Anetic Aid QA4 User manual

Contents Page
Document No. 992010. Issue 15 –12.01.21
Introduction
1. Introduction . . . . . . . . 1
1.1. Warnings and Cautions . . . . . . 1
1.2. Intended Use and Contraindications . . . . . 1
1.3. Equipment Classification . . . . . . 1
1.4. Serial Number Label . . . . . . . 1
1.5. Putting Trolley into Service . . . . . . 1
1.6. Abridged Summary of Warnings and Cautions . . . 2
Product Specifications
2. Product Specifications . . . . . . . 4
Product Functions
3. Product Functions . . . . . . . . 6
4. Introduction to Powered Functions . . . . . 7
5. Using the Handset . . . . . . . . 7
6. Using the Height Adjustment . . . . . . 8
7. Using the Backrest . . . . . . . . 8
8. Selecting the Lateral Tilt or Patient Platform Traverse Function . . 8
9. Using the Lateral Tilt . . . . . . . 8
10. Using the Patient Platform Traverse (‘C’ Arm Access) . . . 8
11. Using the Trendelenburg Function . . . . . . 9
12. Introduction to Manual Functions . . . . . . 10
13. Using the Brakes . . . . . . . . 10
14. Using the Steering Pedal, activates 5th wheel . . . . 10
15. Using the Head Section . . . . . . . 10
16. Using the Leg Section . . . . . . . 10
17. Using the Single Piece Siderail . . . . . . 12
18. Using the Emergency Backrest Release Function . . . . 13
19. Using the Transfusion Pole . . . . . . . 13
General Product Information
20. Battery Charging and Maintenance . . . . . 15
21. Patient Weight Limits . . . . . . . 16
22. K8 Pressure Care Mattress . . . . . . . 16
23. Cleaning and Disinfecting the Trolley . . . . . 17
24. Product Warranty . . . . . . . . 17
25. Product Maintenance . . . . . . . 18
26. Label Identification . . . . . . . 18
Product Accessories
27. Product Accessories . . . . . . . 22
28. Using the Articulating Leg Section (catalogue no. 21355) . . . 23
29. Using the Dual-articulating Head Positioner (catalogue no. 22325) . 23
30. Using the Urology, Retrograde Pyelography, Gynaecology Extension . 24

Introduction
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1. Introduction
These instructions are intended to assist you with the operation of the QA4™ Powered
Mobile Surgery System. It is important that these instructions are read thoroughly
before using the equipment.
It is also important to check the trolley before use to ensure there is no loss or change in
performance; ensure that all trolley functions operate to their full range of movement
and that all components disengage, re-engage and lock correctly. We recommend that
the trolley is visually inspected for any loose or damaged parts, and foreign bodies
caught in the castors.
NOTE:
If the trolley is damaged or faulty it must be taken out of use with
immediate effect and the fault reported to Anetic Aid, your authorised
dealer or maintenance department. The trolley must not be used until the
damage or fault has been repaired.
1.1. Warnings and Cautions
Various warnings and cautions are made throughout these operating instructions.
A WARNING is given when the personal safety of the patient or user may be
affected and when disregarding this information could result in injury.
A CAUTION is given when special instructions must be followed.
Disregarding this information could result in permanent damage being
caused to the trolley.
1.2. Intended Use and Contraindications
This product is intended for use within a clinical environment for the induction,
transport, treatment and recovery of patients.
CONTRAINDICATIONS:
The trolley is not compatible with hospital bed/trolley washers.
The trolley must not be used near magnetic resonance imaging (MRI) machines, or
any machines generating a large magnetic field.
Do not use the trolley for transporting patients in a moving vehicle.
The trolley has very low ground clearance beneath the central column that may cause
problems when traversing uneven ground and inclines.
The trolley should not be used outside; it may be damaged by pushing it across rough
or uneven ground.
1.3. Equipment Classification
The equipment referenced in this document is CE marked and has been classified as a
Class 1 Medical Device under the scope of both the Medical Devices Directive 93/42/EEC
and the Medical Device Regulation 2017/745.
1.4. Serial Number Label
The serial number label is located on the cover moulding beneath the patient platform.
1.5. Putting the Trolley into Service
Care should be taken when removing the packaging, avoid the use of sharp implements
wherever possible.
It is important that the trolley is working properly, fully charged, cleaned and
disinfected before it is put into service. Use this manual to check all the functions and
refer to Section 20, ‘Battery Charging and Maintenance’, and Section 23, ‘Cleaning and
Disinfecting the Trolley’.

