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ELECTRIC SUCTION UNIT - MEDICAL SUCTION HIGH VACUUM/HIGH

FLOW

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.

High Suction - Vacuum –100mmHG to at least –575 mmHG (-75 kPa) ;


Flowrate 24LPM (Adjustable levels –15kPa to –80kPa)
Technical Specification - 230V 50Hz 0.45 amp Fuse F 5A H 250V

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

• Not protected against the ingress of water - IPXO


• Equipment not suitable for use in the presence of a flammable anaesthetic mixture with air, or with
Nitrous Oxide.
Electric Suction User Instructions
Version G; January 2014
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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.

CHANGING THE VACUUM LEVEL DURING 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 unit complies with European Electromagnetic compatibility requirements.


It may emit electromagnetic radiation, which may interfere with other equipment in the close vicinity.
To minimise, maintain a reasonable distance between equipment.

DISPOSABLE JAR LINERS (Part No. 4807)

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.

HYDROPHOBIC FILTER (Part No. 4902)

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.

THIS FILTER MUST BE FITTED AT ALL TIMES


Electric Suction User Instructions
Version G; January 2014
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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

Before use: Check that the Hydrophobic Filter is clean


Check that the Hydrophobic Filter is correctly fitted

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).

RECEIVER JAR ASSEMBLY (Part No. 4800)

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 autoclave, or immerse in liquid

DO NOT attempt to use if the collection canister is full, or if the Pipeline Protector is
wet or discoloured

DO NOT use if the Electric Suction Unit becomes internally contaminated.

ENSURE all connections are tight and leak free


Electric Suction User Instructions
Version G; January 2014
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TROUBLESHOOTING

PROBLEM ANALYSIS ACTION


Cable becomes Electric Suction will not • Refer to manufacturer
Disconnected or Damaged function, or will revert to Battery
if dual function
Motor Failure Electric Suction will not • Refer to manufacturer
Function
Gauge not operational Pump would be operational, but • Refer to manufacturer
the gauge would not be
indicating the correct vacuum
Controller Mal-Function Cannot adjust the Suction • Refer to manufacturer
output of the Electric Suction
Unit
Disposal of waste products Spillage of effluent • Wear protective clothing
from Suction Jar • Refer to Hospital
management and
Infection Control
Authorities
Disposal of Equipment Infection Exposure • Ensure all appropriate
action is taken to prevent
exposure to parts of the
equipment
Final disposal of equipment • Contact manufacturer for
instructions

USE OF ANIMAL TISSUES/PHTHALATES

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).

REPLACEMENT PARTS DETAILS

HYDROPHOBIC FILTERS
Hydrophobic Filters Part No. 4902 Pack of 10
(For Electric Suction Unit)

RECEIVER JARS

Complete Assembly Part No. 4800

DISPOSABLE LINERS

Disposable Liners (1.8 L capacity) Part No. 4807 Box of 50

PLASTIC SUCTION TUBING

Plastic Suction Tubing Part No. 4302 30M coil


Electric Suction User Instructions
Version G; January 2014
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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.

TRANSPORT AND STORAGE

The product should be stored in a clean dry environment.


The Storage temperature should be within the range -25°C to +50°C.

The humidity should not exceed 95%.

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.

Annual Function Testing

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

4) Turn the Suction Unit ON by pressing the Green Switch

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
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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.

A FULL SPARES AND REPAIR SERVICE IS AVAILABLE ON ALL PRODUCTS

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

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