Arjo MAA4020M User manual

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使用说明书 · Bedienungsanleitung · Mode d’emploi · Istruzioni per l’uso · Gebruiksaanwijzing
INSTRUCTIONS FOR USE
Paediatric Slings
04.SP.00-INT1_704.SP.00-INT1_7
••
11/202211/2022

2
WARNING
To avoid injury, always read this Instructions for Use and accompanied documents
before using the product. Mandatory to read the Instructions for Use.
Design Policy and Copyright
® and ™ are trademarks belonging to the Arjo group of companies.
© Arjo 2022.
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 Arjo.
Foreword
Thank you for purchasing Arjo equipment. Please read this Instructions For Use (IFU)
thoroughly!
Arjo will not be held responsible for any accidents, incidents or lack of performance that occur as a result of any
unauthorized modication to its products.
Customer Support
If you require further information, please contact your local Arjo representative. The contact information is
located at the end of this IFU.

WARNING Means: Safety warning. Failure to understand and obey this warning may result in injury
to you or to others.
CAUTION Means: Failure to follow these instructions may cause damage to all or parts of the
system or equipment.
NOTE Means: This is important information for the correct use of this system or equipment.
Contents
Foreword .............................................................2
Customer Support ...................................................2
Denitions in this IFU ..............................................2
Intended Use .......................................................3
Patient/Child Assessment .......................................3
Expected Service Life .............................................3
Safety Instructions...............................................4
Safety Practises ......................................................4
Serious incident.......................................................4
Parts Designation ................................................5
Preparations ........................................................5
Before First Use (6 steps) .......................................5
Before Every Use (6 steps) .....................................5
Select Sling Size..................................................6
Using the Arjo Measuring Tape
(4 steps) (Accessory) ..............................................6
Sizing Without a Measuring Tape (2 steps).............6
Sling Selection.....................................................6
Allowed Combinations.........................................7
Safe Working Load (SWL).......................................7
Clip Attachment & Detachment............................7
Attach the Clips (5 steps) ........................................7
Detach the Clips (3 steps).......................................7
Applying the Sling................................................8
In Bed (22 steps).....................................................8
In Chair/ Wheelchair (17 steps)...............................8
On Floor (31 steps) .................................................9
Removing the Sling ...........................................11
In Bed (12 steps)................................................... 11
In Chair/Wheelchair (13 steps).............................. 11
Cleaning and Disinfection..................................12
Cleaning Instruction (5 steps) ...............................12
Cleaning Chemicals ..............................................12
Disinfection............................................................12
Care and Preventive Maintenance ....................12
Before and After Every Use...................................12
When Soiled or Stained and Between Patients ....12
Storage..................................................................12
Service and Maintenance......................................12
Troubleshooting.................................................13
Technical Specications ....................................14
Label on the Sling..............................................15

ENEN

3
Intended Use
The Paediatric clip sling is a product intended for
assisted transfer of Paediatric patient/child with limited
ability to move and require full body support during
transfers.
The Paediatric clip sling shall only be used by
appropriately trained caregivers with adequate
knowledge of the care environment, and in accordance
with the instructions outlined in the Instructions for
Use.
Paediatric clip sling is intended for children.
The Paediatric clip sling is intended to be used in
hospital environments, nursing homes, other healthcare
facilities and home care.
The Paediatric clip sling should only be used for the
purpose specied in this Instructions for Use. Any
other use is prohibited.
Patient/Child Assessment
We recommend that facilities establish regular
assessment routines. Caregivers should assess each
patient/child according to the following criteria prior
to use:
• Patient/child sits in wheelchair
• Has no capacity to support herself/himself at all
• Cannot stand unsupported and is not able to bear
weight, not even partially
• Dependent on caregiver in most situations
• Physically demanding for caregiver
• Stimulation of remaining abilities is very important
Or, for a patient/child who:
• Is passive
• Might be almost completely bed ridden
• Often sti or contracted joints
• Totally dependent on the caregiver
• Physically demanding for caregiver
• Stimulation and activation is not a primary goal
Safe Working Load (SWL) for Paediatric clip sling:
• MAA4020M: 125 kg (275lbs).
The right type and size of slings should be used after
proper assessment of each patient/child size, condition
and the type of lifting situation.
If the patient/child does not meet these criteria, an
alternative equipment/system shall be used.
Expected Service Life
The expected service life of Paediatric clip sling is the
maximum period of useful life.
The expected life of the sling is dependent on the
actual use conditions. Therefore, before use, always
make sure that the sling does not show signs of
fraying, tearing or other damage and that there is no
damage (i.e. cracking, bending, breaking). If any such
damage is observed, do not use the sling. If you have
any doubts about sling safety, as a precaution and to
ensure safety, do not use the sling.
The expected service life of the Paediatric clip sling:
• Service Time: 2 years
• Shelf Time: 5 years
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4
Safety Instructions
WARNING
To avoid injury, make sure that the patient is
not left unattended at any time.
WARNING
To avoid injury, always assess the patient
prior to use.
WARNING
To avoid falling, make sure that the user
weight is lower than the safe working load
for all products or accessories being used.
WARNING
To avoid injury, never let the patient smoke
when using the sling. The sling can catch

