec ion agains in rusion by body par s or
objec s an agains ingress by wa er.
1s Digi - Pene ra ion of Solids
2 = Pro ec ed agains solids > Ø 12.5 mm
2nd Digi - Pene ra ion of Liquids
1 = Pro ec ed ver ical dripping wa er
Symbols

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9
Cautions
Usage
1. Use only for the specified Intended Use.
2. Do not use near flammable substances such as oxygen or
anaesthetic gases.
3. Home care use is restricted to home carers and physically and
mentally competent adults.
4. n home care use, keep accessories out of reach of infants as
small parts can present a choking hazard.
Fluids
1. Keep device clear of water and other fluids. Do not handle pump
with wet hands.
Electrical
1. Use only the supplied power cord.
2. Confirm that electrical rating of rating label matches that of the
mains power. Avoid the use of power boards and extensions.
3. Maintain clear access to the mains power outlet to facilitate
disconnection.
4. Place pump clear of patient and other electronic equipment.
5. When not in use, disconnect from power supply.
6. Do not pull cable to remove plug from mains power outlet.
General
1. Check the pump and fittings for damage before each use.
2. Do not use without the bacteria/hydrophobic filter correctly
fitted.
3. Switch off pump immediately if overflow float valve is actuated.
4. After use, clean and store away from heat, dust and sunlight.
Cautions

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10
Operation
1. Place the pump on a flat stable horizontal surface.
2. Connect a short length of silicone tubing from the jar “VACUUM”
port to the “ N” (or directional arrow symbol) side of the
bacterial/hydrophobic filter. Connect a short length of silicone
tubing from the other side of the filter to the pump inlet.
3. Connect the long silicone tubing to the jar “PAT ENT” port.
4. Connect supplied power cord to power socket at rear of pump.
Connect power cord to compatible mains outlet.
5. Press switch to turn on pump. (Press again to turn off.)
Controls and Operation
Pump Controls
Bac erial / Hydrophobic Fil er
» Mus ALWAYS be fi ed «
Vacuum Con rol
“IN” or Δ Side
of Fil er
“VACUUM” por
(above floa valve)
ON / OFF
Rocker
Swi ch
Vacuum Gauge
“PATIENT” Por
Connec Pa ien
Tubing
Power Inle
(a rear)

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11
Using FLOVAC Disposable Liners
6. Occlude tubing and adjust vacuum control to the required
vacuum level. (Clockwise = increase)
Always reduce the vacuum level for paediatric and neonatal
patients.
7. Apply suction to patient with compatible suction cannula.
8. When finished, switch off pump by pressing switch.
Ensure that the mains power plug is accessible at all times when
pump is in use, in case a positive disconnection from the mains
power supply is required.
Using FLOVAC Disposable Liners
1. Remove liner from package and
extend liner from lid.
2. nsert liner bag [1] into the matching
size support jar [2].
Press edge of lid firmly all around
edge to ensure seal.
3. Close the TANDEM inlet [3] with the
attached cap [4].
4. Fit jar assembly into pump.
5. Press short end of yellow reusable
nipple [6] firmly into matching yellow
port [5] on the lid.
6. Push tubing from filter onto yellow
nipple [6].
7. Connect patient tubing to white inlet
elbow [7]. Connect patient tubing to
suitable suction cannula.
1
2
7
4
3
5
8
6
Note: For disposable jars only, that have a hydrophobic and
antibacterial filter built-in to the lid, connection may be made directly
to the pump inlet nipple.
For reusable jars, connection must be made through an inline
hydrophobic and antibacterial filter.

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12 Suction Accessories
Suction Accessories
The device and its accessories are biocompatible in accordance with
EN 60601-1.
Suction Cannulae
Suction cannulae or suction probes for contact with the human body
should comply with SO 10993-1 requirements for biocompatibility.
Collection Jar (Canister)
The mechanical strength of the reusable collection jar (canister) is
guaranteed for 30 cycles of cleaning and sterilization. Beyond this,
the there may be signs of decay and replacement is recommended.
Silicone Tubing
The number of cleaning and sterilization cycles of the silicone tubing
is dependent on the actual usage. Tubing should be checked for
cracking and other visible signs of wear before re-use.
Disposable Liner Disconnection
1. Switch off pump.
2. Disconnect white elbow together with patient tubing from
“PAT ENT” port and close port firmly with attached cap [8].
3. Disconnect yellow nipple [6] from “VACUUM” port [5].
4. Ensure that “TANDEM” port [3] is firmly closed with attached
cap [4].
5. Carefully remove liner from support jar using lid handle and
dispose of according to local protocols for potentially
biohazardous waste.