Introduction
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The trolley should only be used, for its intended use, by suitably trained personnel who
have familiarised themselves with the functions of the trolley. Our representatives are
available for on-site consultation or training and our head office team will be pleased to
answer any queries you may have.
1.6. Abridged Summary of Warnings and Cautions
In common with all medical devices of this nature there are inherent risks that the user
should be made aware of, including potential pinch points from moving parts. Whilst
every effort has been taken to eliminate these risks, care should be taken when using
the trolley. It is important that the user familiarise themselves with all of the warnings
and cautions contained within this document.
CAUTIONS:
The battery must be properly maintained in accordance with these
instructions. Failure to do so will result in significant loss of charge capacity
or failure of the battery. Refer to Section 20, ‘Battery Charging and
Maintenance’ for a full explanation on how to care for the battery.
Ensure that there are no obstructions in the way before raising or lowering
the backrest.
Ensure that there are no obstructions in the way before traversing the
patient platform.
With the articulating leg section articulated downwards, the patient
platform cannot be traversed towards the head end passed the neutral
position.
Ensure that there are no obstructions in the way before tilting the patient
platform.
Ensure that there is no equipment stored in the base moulding of the
trolley before tilting the patient platform. NOTE: This ONLY applies when
the trolley is at its lowest height.
Applying the steering pedal with excessive force, i.e. by standing on it, may
cause permanent damage to the mechanism.
The siderail should be returned to the mid-section of the trolley during
patient recovery.
Failure to charge the battery once the low battery alarm has sounded could
result in a permanent loss of maximum charge capacity.
Only batteries supplied and approved by Anetic Aid should be used.
The battery unit should not be opened.
Use the battery only for its intended purpose.
Never use a battery that is damaged.
The battery must be recycled, properly disposed of or returned to Anetic
Aid. The battery must not be discarded with Household waste.
Ensure that the mattress is correctly orientated on the patient platform with
the touch fastener of the mattress aligning with the touch fastener on the
patient platform.
Ensure that the mattress is centrally positioned across the width of the
patient platform otherwise it may prevent the side rail from locking when
raised.
Do not steam clean, jet wash, soak or immerse this device.
Do not use concentrated bleaching disinfectant solutions, organic solvent or
abrasive powders in the cleaning or disinfection of this product.
Dilute all disinfectants in accordance with the manufacturer’s guidelines.
Disinfectant products are corrosive in nature; failure to properly wash and
dry the product surface could leave a corrosive residue which may cause
damage to the product. Ensure the mattress is thoroughly dried before
refitting.
In line with the MHRA document, Managing Medical Devices, maintenance
work should only be conducted by suitably trained personnel following
manufacturer’s guidelines.

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WARNINGS:
Ensure there is nothing to impede the raising or lowering of the patient
platform as this could result in damage to the equipment and/or injury to
the patient.
When leaving patients unattended the trolley should be fully lowered to
minimise any risk of injury should the patient fall off the trolley.
Always apply the brakes when leaving a patient unattended, a patient is
getting on or off the trolley, or transferring patients from the trolley to
another platform.
When the head section is fitted on to the trolley, ensure that the head
section is fully engaged and securely locked in position.
Ensure that the leg section is fully engaged and securely locked in position.
Ensure that any persons responsible for removing the leg section adopt
good posture and stance, in accordance with the relevant ‘Moving and
Handling’ policies, to prevent injury to the user.
Failure to secure the siderail to the side bar using the locking clamp could
result in injury to the patient.
Caution is required when releasing the emergency backrest handle. Once
the handle is released, the backrest will drop with limited resistance.
Therefore, ensure no persons are stood behind or under the backrest when
the handle is released.
Ensure that the handle is properly re-engaged. Failure to do so will result in
the backrest not functioning correctly and possibly disengaging
unexpectedly.
Only use the lead supplied with the trolley for charging purposes. Do not
use the lead for any other purposes.
Visually inspect the lead for damage on a daily basis. Do not use the lead if
damaged in any way.
Exceeding any of the maximum specified weight limits could result in failure
of the trolley and injury to the patient and staff.
Incompatible mattresses can create hazards; only replace the mattress with
a new mattress supplied by Anetic Aid, or your authorised dealer, to ensure
compatibility in accordance with BS EN 60601-2-52:2010.

