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240V Electric Suction Unit with 240V Electric Suction Unit with
Castors and Handle (Single Jar) Castors and Handle (Twin Jar)
INSPECTION
Remove the Electric Suction Unit from the packaging and inspect for damage. If there is any damage,
DO NOT USE, and contact Therapy Equipment Ltd.
FUNCTION/INTENDED USE
The Electric Suction Unit should only be used by Hospital personnel authorised and
trained in its use.
Read all instructions before using – DO NOT USE the Electric Suction Unit if you do
not understand the instructions given in these User Instructions.
The Function of the Electric Suction Unit is to provide a controlled Suction Source, which will
generate in excess of –575 mmHG (-75 kPa) by means of an Electric Motor. This is to enable suction
to be applied to the patient.
The unit is intended for use within a healthcare facility or domicilliary use, and is not considered
suitable for field (outside) or for transport use, or for high flow Theatre applications
USER INSTRUCTIONS
1. Ensure that the Mains Lead is fitted with a 3 pin fused 3 amp plug.
2. Connect the Mains/Plug into the Electric 240V Wall Socket and switch on the power.
3. Ensure the Hydrophobic Filter, clear Plastic Tubing, and all other connections are secure,
and not contaminated (If contaminated – change).
4. Ensure that the Receiver Jar is complete and functional.
5. Ensure that the Receiver Jar Liner (if fitted), is secure and correctly positioned within the
Receiver Jar.
6. Switch the Suction Unit on by pushing the Green Covered Switch located on the front panel
of the unit.
7. To pre-set the vacuum level before use, occlude the clear plastic tubing between the
Hydrophobic Filter and the Receiver Jar. Turn the Suction Controller – positioned on the top
of the unit – in an anti-clockwise direction. Read the suction level required on the Yellow
Vacuum Gauge positioned on the front panel of the unit. The Suction Unit is now ready for
use.
Should the operator wish to change the vacuum level during actual use. Turn the Suction Controller
to the new setting and read the vacuum level on the Yellow Gauge as previously described in No. 7
above.
The gauge is accurate to +/- 10%.
EXPLANATION OF LABEL
Indicates that the patient is isolated from Electric Earth with regards to this
equipment. The equipment is not suitable for direct cardiac.
Degree of protection against Electric Shock – Type BF applied Part
Type of Protection against Electric Shock – Class 1
ELECTROMAGNETIC COMPATIBILITY
The Therapy Equipment Disposable Suction Jar Liner can ONLY be used with the Therapy
Equipment Receiver Jar. Each Disposable Liner is individually packed with the full fitting
instructions on each pack.
The Suction Unit is fitted with a Hydrophobic Filter Unit. This is placed between the Patient
Receiver Jar and the Suction Pump Motor. This prevents liquids or solids from being inadvertently
sucked up into the Suction Pump Motor.
Should the filter come into contact with effluent, the filter will automatically shout down the Suction.
To replace the filter, detach clear hose, and pull upwards out of the unit. Push new filter into cavity
on top of the Suction Unit ensuring that the silicone grommet is in place, and re-connect clear hose.
It is not possible for the filter to come out during use, as the vacuum holds it in place.
IMPORTANT
Note: If the Filter or clear plastic tubing is contaminated i.e. discoloured stained or black, they
must be replaced and disposed of in the proper manner.
The tubing is considered disposable, and should not be cleaned and re-used. The tubing used is
clear PVC with a 7mm Bore (Part No. 4302).
The Electric Suction Unit is fitted with a 1.8 L Capacity Receiver Jar and Lid Assembly.
The Lid Assembly incorporates an Overflow Cut Off Float Assembly and Anti-Splash Tube. The
Receiver Jar is manufactured in Polysulphone.
When the Jar is full the hose should be disconnected and it should be lifted from the V Socket, in
the appropriate disposable area. The Jar Lid should be removed by pulling the Jar handle in the
opposite direction to the Lid handle and the contents emptied.