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13
Cleaning
Cleaning
After Each Operation
Empty Reusable Collection Jar
1. Switch off pump.
2. Disconnect tubing from jar “PAT ENT “ port.
3. Disconnect tubing from jar “VACUUM” port.
4. Carefully remove jar from pump and dispose of aspirated
fluid according to local protocols for potentially
biohazardous waste.
Clean
Housing
Wipe clean with a damp soapy cloth. Do not immerse or allow
liquid to enter the housing. Do not use abrasive cleaning agents.
Suction Tubing
Suction Tubing should be sterilised with sterilants determined by
local protocols and compatible with silicone tubing. Suction
tubing may be autoclaved to a maximum of 121°C for 15 minutes.
At higher temperatures the suction tubing will discolour and lose
shape.
Collection Jars
Place jars upright or up-side-down in autoclave - not on their
sides. Autoclave to a maximum of 121°C for 15 minutes. Do not
use phenolic solutions as disinfecting agents in polycarbonate
jars.
Lid
Unlock bayonet on float cage by rotating cage clockwise.
Disconnect float cage and float from lid and separate seal from lid.
Place all items upright or up-side-down in autoclave - not on
their sides. Autoclave all items to a maximum of 121°C for 15
minutes.

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14 Waste Disposal
Check Bacteria Filter
The bacterial/hydrophobic filter is an important device to help protect the pump
and environment from moisture and bacteria taken from patient airways.
Clements recommend that the filter be changed every month or when damp or
discoloured.
Change after every use when the unit is used on infectious patients.
After Every 100 Hours or 2 Months of Operation
• Check all suction tubing and replace if it is perished, soft or
discoloured. Also check the tubing connectors.
• Check the seal ring on the lid and replace if hard, cracked or
perished. Check the fit of the lid in the collection jar (canister).
• Check the overflow cut off valve seal and replace if perished or
damaged.
Waste Materials
The contents of the collection jars, suction tubing, bacteria filter,
internal exhaust filter may contain biohazardous wastes. Handle
using safe handling procedures, which may include the use of rubber
gloves and eye protection, and dispose of according to local protocols
for biohazardous materials.
Recycling
At the end of their service life, the pump and accessories should be
dismantled if necessary, and disposed of according to the WEEE
directive.

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15
Spare Parts
Spare Parts
SUC 81025 008 User Manual for SUC81030 Ceevac Suc ion Pump
SUC 81025 029 Pump, Mo or Uni , 240V 50Hz, ACeevac, Pis on
SUC 81025 034 Swi ch, ON/OFF for ACeevac
SUC 81030 001 Ki , 1L Reusable Collec ion Jar (Pack 1)
SUC 81030 005 Suppor Jar for FLOVAC Disposable 1L Liner
SUC 81030 007 Suppor Jar for FLOVAC Disposable 2L Liner
SUC 81030 009 Ki , Seal, Lid, 1L / 2L Reusable Jar (Pack 2)
SUC 81030 010 Ki , Lid Assembly for 1L / 2L Reusable Jar
SUC 81030 012 Ki , Fil er Bac eria/Hydrophobic (Pack 10)
SUC 81030 013 Ki , Silicone Tubing Se , Joiner (Pack 1)
SUC 81030 018 Ki , Vacuum Con rol for Ceevac/ACeevac
SUC 81030 020 Gauge, Vacuum 0 o -100 kPa for Ceevac/ACeevac
SUC 81030 042 Ki , 2L Reusable Collec ion Jar (Pack 1)
SUC 81030 121 Ki , 1L FLOVAC Disposable Liner (Pack 50)
SUC 81030 122 Ki , 2L FLOVAC Disposable Liner (Pack 50)
SUC 81030 132 Suppor Jar for FLOVAC Disposable 2L Liner
SUC 84500 033 Nipple, Yellow for FLOVAC Disposable Liner