Product Specifications
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2. Product Specifications
Key to Fig. 1:
Trolley Dimensions and Weight:
A
Minimum trolley height
605mm (24.0”)
Maximum trolley height
1005mm (39.5”)
NOTE: Height is measured from the floor to the patient platform and does not include
the mattress.
B
Trolley length
2100mm (82.7”)
C
Trolley width to the outside of the side bar
655mm (25.8”)
D
Trolley width to the outside of the siderails
770mm (30.3”)
E
Brake width with brakes off
800mm (31.5”)
F
Base length
1190mm (47.0”)
G
Base length including 5th wheel
1330mm (52.0”)
Castor Diameter
150mm (6.0”)
Trolley Weight
160kg (330lb)
Mattress Dimensions:
H
Mattress length
2040mm (80.0”)
I
Mattress width
600mm (23.6”)
Mattress depth
75mm (3.0”)
NOTE: Refer to Section 22, ‘K8 Pressure Care Mattress’, for full specification details.
Trendelenburg and Lateral Tilt Range of Movement:
Trendelenburg
20°
Reverse Trendelenburg
12°
Lateral Tilt
±12°
Backrest and Head Section Range of Movement:
Backrest Articulation
0 - 65°
Head Section Articulation
+25/-30°
NOTE: The backrest actuator is designed to lift a maximum of 45% of the 250kg (550lb)
patient weight limit; this equates to 112.5kg (248lbs). If the weight on the backrest exceeds
this figure, then the backrest actuator may stall, and the backrest will not raise. This can be
caused by exceeding the patient weight limit, or having the patient positioned too far up the
backrest towards the head end.

Product Specifications
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C-Arm Traverse Range of Movement:
Head End Traverse
230mm (9.0”)
Foot End Traverse
230mm (9.0”)
Patient Weight Limits:
Trolley
250kg (550lb)
Head Section
25kg (55lb)
Leg Section
50kg (110lb)
Safe Working Load (SWL)
300kg (660lb)
NOTE: The trolley can be used in all positions with the maximum patient weight specified.
Standard Lightweight Leg Section:
Weight
6kg (13lb)
Articulation range
N/A
Articulating Leg Section (optional):
Weight
11kg (24lb)
Articulation range
0 –45°
Electrical Specification:
Mains charging input (dependant on control box option)
230VAC, 50Hz, 1.3A
100VAC ± 10%, 50/60Hz, 2.5A
Battery specification
2 x lead acid cells, 24V, 4.5Ah
Standard mains lead
(This is the standard lead supplied, unless otherwise
specified at the time of ordering)
3m IEC C13 Socket to UK Plug,
Fused 5A
Full charge time from flat
8 hrs
NOTE: The charging figures quoted are dependent upon the age and condition of the
battery, and are guidelines only.
Electrical Classification:
The electrical classification for this product is; Class II Type B, fitted with a Functional Earth.
NOTE: The trolley is fitted with a functional earth connecting the mains inlet socket to the
base frame. Electrical Safety Enclosure Leakage tests will be inaccurate due to the functional
earth. The functional earth should be detached before performing Enclosure Leakage tests.
CAUTION: Ensure that the functional earth is reattached after testing.
EMC Compatibility:
Electromagnetic Compatibility: product conforms to IEC 60601-1-2:2014
Environmental Conditions:
Temperature:
Operation
10°C to 50°C
Storage & Transport
-20°C to 50°C
Relative Humidity:
Operation
30% to 75%
Storage & Transport
10% to 75%
Atmospheric Pressure:
Operation
70kPa to 106kPa
Storage & Transport
50kPa to 106kPa
Environmental Regulatory Information; WEEE, waste batteries, etc.
For the latest information about Anetic Aid’s environmental policy, WEEE policy, and the safe
disposal of this product, please refer to our website.
NOTE: All dimensions quoted are subject to the following tolerances; angles ±5°, lengths and
widths ±25mm (±1”), depths ±10mm (±0.4”). Anetic Aid reserves the right to change
specifications without notice.