IMPORTANT
The Receiver Jar - Lid - Cut off Float Unit should not be autoclave as one assembly. Separate the
Unit into individual parts for autoclaving at up to 160°C
The component parts should be sterilised for a duration appropriate to the instructions on the
sterilisation device being used.
The Jar has a device within the jar to prevent overfill, and should always be used in a level plane.
This operates with a float sealing against a silicone filter. The Suction will stop when the overfill
device is activated and will re-start when the Jar is emptied. The usable capacity of the Jar is 1.8L.
A blue silicone Splatter Tube is fitted to the inside of the Lid, to minimise frothing. When re-
assembling after autoclaving, care should be taken to ensure that the orifice in the Splatter
Tube faces the outside of the Jar.
WARNINGS
DO NOT attempt to use if the collection canister is full, or if the Pipeline Protector is
wet or discoloured
TROUBLESHOOTING
The standard Electric Suction unit has not been manufactured using any Animal Tissue or
Phthalates. We should confirm however that Phthalates are used in the manufacture of the Suction
Tubing and Disposable Liner (full details are available on request).
HYDROPHOBIC FILTERS
Hydrophobic Filters Part No. 4902 Pack of 10
(For Electric Suction Unit)
RECEIVER JARS
DISPOSABLE LINERS
Circuit diagram, component lists, descriptions, calibration instructions and other information that will
assist the users are available to appropriately qualified technical personnel to repair and maintain
the equipment to the Standard designated by the manufacturer.
The pressure to which the product could be exposed should not exceed 1 Bar.
PREVENTATIVE MAINTENANCE
Each time the unit is used, a check should be made to ensure that full suction can be achieved.
This is effected by occluding the patient outlet on the Receiver Jar, switching the unit on to
Maximum Suction, and ensuring the Suction measures in excess of –575mmHG (-75kPa). In
addition, it is recommended that each unit be checked for function on an annual basis.
1) Remove old Pipeline Protector (Hydrophobic Filter) by detaching tubing and pulling the filter out
of its grommet. Dispose of old Pipeline Protector.
2) Fit new Pipeline Protector by pushing thread first into blue grommet (Do not re-attach suction
tubing until tests are complete).
3) Connect the Mains Lead (4201-44) into the chassis plug and connect to the mains
5) Occlude the Pipeline Protector outlet and turn the Suction Knob to MAXIMUM
6) Ensure the gauge on the Suction Unit reads approximately –575mmHG (-75kPa) within 6
seconds.
7) Connect the Electric Suction Unit to a 1.8Ltr and occlude the patient outlet. If fully functional the
Suction Controller should read -400mmHG within 6 seconds. This proves that the flowrates of
the unit are acceptable
8) Remove occlusion from Pipeline Protector (while Control Knob registering maximum), and
ensure that the gauge reading falls to register between 0 and –10kPa at free flow.
9) Re-occlude Pipeline Protector, and ensure the unit allows fully controllable suction levels over
the entire range by increasing and decreasing the Vacuum levels on the Control Knob.
10) Turn the Green Switch OFF and check the gauge registers Zero
11) Check the correct labels are being used on the Control Knob, and Top Cap, to indicate the level
of Suction i.e. Red Label, and Red Printing
Electric Suction User Instructions
Version G; January 2014
Page 6 of 6
It is not possible with correct operation to contaminate the motor. If, however, due to incorrect use
effluent has been drawn into the motor (vacuum pump), then the unit should be sealed within an
airtight heavy-duty plastic bag, and returned to the manufacturer.
The unit should be externally cleaned, by wiping the surface with an alcohol or disinfecting wipe.
The used wipes should be safely disposed of after use. If you suspect that the unit is contaminated,
remove it from use, and refer the device to the appropriate department. We do not recommend the
use of Detergent Based Hard Surface Wipes.
Revision No. 0 1 2 3 4 5 6
Date 06/01/99 01/10/03 26/11/09 25/10/12 01/02/13 24/06/13 15/01/14
Issue A B C D E F G