WARNING
To avoid injury, only store the equipment for
a short period of time. If stored longer than
stated in the IFU, it can cause weakness
and breakage in the material.
WARNING
To avoid injury, keep the equipment away
from sun/UV-light. Exposure to sun/UV-light
can weaken the material.
Safety Practises
• At any time, if the patient becomes agitated, stop
transferring/transporting and safely lower the
patient.
• Patient with spasm can be lifted, but great care
should be taken to support the patient’s legs.
Serious incident
If a serious incident occurs in relation to this medical
device, aecting the user, or the patient then the user
or patient should report the serious incident to the
medical device manufacturer or the distributor. In
the European Union, the user should also report the
serious incident to the Competent Authority in the
member state where they are located.
ENEN

5
Parts Designation
Preparations
Before First Use (6 steps)
1. Check all parts of the sling, see section “Parts
Designation” on page 5. If any part is missing
or damaged, Do NOT use the sling.
2. Read this IFU thoroughly.
3. Check that the sling is clean.
4. Choose a designated area where the IFU should be
kept and easily accessible at all times.
5. Make sure to have a rescue plan ready in case of a
patient emergency.
6. For questions, contact your local Arjo
representative for support.
NOTE
Arjo recommends the name of the patient is
written on the sling care label to avoid cross
contamination between patients.
Before Every Use (6 steps)
1. Patient assessment must always determine the
methods used in everyday care, see “Intended
Use” on page 3.
WARNING
To avoid the patient from falling, make sure
to select the correct sling size according to
the IFU.
2. Make sure to select correct type and size of sling,
see “Sling Selection” on page 6.
3. Check the allowed combinations against the sling,
spreader bar and lift, see “Allowed Combinations”
on page 7.
WARNING
To avoid injury, always make sure to inspect
the equipment prior to use.
4. Check all parts of the sling, see “Parts
Designation” on page 5. If any part is missing
or damaged - Do NOT use the sling. Check for:
• fraying
• loose stitching
• tears
• fabric holes
• soiled fabric
• damaged clips
• unreadable or damaged label
WARNING
To prevent cross-contamination, always
follow the disinfection instructions in this
IFU.
5. Check that the sling is clean. If the sling is not
clean see “Cleaning and Disinfection” on page
12.
6. Before using the sling, read the lift IFU for
transfer/transport.
1. Stiener pocket
2. Sling label (located on the outside of the sling)
3. Buckle
4. Attachment clip
5. Leg strap
6. Leg ap
7. Body section
8. Shoulder strap
9. Head section
Example of slings. Not all models are represented.
1
3
4
5
8
6
7
9
2
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Fig. 1
Fig. 2
43 52 61 72.7 99.6 104.7 114.794.784.7
AB
COCCYX HEAD
cm
in
16,9 20.5 24 28.7 33.7 37.6 39.5 41.5 45.2
XXS XS SMLLLXL XXL
Select Sling Size
Using the Arjo Measuring Tape
(4 steps) (Accessory)
The Arjo Measuring Tape is a sizing accessory only
intended as a guide and is an approximation. Patient
width and body proportions should also be considered
when selecting the correct size of Arjo sling.
1. If possible, the patient should be in a seated
position.
2. Place the point marked A on the measuring tape
over the patient’s coccyx/against seat (position A).
(See Fig. 1) and (See Fig. 2)
3. Measure from coccyx/seat (position A) to the top
of the head (position B) (See Fig. 1).
4. The coloured area on the measuring tape that is
levelled with the top of the patient’s head indicates
the required sling size. If the sling size falls in
between two sizes, it is recommended to select the
smaller size. (See Fig. 2)
Sizing Without a Measuring Tape
(2 steps)
1. Place the sling over the patient’s back.
2. Make sure the sling covers the patient from the top
of the head (position B) to the coccyx (position A).
(See Fig. 1)
Sling Selection
The patient’s physical disabilities, weight distribution and general physique needs to be taken into consideration
when selecting a sling.
Article number Safe Working Load Product Description Size
MAA4020M 125 kg (275 lbs) Paediatric clip sling XXS, XS, S
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7
Allowed Combinations
WARNING
To avoid injury, always follow the allowed combinations listed in this IFU. No other
combinations are allowed.
Safe Working Load (SWL)
The SWL of the sling is at 125kg (275 lbs). Always follow the lowest SWL of the total system.
E.g. the Maxi Twin Compact lift/spreader bar has a SWL of 160 kg (352 lbs) and the MAA4020M sling has a
SWL of 125kg (275 lbs). This means that the sling has the lowest SWL. The patient is not allowed to weigh
more than the lowest SWL.
Lift Maxi Twin
Compact Maxi Lite Maxi 500 Maxi Twin
SWL 160 kg
(352 lbs)
160 kg
(352 lbs)
227
(500 lbs) 182 kg (401 lbs)
Spreader Bar
(DPS) Power Medium Flat Manual Manual Medium Power
Sling SWL Size Size Size Size Size
MAA4020M 125kg (275 lbs) S S S S S
Lift Maxi Move Maxi Sky
SWL 227kg (500 lbs) 272 kg (600 lbs)
Spreader Bar
(DPS)
Manual
Small
Manual
Medium
Power
Medium Manual Flat Power Medium
Sling SWL Size Size Size Size Size
MAA4020M 125kg (275 lbs) XXS, XS, S S S S S
Clip Attachment & Detachment
NOTE
If available on your lift device, reposition the
spreader bar using the Dynamic Position
System (DPS) for easier clip attachment of the
sling. See lift IFU for instructions.
Attach the Clips (5 steps)
1. Place the clip on the spreader bar lug. (See Fig. 3)
2. Pull the strap down.
3. Make sure the lug is locked at the top end of the
clip. (See Fig. 4)
4. Make sure the strap is not squeezed in between the
clip and the spreader bar.
5. Make sure the straps are not twisted.
Detach the Clips (3 steps)
Make sure that the weight of the patient is taken up by
the receiving surface before removing the clips.
1. Pull the strap up. (See Fig. 5)
2. Make sure the lug is unlocked at the bottom of the
clip.
3. Remove the clip.
Fig. 3 Fig. 4 Fig. 5
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Applying the Sling
In Bed (22 steps)
For transfer/transport/bathing, see respective lift IFU.
1. Place the lift nearby.
2. Apply bed brakes and adjust the height of the bed
to an ergonomic position, if possible.
3. The patient needs to lay down at on his/her back.
4. Check that the stieners are completely inside the
stiener pockets, if any.
5. Fold the sling lengthwise along the centre line,
outside facing outside. The sling label is located on
the outside.
WARNING
To avoid injury during log roll, make sure
there is another caregiver present and/or
use the side rails on the opposite side of
the bed.
6. Log roll the patient. (Use local technique.) If log
roll is not possible, use an Arjo sliding sheet/tube
for placing the sling. See respective Sliding Sheet/
Tube IFU
7. Place the folded sling over the patient’s side. Make
sure that the centre of the sling is aligned with the
patient’s spine, starting at the coccyx. Place the leg
aps towards the legs. (See Fig. 6)
8. Fold down the top of the sling and tuck it under the
patient’s body.
9. Log roll the patient to the other side.
10. Pull out the remaining part of the sling from under
the patient’s body.
11. Return the patient to his/her back.
12. Place the leg aps underneath the patient’s leg.
Place a pillow under the patient’s knees to ease the
attachment process of the leg clips.