Product Functions
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3. Product Functions
Key to Fig. 2
1.
Handset
2.
Brake Pedals
3.
Steering Pedal
4.
Lateral Tilt / Patient Platform Traverse Switch
5.
Head Section Tilt Actuation Lever
6.
Leg Section Articulating with 105mm Sidebar (optional)
7.
Single Piece Siderail
8.
Pushing Handles
9.
Oxygen Cylinder Mounting Recess
10.
‘V’ Mounting for Suction Canister
11.
Mains Input/Charging Socket
12.
Handset Socket
13.
Transfusion Pole

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4. Introduction to Powered Functions
This section of the document gives a description of product functions that are
electromechanical powered, either from the trolleys internal battery supply, or when
the trolley is connected to the mains power supply (using the power lead supplied).
These functions are operated and controlled from the handset (item 1, fig. 2).
CAUTION: The battery must be properly maintained in accordance with these
instructions. Failure to do so will result in significant loss of charge capacity or
failure of the battery. Refer to Section 20, ‘Battery Charging and Maintenance’
for a full explanation on how to care for the battery.
5. Using the Handset
The handset connects into the handset socket on the base of the trolley at the head end
(item 12, fig. 2). The handset button functions are detailed below.
NOTE:
The manufacturer recommends that a spare handset is purchased and stored
in an accessible location, in the event that the handset becomes damaged.
Key to Fig. 3
1.
Battery Status LED
2.
Variable Height Function
3.
Backrest Articulation Function
4.
Lateral Tilt and Patient Platform Traverse Function (shared button operation)
5.
Trendelenburg & Reverse Trendelenburg Tilt Function

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CAUTION: The handset is in constant use, so it is particularly vulnerable to
wear and tear or damage. Before use it is important to inspect the handset to
ensure there is no damage to the cable or the buttons.
WARNING: In the event of handset damage the handset should be replaced
immediately or the trolley removed from service.
WARNING: Handset damage may lead to malfunction during equipment use.
If a handset button becomes damaged it is possible for one of the powered
functions to operate spontaneously. In this unlikely event, the following
actions should be taken;
1. Depress and hold the opposing function button, i.e. if the backrest is
raising press backrest down.
2. Unplug the handset from the trolley.
3. Fit a new handset.
4. If another handset is not available transfer the patient to another trolley.
6. Using the Height Adjustment
The height of the patient platform can be adjusted using the up and down buttons on
the handset.
WARNING: Ensure there is nothing to impede the raising or lowering of the
patient platform as this could result in damage to the equipment and/or injury
to the patient.
WARNING: When leaving patients unattended the trolley should be fully
lowered to minimise any risk of injury should the patient fall off the trolley.
7. Using the Backrest
The backrest can be raised and lowered using the up and down buttons on the handset.
NOTE:
The backrest actuator is designed to lift a maximum of 45% of the 250kg
(550lb) patient weight limit; this equates to 112.5kg (248lbs). If the weight on
the backrest exceeds this figure, then the backrest actuator may stall, and the
backrest will not raise. This can be caused by exceeding the patient weight
limit, or having the patient positioned too far up the backrest towards the
head end.
CAUTION: Ensure that there are no obstructions in the way before raising or
lowering the backrest.
8. Selecting the Lateral Tilt or Patient Platform Traverse Function
To use either the lateral tilt, or the patient platform traverse, the rocker switch must be
set to the required function. The rocker switch is located on the patient right hand side
of the mid-section (item 4, fig. 2).
9. Using the Lateral Tilt
Firstly, select the function using the rocker switch. The patient platform can now be
laterally tilted (along the longitudinal axis) to the patients’ left hand side, or the
patients’ right hand side, using the left and right buttons on the handset.

