Arjo MAA1150 User manual

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使用说明书 · Bedienungsanleitung · Mode d’emploi · Istruzioni per l’uso · Gebruiksaanwijzing
INSTRUCTIONS FOR USE
Stretcher Slings
04.SS.00-INT1_704.SS.00-INT1_7
••
10/202210/2022

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/Resident 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(7steps) .....................................5
After last use ...........................................................5
Sling Selection.....................................................6
Transfer/Transport/Toileting.....................................6
Bathing ....................................................................6
Allowed Combinations.........................................6
SafeWorkingLoad(SWL).......................................6
Loop Attachment & Detachment..........................7
AttachtheLoops(5Steps)......................................7
DetachtheLoops(2steps) .....................................7
Applying the Sling................................................7
InBed(21steps).....................................................7
OnFloor(28steps) .................................................8
Removing the Sling ...........................................10
InBed(11steps) ...................................................10
Cleaning and Disinfection..................................11
CleaningInstruction(4steps) ............................... 11
Disposable Sling – Do NOT wash......................... 11
Cleaning Chemicals .............................................. 11
Disinfection............................................................ 11
Care and Preventive Maintenance ....................12
BeforeandAfterEveryUse...................................12
When Soiled, Stained and Between Patients........12
Storage..................................................................12
Service and Maintenance......................................12
Troubleshooting.................................................13
TechnicalSpecications ....................................13
Label on the Sling..............................................14

ENEN

3
Intended Use
Stretcherslingisspecicallydesignedtotransfer
a patient/resident in a supine position. This
product is intended for assisted lateral transfer
of patients/residents with limited ability to move.
The Stretcher sling should be used together
with Arjo lift devices and Arjo stretcher frames
in accordance with the Allowed Combinations
speciedintheInstructionforUse(IFU).
Product MAA1152 made of Mesh material is also
intended for bathing.
Disposable stretcher sling is intended for assisted
lateral transfer of patients/residents with limited
ability to move while using a patient/resident
transfer lifter, under the supervision of trained
nursingsta󰀨.Disposablestretcherslingistobe
used for a limited period only, and, by nature of
their design, must be treated as a disposable
andpatient/residentspecicproduct.Disposable
stretcher sling should be used together with
Arjo lift devices in accordance with the Allowed
CombinationsspeciedintheIFU.
Disposable stretcher sling must not be used to
support a resident while bathing or showering.
Disposable stretcher sling cannot be washed.
The Stretcher sling/Disposable stretcher 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.
The Stretcher sling/Disposable stretcher sling is
intended to be used in hospital environments,
nursing homes, other healthcare facilities and
home care.
The Stretcher sling/Disposable stretcher sling
shouldonlybeusedforthepurposespecied
inthisInstructionsforUse.Anyotheruseis
prohibited.
Patient/Resident Assessment
We recommend that facilities establish regular
assessment routines. Caregivers should assess
each patient/resident according to the following
criteria prior to use:
• Patient/resident is passive
• Might be almost completely bed ridden
• Oftensti󰀨orcontractedjoints
• Totally dependent on the caregiver
• Physically demanding for the caregiver
• Stimulation and activation is not a primary
goal
SafeWorkingLoad(SWL)forStretchersling:
• MAA1151, MAA1150, MAA1152: 272 kg
(600lbs).
SafeWorkingLoad(SWL)forDisposable
stretcher sling:
• MFA5000:272kg(600lbs).
The right type and size of slings should be used
after proper assessment of each patient/resident’s
size, condition and the type of lifting situation.
If the patient/resident does not meet these criteria
an alternative equipment/system shall be used.
Expected Service Life
The expected service life of Stretcher sling/
Disposable stretcher 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
any sign 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.
The expected service life of the Stretcher sling/
Disposable stretcher sling:
Service Time:
• 2years(Stretchersling)
• Disposablesling:2weeks(basedon
4transfersperday)(Disposablestretcher
sling)
Shelf Time:
• 5years(Stretchersling/Disposable
stretchersling)
ENEN