13. Make sure that the: (See Fig. 7)
• sling is centred and at without creases,
• sling’s head support covers the neck/head area,
• sling pieces are not twisted underneath the
patient and
• all buckles are safely closed, if any
WARNING
To avoid injury, make sure the patient’s
arms are placed inside of the sling.
14. Make sure the patient’s arms are inside the sling.
15. Place the lift next to the patient and apply the
brakes.
WARNING
To avoid injury to the patient, pay close
attention when lowering or adjusting the
spreader bar.
16. Attach the sling. (See Fig. 4)
17. For easier attachment, make sure the spreader bar is
in a reclined position and if possible adjust the bed
to seated position.
18. Slightly lift the patient to create tension in the
sling. (See Fig. 8)
WARNING
To avoid the patient from falling, make sure
that the sling attachments are attached
securely before and during the lifting
process.
19. Make sure that all clips are attached securely and
the patient lays comfortably in the sling.
20. If an adjustment is needed, lower the patient and
make sure that the weight of the patient is taken up
by the receiving surface before removing the clip.
21. Release the brakes on the lift.
22. Transfer and transport according to the lift IFU.
In Chair/ Wheelchair (17 steps)
1. Place the lift nearby.
2. Apply the brakes on the wheelchair.
3. Check that the stieners are completely inside the
stiener pockets, if any.
4. Stand in front of the patient and lean the patient
forward.
Continue with the steps on the next page.
Fig. 6 Fig. 7 Fig. 8
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5. Place the sling over the patient’s back and head
with the inside of the sling against the patient. The
sling label is located on the outside.
6. Make sure that the centre of the sling is aligned
with the patient’s spine and coccyx.
7. Tuck in the end of the sling at the coccyx or against
the seat. If needed, use an Arjo sliding sheet/
tube for placing the sling under the patient. See
respective Sliding sheet/tube IFU
8. Lean the patient back.
9. Place the leg aps underneath the patient’s legs.
(See Fig. 9)
10. Make sure that the: (See Fig. 10)
• sling is centred and at without creases,
• sling’s head support covers the neck/head area,
• sling pieces are not twisted underneath the
patient
• all buckles are safely closed, if any
• patient’s arms are inside the sling.
WARNING
To avoid injury, make sure the patient’s
arms are placed inside of the sling.
11. Make sure the spreader bar is in a seated position
and place the lift in front of the patient with the lift
legs wide open.
12. Apply the brakes on the lift.
WARNING
To avoid injury to the patient, pay close
attention when lowering or adjusting the
spreader bar.
13. Attach the sling. If possible adjust the bed or
spreader bar to a seated position (for easier
attachment).
WARNING
Make sure straps are not caught by
wheelchair or lift castors.
14. Slightly lift the patient to create tension in the
sling. (See Fig. 11)
WARNING
To avoid the patient from falling, make sure
that the sling attachments are attached
securely before and during the lifting
process.
15. Make sure that all clips are attached securely and
the patient lays comfortably in the sling. . If an
adjustment is needed, lower the patient and make
sure that the weight of the patient is taken up by
the receiving surface before removing the clip.
(See Fig. 4)
16. Release the brakes on the lift.
17. Transfer/transport the patient according to the lift
IFU.
On Floor (31 steps)
1. Make a clinical assessment of the patient. Do not
use the sling if the patient has a head, neck, spine
or hip injury. Use a scoop stretcher instead. See the
Scoop Stretcher IFU.
2. Place a pillow under the patient’s head.
(See Fig. 12)
3. Make sure the patient is in an area that is accessible
for the lift. If needed, move the patient by using
an Arjo sliding sheet/tube. See respective Sliding
sheet/tube IFU.
4. Check that the stieners are completely inside the
stiener pockets, if any.
5. If the patient is able to sit up, continue to
next step. If not able to sit up, proceed to
step 9.
6. Patient able to sit up: Stand behind the patient
and help him/her to a seated position.
7. Place the sling over the patient’s back and head
with the inside of the sling against the patient. The
sling label is located on the outside.
8. Make sure that the centre of the sling is aligned
with the patient’s spine, starting at the coccyx or
against the seat. Continue to step 16.
9. Patient not able to sit up: Fold the sling
lengthwise along the centre of the sling, outside
facing outside. The sling label is located on the
outside.
Continue with the steps on the next page.
Fig. 9 Fig. 10 Fig. 11 Fig. 12
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10. Log roll the patient. (Use local technique)
(See Fig. 13) If log rolling is not possible, use an
Arjo sliding sheet/tube for placing the sling. See
respective Sliding sheet/tube IFU.
11. Place the folded sling over the patient’s side. Make
sure that the centre of the sling is aligned with the
patient’s spine, starting at the coccyx. Place the leg
 aps towards the legs.
12. Fold down the top of the sling and tuck it under the
patient’s body.
13. Log roll the patient to the other side. (Use local
technique)
14. Pull out the remaining part of the sling from under
the patient’s body.
15. Return the patient to his/her back.
16. Make sure that the: (See Fig. 14)
• sling is centred and  at without creases,
• sling’s head support covers the neck/head area,
• sling pieces are not twisted underneath the
patient
• all buckles are safely closed, if any
• patient’s arms are inside the sling.
WARNING
To avoid injury, make sure the patient’s
arms are placed inside of the sling.
17. Position the lift sideways with the lift legs wide
open. One caregiver needs to be close to the
patient’s head and the other caregiver needs to lift
up the patient’s legs.
18. Position one lift leg next to the patient’s head and
the other lift leg under the patient’s legs. Make sure
the spreader bar is positioned over the patient’s
shoulders. (See Fig. 15)
WARNING
To avoid injury to the patient, pay close
attention when lowering or adjusting the
spreader bar.
19. Lower the spreader bar with the Dynamic
Positioning System (DPS) in a reclined position.
20. Place the leg  aps underneath the patient’s legs.
Make sure the leg  aps are not twisted.
21. Attach the shoulder clips. (See Fig. 4)
22. Move the lift/spreader bar closer to the patient’s
legs.
23. Apply the brakes on the lift.
24. Attach the leg clips.
25. Slightly lift the patient to create tension in the
sling. (See Fig. 16)
WARNING
To avoid the patient from falling, make sure
that the sling attachments are attached
securely before and during the lifting
process.
26. Make sure that all clips are attached securely and
the patient lays comfortably in the sling. If an
adjustment is needed, lower the patient and make
sure that the weight of the patient is taken up by the
receiving surface before removing the clips.
27. Make sure that:
• the spreader bar is in a reclined position,
• one caregiver pays attention to the patient’s
head and.
• that the other caregiver holds up the patient’s
feet to prevent them from hitting the lift leg.
(See Fig. 16)
28. Remove the pillow.
29. Release the brakes on the lift
30. Bring the lift legs together.
31. Transfer/transport the patient according to the lift
IFU.
Fig. 13 Fig. 14 Fig. 15 Fig. 16
EN
EN