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10. Using the Patient Platform Traverse
The patient platform is designed to traverse longitudinally, towards both the head end
and the foot end. The traverse function enables full ‘C’ arm coverage, and improved
surgical access from both the head end and foot end.
Firstly, select the function using the rocker switch; the patient platform can now be
traversed using the left and right buttons on the handset.
The mattress and patient platform are made from x-ray translucent materials. The areas
of ‘C’ arm access are illustrated in fig. 5, with the trolley traversed in both directions.
Observe that when the patient platform is traversed in either direction, the mid-section
static frame arm is revealed. In the neutral position the traversing section of the patient
platform aligns with the static arm. The trolley should be returned to the ‘neutral’
position once the procedure has been completed.
NOTE:
The patient platform should be returned to the neutral position once the
procedure has been completed, see above.
CAUTION: Ensure that there are no obstructions in the way before traversing
the patient platform.
CAUTION: With the articulating leg section articulated downwards, the
patient platform cannot be traversed towards the head end passed the
neutral position.

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11. Using the Trendelenburg Function
The patient platform can be longitudinally tilted to provide a Trendelenburg (head
down) or reverse Trendelenburg (leg down) position by using one of the two down
buttons on the handset. The head down Trendelenburg button is in-filled in red to
indicate that this button is used for emergency positioning.
CAUTION: Ensure that there are no obstructions in the way before tilting the
patient platform.
CAUTION: Ensure that there is no equipment stored in the base moulding of
the trolley before tilting the patient platform. NOTE: This ONLY applies when
the trolley is at its lowest height.
12. Introduction to Manual Functions
This section of the document gives a description of product functions that are manually
operated, and how to use them.
13. Using the Brakes
All four castors are simultaneously braked by depressing either of the brake pedals at
any point along the length of the pedal (item 2, fig. 2). The brakes are disengaged by
lifting either pedal.
WARNING: Always apply the brakes when leaving a patient unattended, a
patient is getting on or off the trolley, or transferring patients from the trolley
to another platform.
14. Using the Steering Pedal, activates 5th wheel
The trolley can be manoeuvred more easily by engaging the 5th wheel steering
mechanism (item 3, fig. 2). The mechanism is engaged, and disengaged, by pressing
down on the steering pedal. To move the trolley sideways disengage the 5th wheel.
CAUTION: Applying the steering pedal with excessive force, i.e. by standing on
it, may cause permanent damage to the mechanism.
15. Using the Head Section
The head section can be detached from the trolley to improve surgical/anaesthetic
access, and to allow other head section options to be fitted; see Section 27. ‘Product
Accessories’.
Removing the head section, prior to administering anaesthetic, reduces the length of
the backrest, and the need to reposition the patient in theatre. Removing the head
section also gives greater access to the patient from the head end for theatre staff.
The head section is articulated by pulling up on the head section tilt actuation lever
(item 5, fig. 2). To remove the head section, lift the release handle, then lower and
remove the head section from the support bracket; as illustrated in fig. 6 and fig. 7.
WARNING: When the head section is fitted on to the trolley, ensure that the
head section is fully engaged and securely locked in position.
16. Using the Leg Section
The trolley is fitted as standard with a non-articulating lightweight leg section. If the
trolley is fitted with an articulating leg section refer to Section 28.
To remove the leg section, depress each button in turn located one on each side of the
trolley, and remove the leg section; see fig. 8. To replace the leg section, align the
spigots of the leg section into the mating female sockets on the trolley, and push home
firmly until the leg section is fully engaged; see fig. 9.