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16
Troubleshooting
1. The Pump Fails To Operate
• Check that the mains power supply lead is firmly connected
and that the power is on at the mains power supply outlet.
• Check fuse as detailed below.
• Ensure that the Vacuum Gauge on the Control Panel indicates
zero. f not, release vacuum and switch pump off and on.
2. Pump Running But No Vacuum
• Check that all fittings are connected tightly.
• Turn the vacuum controller knob on the control panel and
watch the indicator on the vacuum gauge.
• Ensure that the silicone medical suction tubing is in good
condition and not old or cracked.
• Check the type of handpiece in use as some handpieces
require finger occlusion or trigger release to allow suction.
• Check bacteria/hydrophobic filter.
f the pump fails to work and you are unsure why, contact your
service department or return unit to your distributor.
Fuse Replacement
The ACeevac is fitted with a fuse located in a fuse holder that is
externally accessible
1. Disconnect the pump from the mains power supply.
2. Locate the fuse holder which is mounted on the rear side of
the unit at the lower right-hand side.
3. Pull out the fuse holder.
4. Remove the old fuse and inspect. f blown, replace it with a
new fuse of the same rating.
5. Replace the fuse holder cover.
Troubleshooting

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Wiring Diagram
Wiring Diagram

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18
Setup for Diagnostic and Performance Testing
Note that the following arrangements are not used for actual
suctioning applications. They are specified to remove
unnecessary variations when diagnosing faults and as a
standard setup for performance measurement.
Vacuum Check
Max
Vacuum
Gauge
Switch on pump and occlude inlet. Note maximum vacuum
reading.
Disconnect all items from inlet and with pump switched off,
confirm that gauge reads zero. A non-zero reading indicates a
faulty gauge.
Set vacuum control knob to maximum, switch on pump and
confirm that gauge reads zero. A non-zero reading indicates
obstruction in internal tubing or connections.
2.
Connect a calibrated vacuum gauge directly to inlet and repeat
maximum vacuum reading.
Confirm that pump gauge reads within the specified tolerance.
2. Occluded - vacuum check
Max
Vacuum
Gauge
3. Occluded - gauge check
Max
Vacuum
Gauge
Calibra ed
Vacuum
Gauge
1. Unoccluded - zero check
Diagnostic Setup

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Connect pump as shown in diagram. Set vacuum control knob
to maximum, and switch on pump. Occlude jar inlet and
confirm that pump achieves the same maximum vacuum as in
the previous vacuum check setup . Any difference indicates
leaks in jar or connections.
1. Occluded - leak check
Flow Check
Max
Vacuum
Gauge
Connect pump as shown in diagram. Set vacuum control knob
to maximum, and switch on pump. Connect jar inlet to
calibrated flow meter and note flow reading.
f flow is significantly below specification, check internal tubing
and pump itself (or internal shutoff valve if fitted).
2. Unoccluded - flow check
Max
Vacuum
Gauge
Collec ion
Jar
Calibra ed
Flowme er
Diagnostic Setup

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20 Periodic Safety Check
Periodic Safety Check
he following safety checks should be performed at least every 12
months by a qualified person who has adequate training, knowledge,
and practical experience to perform these tests.
* Inspect the equipment and accessories for mechanical and functional
damage.
* Inspect the relevant safety labels for legibility.
* Verify that the device functions properly as described in the
instructions for use.
* Perform electrical safety check.
Equipment Return for Repair
Before returning the ACeevac for repair, the external
surfaces and any accessories must be carefully
disinfected with a cloth soaked in methylated spirits or
hypochlorite-based solution. The pump and any
accessories should then be placed in a bag with a note
outlining the disinfection undertaken. Failure to follow
this procedure will result in the pump being returned
unrepaired. Equipment returned for repair must be
accompanied by a description of the problem. Unless
specifically requested, return the pump and power cable
only, excluding accessories such as jar, filter and tubing.
IMPORTANT
There are no user serviceable components inside.
Maintenance must be carried out by qualified
personnel only.