11
Removing the Sling
In Bed (12 steps)
1. Position the patient over the bed.(See Fig. 17)
2. Apply bed brakes and adjust the height of the bed
to an ergonomic position, if possible.
3. If the patient will be lowered on a at bed, make
sure the spreader bar is in a reclined position.
WARNING
To avoid injury to the patient, pay close
attention when lowering or adjusting the
spreader bar.
4. Lower the patient onto the bed. Make sure that the
weight of the patient is taken up by the receiving
surface before removing the clips.
5. Detach the sling. (See Fig. 5)
6. Move the lift away from the patient.
7. Pull out the leg aps from under the patient’s legs.
(See Fig. 14)
WARNING
To avoid injury during log roll, make sure
there is another caregiver present and/or
use the side rails on the opposite side of
the bed.
8. Log roll the patient. (Use local technique) If log
rolling is not possible, use an Arjo sliding sheet/
tube for removing the sling. See respective Sliding
sheet/tube IFU.
9. Tuck the sling under the patient’s body.
(See Fig. 18)
10. Log roll the patient to the other side and remove
the sling.
11. Return the patient to his/her back.
12. Make sure the patient is in a comfortable and
secure position in the bed.
In Chair/Wheelchair (13 steps)
1. Apply the brakes on the wheelchair.
2. Position the patient over the chair/wheelchair. Open
the lift legs if needed. (See Fig. 19)
3. Adjust the spreader bar to a seated position.
4. Lower the patient into the chair/wheelchair.
5. Make sure that the patient’s lower back is
positioned all the way in against chair/wheelchair
to prevent the patient from sliding out.
6. Position the patient by using the DPS.
WARNING
To avoid injury to the patient, pay close
attention when lowering or adjusting the
spreader bar.
7. Detach the sling. Make sure that the weight of the
patient is taken up by the receiving surface before
removing the clips. (See Fig. 5)
8. Release the brakes on the lift.
9. Move the lift away from the patient
10. Pull out the leg aps from under the patient’s legs
and place them backwards along the patient’s side.
(See Fig. 20).
11. Stand in front of the patient and lean the patient
forward.
12. Pull out the sling.
13. Lean the patient back up to a comfortable and
secure position.
Fig. 17 Fig. 18 Fig. 19 Fig. 20
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12
Cleaning and Disinfection
WARNING
To prevent cross-contamination, always
follow the disinfection instructions in this
IFU.
WARNING
To avoid material damage and injury, clean
and disinfect according to this IFU.
• No other chemicals are allowed.
• Never clean with chlorine.
• Chlorine will deteriorate the surface of
the material.
WARNING
To avoid injury, always remove the sling
before disinfecting the lift.
All Paediatric Slings should be cleaned when they are
soiled or stained and between patients.
Cleaning Instruction (5 steps)
1. Detach the sling from the lift.
2. Before washing close the buckles.
3. Machine wash the sling at 70°C (158°F). In order
to obtain sucient level of disinfection, please
wash according to local hygiene legislation.
4. If allowed according to the product label, tumble
dry in low temperature, maximum 60°C (140°F).
5. Do NOT
• wash with rough surfaces or sharp objects
• use any mechanical pressure, pressing or roiling
during the washing and drying process
• use bleach
• use gas sterilization
• use autoclave
• dry clean
• Steam
• ironing
Cleaning Chemicals
For all sling material use common commercial
detergent without optical brightener.
No other chemicals are allowed e.g. chlorine, softener,
iodine based disinfectants, bromine and ozone.
Disinfection
The only allowed disinfection is disinfection by
washing.
Care and Preventive Maintenance
WARNING
To avoid injury to both patient and
caregiver, never modify the equipment or
use incompatible parts.
Before and After Every Use
Visually check all exposed parts
The caregiver shall inspect the sling before and after
every use. The complete sling should be checked for
all deviations listed below. If any of these deviations
are visible, replace the sling immediately.
• Fraying
• Loose stitching
• Tears
• Holes
• Discolouration and stains from bleaching
• Sling soiled or stained
• Unreadable or damaged label
When Soiled or Stained and Between
Patients
Clean/Disinfect
The caregiver should make sure that the sling is
cleaned according to “Cleaning and Disinfection” on
page 12, when it is soiled or stained and between
patients.
Storage
When not in use, the slings should be stored away
from direct sunlight where they are not subject to
unnecessary strain, stress or pressure, or to excessive
heat or humidity. The slings should be kept away from
sharp edges, corrosives or other things that could cause
damage on the sling.
Service and Maintenance
It is recommended that qualied personnel inspect the
condition of the sling twice a year (every 6 month),
according to ISO 10535.
ENEN