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Product Functions
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WARNING: Ensure that the leg section is fully engaged and securely locked in
position.
WARNING: Ensure that any persons responsible for removing the leg section
adopt good posture and stance, in accordance with the relevant ‘Moving and
Handling’ policies, to prevent injury to the user.
17. Using the Single Piece Siderail
The trolley is supplied with two single piece siderails that attach directly onto the side
bar.
NOTE:
The siderails are intended to be located on the mid-section of the trolley for
two reasons;
Firstly, with the siderails on the mid-section the patient coverage is
adequate for both the upper and lower torso with the backrest either
horizontal or articulated; see fig 10.
Secondly, the backrest actuator is designed to lift the weight of the
backrest and 45% of the patient weight. Exceeding this weight may cause
the backrest actuator to stall, and the backrest will not raise. Locating the
siderails on the backrest increases the weight on the backrest, which
reduces the patient weight that can be lifted.
CAUTION: The siderail should be returned to the mid-section of the trolley
during patient recovery.
WARNING: Failure to secure the siderail to the side bar using the locking
clamp could result in injury to the patient.
To attach the siderail (fig. 11); holding the siderail vertically, pull up on the siderail
release handle (A); this will allow the locking clamp (B) to articulate. Holding the locking
lever (C), position the clamp (B) onto the siderail, and rotate the locking lever (C)
clockwise, or anticlockwise, to lock the siderail in position (fig. 12). Reverse this
technique to remove the siderail.
The siderail can be rotated down whilst still attached to the trolley. With the siderail still
secured to the trolley, pull up on the release handle (A) as indicated in fig. 13 and rotate
the cotside away from the trolley into the down position.
18. Using the Emergency Backrest Release Function
The emergency backrest release handle allows the backrest to be dropped immediately
from any articulated angle to the horizontal position.
NOTES:
When the emergency backrest release handle is disengaged the backrest will
not function; the backrest handle must be engaged for correct backrest
operation.
It is important that staff are clearly informed as to the location of the
emergency release handle, its function, and mode of operation.
To release, grasp the emergency release handle and rotate the handle anticlockwise. As
the handle is released the backrest will be unsupported and will drop to the horizontal
position; see fig. 14.
WARNING: Caution is required when releasing the emergency backrest
handle. Once the handle is released, the backrest will drop with limited
resistance. Therefore, ensure no persons are stood behind or under the
backrest when the handle is released.
Follow these steps to re-engage the release handle. With the backrest horizontal
depress the backrest down button, see fig. 3, to ensure that the backrest actuator is
retracted to its shortest length. Now grasp the emergency release handle and rotate the
handle 90 degrees clockwise until the handle ‘clicks’ into position and physically stops;

Product Functions
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see fig. 15. The release handle is now re-engaged enabling the backrest to be operated
from the handset.
WARNING: Ensure that the handle is properly re-engaged. Failure to do so
will result in the backrest not functioning correctly and possibly disengaging
unexpectedly.

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19. Using the Transfusion Pole
The trolley is fitted with a loose transfusion pole (item 13, fig. 2) that can be fitted at
any point along the side bar and secured using the locking lever.
To adjust the height of the transfusion pole, as illustrated in fig. 16. Grasp the locking
mechanism (A) and using your thumb, lift the mechanism to release the lock and move
the pole up or down to the required height (B); release the mechanism to lock the pole
in any position.
The transfusion pole is fitted with two spring-loaded hooks that are designed to return
to their original, upright position, when not in use. Swivel one or both hooks outwards
(C) to hang the IV bags.
NOTE:
The maximum weight limit per IV hook is 3kg (6.6lbs) or 3 litres (101.4 fl oz),
and the safe working load for the IV pole is 6kg (13.2lbs).