13
Troubleshooting
Problem Action
The patient is not positioned correctly in
the sling (e.g. one strap is shorter than the
other).
• Make sure the clip straps are not twisted.
• Make sure the patient is seated on the inside of the
sling. The outside has a label for reference.
• Make sure the patient is centred in the sling.
The patient feels discomfort in the leg area
when seated in the sling.
Make sure that there are no creases on the leg aps of
the sling.
The sling is di󰀩cult to apply (e.g. during
log roll).
Use an Arjo sliding sheet/tube according to instructions
in respective IFU.
There are di󰀩culties applying the shoulder
clips.
• Place the patient in a more seated position in the bed
or on the oor. Place a pillow behind the patient’s
neck/back, outside of the sling.
• Raise the back rest of the bed, if available.
• Make sure the clip strap is not caught between the lug
on the lift and the clip attachment.
• Adjust the spreader bar to e more reclined position.
Pay attention to the patient’s head.
There are di󰀩culties applying the leg clips.
• Bend the patient’s legs or place a pillow under the
patient’s knees. If the sling is applied on the oor,
place the patient’s legs on the caregiver’s knee.
• Make sure the clip strap is not caught between the lug
on the lift and the clip attachment.
• Adjust the spreader bar to a more seated position.
It is di󰀩cult to use the sling in combination
with the lift and spreader bar.
Use the sling only in accordance with the combinations
described in section “Allowed Combinations” on page
7.
The position of the patient in the sling
should be more reclined or seated. Use the spreader bar to adjust the patient’s position.
The patient wishes to have extra support
for the neck. Place a pillow behind the patient’s neck, inside the sling.
The head is not supported by the sling. Make sure the head section of the sling is buckled
together with the shoulder section of the sling.
ENEN