General Product Information
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20. Battery Charging and Maintenance
The battery will require recharging at regular intervals. The frequency with which the
battery requires recharging will be dependent on how often the equipment is used, and
the general condition of the battery.
NOTES:
The manufacturer recommends that the trolley is put on charge when not in
use, including overnight. Establishing this routine will ensure that the trolley
does not run out of charge in the course of a day.
If the trolley is going to be placed in storage the trolley must be charged for
8 hours every 2 weeks. Failure to do so will result in permanent battery
damage.
It is recommended that the battery is replaced every 3 years.
The trolley is supplied with an IEC mains power lead which is used to charge the on-
board battery (specification in ‘Electrical Specification’ on page 5). The power lead
should be plugged into a mains socket and the appliance connector end plugged into
the charging socket on the trolley (item 11, fig. 2). The socket should now be switched
on.
WARNING: Only use the lead supplied with the trolley for charging purposes.
Do not use the lead for any other purposes.
WARNING: Visually inspect the lead for damage on a daily basis. Do not use
the lead if damaged in any way.
Once the mains power lead is connected the control unit will check the charge capacity
of the battery before commencing charging, this may take up to 12 minutes. Once this
test is complete the battery will either; begin to charge and the battery status LED on
the handset will flash ‘green’, or the battery status LED will turn solid ‘green’ to indicate
that the battery is fully charged.
From flat, the battery will take approximately 8 hours to fully charge. Plugging the
trolley in for a short period of time will only partially recharge the battery.
The trolley can be left on charge permanently as there is no danger that the battery can
be over charged. The control unit manages the status of the battery charge, switching
the charging circuit off when the battery is full and back on when the charge dissipates
below a pre-set level.
When the battery charge is low the control unit will emit a continuous ‘beeping’ tone
when any one of the function buttons is being depressed, and the handset battery
status LED will turn ‘amber’. This indicates that the battery must be recharged; failure
to do so will result in the deep discharge protection being enabled.
CAUTION: Failure to charge the battery once the low battery alarm has
sounded could result in a permanent loss of maximum charge capacity.
If the battery has not been charged and the trolley is continuously used, the battery will
run flat and eventually reach a ‘deep discharge’ condition. A normal 8 hour charging
period will not be sufficient to recover the battery. The battery will need to be on
charge for approximately 72 hours to fully recover.
CAUTION:
Only batteries supplied and approved by Anetic Aid should be used.
The battery unit should not be opened.
Use the battery only for its intended purpose.
Never use a battery that is damaged.
The battery must be recycled, properly disposed of or returned to Anetic
Aid. The battery must not be discarded with Household waste.

General Product Information
Document No. 992010. Issue 15 –12.01.21
Page 16
21. Patient Weight Limits
The trolley is designed to accommodate a maximum patient weight of 250kg, and a safe
working load of 300kg (SWL). Patients should mount the trolley at the centre of the
patient platform and their weight kept as evenly distributed as possible whilst on the
trolley.
Note that all the removable head sections are designed to take a maximum weight of
25kg, and the removable leg section is designed to take a maximum weight of 50kg.
NOTE:
The safe working load (SWL) is the sum of the maximum patient weight, the
weight of any accessories attached to the trolley and the weight of the items
on or attached to those accessories.
WARNING: Exceeding any of the maximum specified weight limits could
result in failure of the trolley and injury to the patient and staff.
22. K8 Pressure Care Mattress
The mattress is fixed to the patient platform with touch fastener; this enables the
mattress to be removed from the trolley for cleaning and replacement.
NOTES:
When fitting a new mattress to the trolley the touch fastener on the patient
platform must also be replaced.
The mattress parts should be visually inspected for damage on a daily basis.
If the outer mattress fabric is torn, then fluids may penetrate and the
mattress should be replaced. Do not attempt to repair tears or splits with
self-adhesive tapes.
WARNING: Incompatible mattresses can create hazards; only replace the
mattress with a new mattress supplied by Anetic Aid, or your authorised
dealer, to ensure compatibility in accordance with BS EN 60601-2-52:2010.
CAUTION: Ensure that the mattress is correctly orientated on the patient
platform with the touch fastener of the mattress aligning with the touch
fastener on the patient platform.
CAUTION: Ensure that the mattress is centrally positioned across the width
of the patient platform otherwise it may prevent the side rail from locking
when raised.
K8 Pressure Care Mattress Specification
Latex free
X-ray translucent
Foam Base Layer
Polyether polyurethane foam, density 48 to 52kg/m², nominal
hardness 210N –250N
Foam Top Layer
Viscoelastic temperature sensitive foam, density 58 to 62kg/m²,
nominal hardness 70N –100N
Fabric Cover
Polyurethane coated nylon, polyamide, polyester which is; breathable,
anti-microbial, chlorine resistant (<1%, 10,000 ppm) and waterproof
(to 2000mm)
Touch Fastener
Polyamide with high strength adhesive
Fabric Cover Seams
High frequency welded seams which are fully sealed and high
strength
Fire Safety
Compliant to Fire Crib Test 5 BS7177
Life Expectancy
The mattress life expectancy is 4 years. Dependent upon the level of
care and maintenance the pressure care properties of this mattress
may reduce once the life expectancy has been exceeded
Warranty
The mattress is guaranteed against defects found in material or
workmanship for a period of 12 months from the date of invoice.
Judith Waterlow Score
The mattress is rated as medium to high risk and suitable for the
majority of patients up to 23 hours. It is important to remain aware of
individual patient needs, and standard nursing practices must always
apply for patients immobile or at high risk to pressure sores

General Product Information
Document No. 992010. Issue 15 –12.01.21
Page 17
23. Cleaning and Disinfecting the Trolley
It is recommended that only CE marked cleaning products are used in the cleaning of
the trolley and the mattress. Cleaning and disinfection should be carried out by hand
only.
CAUTION:
Do not steam clean or jet wash this device.
Do not soak or immerse this device.
Do not use concentrated bleaching disinfectant solutions, organic solvent
or abrasive powders in the cleaning or disinfection of this product.
Dilute all disinfectants in accordance with the manufacturer’s guidelines.
Disinfectant products are corrosive in nature; failure to properly wash and
dry the product surface could leave a corrosive residue which may cause
damage to the product. Ensure the mattress is thoroughly dried before
refitting.
Clean the trolley and mattress with warm water and neutral detergent and dry the
surfaces thoroughly using a soft cloth. Suitable disinfectants are: quaternary
ammonium compounds, isopropyl alcohol & chlorine bleach; refer to the table below.
Apply disinfectant by cloth, spray or disinfectant wipe. Following disinfection, wash off
all surfaces with clean warm water and dry thoroughly using a soft cloth. Clean all
touch fastener attachments periodically with a soft brush, neutral detergent and
suitable disinfectant as stated. The product will be adversely affected and its life
expectancy reduced if the above cautions are not observed.
Compound
% Active
pH Range
Dwell Time
Chlorine
<10,000ppm (1%)
7-9
≤10 mins.
Chlorine is suitable, ensure the surfaces are rinsed and thoroughly dried as instructed.
Alcohol
70 (typical)
N/A
≤10 mins
Alcohol is suitable, subject to the following precaution; the surfaces must be rinsed
and thoroughly dried as instructed (if not the PU coating may swell and be vulnerable
to damage).
Hydrogen Peroxide
3-25%
5-9
≤5 mins.
Hydrogen Peroxide is conditionally suitable; the compound must be fully neutralized,
and the surfaces must be rinsed and thoroughly dried as instructed. Highly alkaline
peroxide pH≥10 is not suitable.
Quaternary Ammonium
3-15%
7-13
Varies
Quaternary Ammonium is conditionally suitable; the surfaces must be rinsed and
thoroughly dried as instructed. Quaternary Ammonium’s are typically too alkaline,
those with a pH≥10 are not suitable. Do not use QUAT wipes containing sodium
hydroxide.
24. Product Warranty
The product, when new, is guaranteed to be free from defects in materials and
workmanship and to perform in accordance with the manufacturer’s specification for a
period of one year from the date of invoice from Anetic Aid or their approved
distributor. Anetic Aid will repair or replace, at their discretion, any components found
to be defective or at variance with the manufacturer’s specification within this time at
no cost to the purchaser.
Protect your investment with a manufacturer backed service and
maintenance package; contact Anetic Aid for more details.
Warranty exclusions; the warranty does not provide cover for breakage or failure due to
tampering, misuse, neglect, accidents, modifications or shipping. The warranty is also
void if the product is not used in accordance with the manufacturer’s instructions or is
repaired during the warranty period by any persons other than Anetic Aid or its
appointed agent. No other expressed or implied warranty is given.