14

General
Safe working load (SWL) = Maximum patient
weight See “Allowed Combinations” on page 7
Service life – Recommended period of use 2 years*
*Refer to “Expected Service Life” on page 3.
Shelf life – Maximum period of storing new
unpacked product 5 years
Model and Type See “Sling Selection” on page 6
Operating, Transport and Storage Environment
Temperature 0°C to +40°C (+32°F to +104°F) Operating and Storage
-25°C to +60°C (+13°F to +140°F) Transport
Humidity Max 15–70% at +20°C (68°F) Operating and Storage
Max 10–95% at +20°C (68°F) Transport
End of Life Disposal
Package The bag consists of soft plastic, recyclable to local
legislations.
Sling
Slings including sti󰀨eners/stabilizers, padding material,
any other textiles or polymers or plastic materials etc.
should be sorted as combustible waste.
Parts and Accessories
Measuring tape MTA1000
ENEN

15
Label on the Sling
Care and Washing Symbols
Machine wash 70°C (158°F)
No bleaching allowed
No tumble drying allowed
Tumble drying
No Ironing allowed
No dry cleaning allowed

CE marking indicating conformity with
European Community harmonised
legislation
Indicates the product is a Medical
Device according to EU Medical Device
Regulation 2017/745
Unique device identier
Symbol for Clip
Use a clip spreader bar.
Fibre Content
PES Polyester
PU Polyurethane
Article Number
REF
XXXXXX-X
Article number with -X refers
to the sling size.
REF
XXXXXXX
If the article number is stated
without the size letter at the end,
it means the sling is a One Size.
Misc. Symbols
Safe Working Load (SWL)
Patient’s name symbol
Single patient multiple use
Record symbol
Read the IFU before use
REF Article number
Manufacturing date and year
Manufacturer name and address
UK Symbol explanation
This section is only applicable to United Kingdom (UK) market when UK marking is applied to the
Arjo medical device labelling.
UK marking indicating conformity with UK Medical Devices
Regulations 2002 (SI 2002 No 618, as amended)
UK Responsible Person & UK Importer:
Arjo (UK) Ltd, ArjoHuntleigh House, Houghton Regis. LU5 5XF
Is the appointed UK Responsible Person as dened in UK Medical Devices Regulations 2002
(SI 2002 No 618, as amended).
For Northern Ireland (NI) CE marking will still apply until further amendment to applicable regulations.
ENEN

16
警告
为避免受到伤害，在使用产品前，必须阅读本使用说明书以及产品随附的文档。请务必阅读本使用
说明书。
设计政策和版权
带® 与™ 的标志是 Arjo 企业集团的商标。
© Arjo 2022.
我们的宗旨是不断进行改进，因此我们保留更改设计的权利，恕不另行通知。未经 Arjo 同意，不得全部或部分复制本出版
物中的内容。
前言
感谢您购买 Arjo 设备。请通读本 使用说明书 (IFU) ！
Arjo 对任何因未经授权改动产品而导致的意外、事故或性能丧失均不承担任何责任。
客户支持
如果需要更多信息，请联系您当地的 Arjo 代表。联系信息位于本 IFU 的结尾。
本使用说明书 (IFU) 中的定义
警告 表示：安全性警告。如不理解并且不遵守该警告可能会对您或他人造成人身伤害。
注意事项 表示：如不遵守这些说明可能导致整个系统或设备或其中部分部件的损坏。
注意 表示：这些是正确使用本系统或设备的重要信息。
目录
前言 ...................................................................16
客户支持................................................................16
本使用说明书 (IFU) 中的定义 ................................16
既定用途 ............................................................17
患者/儿童评估........................................................17
预计使用寿命.........................................................17
安全说明 ............................................................18
安全规范................................................................18
严重事件................................................................18
部件名称 ............................................................19
使用准备 ............................................................19
初次使用前（6 个步骤）...........................................19
每次使用前（6 个步骤）...........................................19
选择吊兜规格.....................................................20
使用 Arjo 测 尺（ 4 个步骤）（附件）...........................20
不使用测尺测量（2 个步骤）....................................20
选择吊兜 ............................................................20
允许组合 ............................................................21
安全承重 (SWL).....................................................21
连接与拆除卡扣 .................................................21
连接卡扣（5 个步骤）..............................................21
拆除卡扣（3 个步骤）..............................................21
应用吊兜 ............................................................22
在床上（22 个步骤）................................................22
在座椅/轮椅上（17 个步骤）....................................22
在地板上（31 个步骤）............................................23
拆除吊兜 ............................................................25
在床上（12 个步骤）................................................25
在座椅/轮椅上（13 个步骤）....................................25
清洁和消毒.........................................................26
清洁说明（5 个步骤）..............................................26
清洁用化学品.........................................................26
消毒 .......................................................................26
保养与防护性维护..............................................26
每次使用前后.........................................................26
变脏/染污或用于其他患者时 ..................................26
贮存 .......................................................................26
保养和维护 ............................................................26
故障排除 ............................................................27
技术规格 ............................................................28
吊兜上的标牌.....................................................29
使用说明书
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既定用途
儿科专用卡扣式吊兜是一款辅助产品，旨在帮助转
运行动能力受限，并且在转运时需要全面支撑身体
的儿科患者/儿童。
儿科专用卡扣式吊兜仅供对护理环境有充分了解，
并遵守使用说明书中说明的训练有素的护理人员
使用。
儿科专用卡扣式吊兜适用于儿童。
儿科专用卡扣式吊兜适合在医院环境、护理中心、其
他健康护理机构和家庭中使用。
儿科专用卡扣式吊兜只能用于本使用说明书中指定
的用途。禁止用于其他目的。
患者/儿童评估
我们建议使用机构建立日常评估程序。护理人员应
在使用本装置前根据以下标准评估每名患者/儿童：
• 患者/儿童坐在轮椅内
• 完全没有能力支撑自己的身体
• 不能自行站立，也无法承受自己的体重（甚至部
分体重）
• 在大部分情况下依赖护理人员
• 身体需要依赖护理人员
• 刺激剩余能力非常重要
或者用于符合以下条件的患者/儿童：
• 依靠他人
• 几乎卧床不起
• 关节经常僵直或挛缩
• 完全依靠护理人员
• 身体需要依赖护理人员
• 刺激和活化不是主要目标
儿科专用卡扣式吊兜的安全承重 (SWL)：
• MAA4020M：125 kg (275lbs)
正确评估每名患者/儿童的体型、状况和移位环境
后，应使用适合的吊兜类型和规格。
如果患者/儿童不能满足这些条件，应使用其他的设
备/系统产品。
预计使用寿命
儿科专用卡扣式吊兜的预计使用寿命为最长使用寿
命期限。
吊兜的预计使用寿命取决于实际使用条件。因此在
使用之前，务必确保吊兜未出现磨损、撕裂或其他损
坏迹象，并且未发生损坏（即：裂口、弯曲、断裂）。如
果看到任何此类损坏情况，请勿使用吊兜。如果对于
吊兜安全有任何疑问，作为预防措施并为了确保安
全，请勿使用吊兜。
儿科专用卡扣式吊兜的预计使用寿命：
• 使用时间：2 年
• 保质期：5 年
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18
安全说明
警告
为避免人身伤害，应始终有专人看护患者。
警告
为避免人身伤害，应在使用前始终对患者状况进
行评估。
警告
为避免摔倒，患者体重不得超出所用产品及附件
的安全工作负荷。
警告
为避免人身伤害，切勿在使用吊兜时让患者吸烟。
吊兜会导致火灾。
警告
为避免人身伤害，仅应短期存储设备。如果存储时
间超过 IFU 中规定的时间，则会导致材料断裂和
强度变弱。
警告
为避免人身伤害，请避免阳光/紫外光照射到设
备。暴露于阳光/紫外光会降低材料强度。
安全规范
• 当患者变得烦躁不安时，随时停止转运/运送并
安全地放低患者。
• 痉挛患者可以吊升，但应特别注意支托患者的
双腿。
严重事件
如果发生与该医疗器械相关并影响用户或患者的严
重事件，则用户或患者应将该严重事件报告给医疗
器械制造商或分销商。在欧盟，用户还应向其所在成
员国的主管当局报告该严重事件。 ZHZH

19
部件名称
使用准备
初次使用前（6 个步骤）
1. 检查吊兜的所有部件，请参阅 第19 页的“部件
名称” 一节。如果任何部件缺失或损坏，请勿使用
吊兜。
2. 仔细阅读本 IFU。
3. 检查吊兜是否干净。
4. 在指定位置妥善存放 IFU，以便随时取阅。
5. 确保制定好抢救计划以防患者出现紧急情况。
6. 有关任何问题，请联系您当地的 Arjo 代表以寻求
支持。
注意
Arjo 建议将患者姓名标注在吊兜保养标牌上，避
免患者之间交叉感染。
每次使用前（6 个步骤）
1. 对患者评估时，必须始终确定日常护理中使用的
方法，请参阅 第17 页的“既定用途” 。
警告
为避免患者坠落，请务必根据 IFU 选择正确的吊
兜尺寸。
2. 确保选择正确的吊兜类型和规格，请参阅
第20 页的“选择吊兜” 。
3. 检查吊兜、吊架和移位机的允许组合，请参阅
第21 页的“允许组合” 一节。
警告
为避免人身伤害，请始终确保在使用前检查设备。
4. 检查吊兜的所有部件，请参阅
第19 页的“部件
名称” 一节。如果任何部件缺失或损坏 —不得使
用吊兜。检查：
• 磨损
• 松散缝合
• 裂口
• 破洞
• 布料染污
• 损坏的卡扣
• 标牌无法辨认或损坏
警告
为了防止交叉感染，必须始终遵守本 IFU 中的消
毒说明。
5. 检查吊兜是否干净。如果吊兜不干净，请参阅
第26 页的“清洁和消毒” 。
6. 使用吊兜之前，请阅读移位机 IFU 了解转运/运
输说明。
1. 加强板袋
2. 吊兜标牌（位于吊兜外部）
3. 带扣
4. 连接卡扣
5. 腿带
6. 腿皮瓣
7. 身体部分
8. 肩带
9. 头部
吊兜示例。未示出所有型号。
1
3
4
5
8
6
7
9
2
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20
图
1
图2
43 52 61 72.7 99.6 104.7 114.794.784.7
AB
COCCYX HEAD
cm
in
16,9 20.5 24 28.7 33.7 37.6 39.5 41.5 45.2
XXS XS SMLLLXL XXL
选择吊兜规格
使用 Arjo 测 尺（ 4 个步骤）（附件）
Arjo 测尺是一种仅供参考的测量附件，提供估算值。
选择正确规格的 Arjo 吊兜时，还应考虑患者体宽和
身材比例。
1. 如果可能，应让患者处于坐姿。
2. 将测尺上标记 A的测点置于患者的尾骨处/顶靠
座位（位置 A）。（请见图 1）和（ 请 见 图 2）
3. 测量从尾骨/座位（位置 A）到头顶（位置 B）之 间
的长度（请见图 1）。
4. 测尺上与患者头顶平齐的彩色区域指示出所需
的吊兜规格。如果指示的吊兜规格介于两个规格
之间，则建议选择较小规格。（请见图 2）
不使用测尺测量（2 个步骤）
1. 将吊兜置于患者背部。
2. 确保吊兜覆盖患者头顶（位置 B）至 尾 骨（ 位
置A）之间的部位。（请见图 1）
选择吊兜
选择吊兜时，需要考虑患者的肢体残疾、体重分布和总体形。
料号 安全承重 产品说明 规格
MAA4020M 125 kg (275 lbs) 儿科专用卡扣式吊兜 XXS, XS, S
使用测尺测量长度
ZHZH