4
Safety Instructions
WARNING
To avoid injury, make sure that the patient is
not left unattended at any time.
WARNING
To avoid injury, never wash a disposable
sling. A disposable sling is only intended
for “single patient use”.
WARNING
To avoid injury, always assess the patient
prior to use.
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 falling, ensure 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, 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 (7 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. Check the allowed combinations against the sling,
spreader bar and lift, see “Allowed Combinations”
on page 6.
WARNING
To avoid injury, always make sure to inspect
the equipment prior to use.
3. 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
• thread breakage
• tears
• fabric holes
• soiled fabric
• damaged loops
• unreadable or damaged label
WARNING
To prevent cross-contamination, always
follow the disinfection instructions in this
IFU.
4. Check that the sling is clean. If the sling is
not clean see”Cleaning and Disinfection” on
page 11.
5. Always check the washing symbol on the
disposable sling’s label. If the disposable sling has
been washed, throw the disposable sling away. See
“Disposable Sling – Do NOT wash” on page 11.
6. If this symbol appears, do NOT use the
disposable sling. The label indicates that
the disposable sling has been washed.
7. Before using the sling, read the lift IFU for transfer,
transport and bathing.
After every use
If the patient is leaving the hospital, throw away the
patient specic disposable sling.
1. Sling label (located on the outside of the sling)
2. Do not wash label (On Disposable stretcher sling
only, located on the outside of the sling)
3. Strap with loops
4. Commode hole (certain slings only)
5. Foot end
6. Head end
Example of slings. Not all models are represented.
34
5
1
2
6
1
3
5
6ENEN

6
Sling Selection
The patient’s physical disabilities, weight distribution and general physique needs to be taken into consideration
when selecting a sling.
Select the Stretcher sling size by measuring against the patient‘s head and feet. Make sure to select the right size
to avoid the patient’s feet from falling out of the sling.
Transfer/Transport/Toileting
Article
number
Safe Working
Load Product Description Size
MAA1151 272kg(600lbs) Loop stretcher sling L(1610mm),XL(1650mm)
MAA1150 272kg(600lbs) Loop stretcher sling – commode
aperture L(1610mm),XL(1650mm)
MFA5000 272kg(600lbs) Disposable loop stretcher sling Onesize(1740mm)
Bathing
Article
number
Safe Working
Load Product Description Size
MAA1152 272kg(600lbs) Loop bathing stretcher sling –
commode aperture L(1610mm),XL(1650mm)
Allowed Combinations
WARNING
To avoid injury, always follow the allowed combinations listed in this IFU. No other
combinations are allowed.
Safe Working Load (SWL)
Always follow the lowest SWL of the total system. E.g. the Maxi Move lift has a SWL of 160 kg (352 lbs) and
the MAA1151 sling has a SWL of 272 kg (599 lbs). This means that the Maxi Move lift has the lowest SWL. The
patient is not allowed to weigh more than the lowest SWL.
Lift Maxi Move MaxiSky600 Maxi Sky 2
SWL 160kg(352lbs) 272kg(600lbs) 272kg(600lbs)
Spreader Bar Stretcher Frame
700-19302
Stretcher Frame
700-19522
Stretcher Frame
700-15695
Sling SWL Size Size Size
MAA1150 272kg(600lbs) L,XL L,XL L,XL
MAA1151 272kg(600lbs) L,XL L,XL L,XL
MAA1152 272kg(600lbs) L,XL L,XL L,XL
MFA5000 272kg(600lbs) One Size One Size One Size
ENEN

7
Applying the Sling
In Bed (21 steps)
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. 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.
5. 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
6. Place the folded sling over the patient’s side.
7. Fold down the top of the sling and tuck it under
the patient’s body. If a stretcher commode sling is
used make sure the commode hole is positioned
correctly. (See Fig. 4)
8. Log roll the patient to the other side.
9. Pull out the remaining part of the sling from under
the patients body.
10. Return the patient to his/her back.
11. Make sure that the: (See Fig. 5)
• sling is centred and at without creases,
• sling’s head end covers the patient’s head area,
• sling pieces are not twisted underneath the
patient and
• if a stretcher commode sling is used make sure
the commode hole to positioned correctly
WARNING
To avoid injury, make sure the patient’s
arms are placed inside of the sling.
Continue with the steps on the next page.
Loop Attachment & Detachment
Attach the Loops (5 Steps)
1. Place the loop over the spring loaded latch (A).
(See Fig. 1)
2. Pull the loop down to force the latch to open.
3. Make sure that the spring loaded latch closes
completely with the loop inside. (See Fig. 1)
4. Make sure that the latch is moving freely.
5. Make sure loops and straps are not twisted.
TIPS
Usetheshorterlooplengthsforlessswingin
the sling.
Detach the Loops (2 steps)
Make sure that the weight of the patient is taken up by
the receiving surface before removing the loop.
Method 1
1. Press the spring loaded latch open.
2. Remove the loop.
Method 2
1. Pull one side of the loop over the hook and spring
loaded latch. (See Fig. 2)
2. Pull down the loop. (See Fig. 3)
Fig. 1
A
Fig. 2 Fig. 3 Fig. 4
ENEN

8
WARNING
To avoid injury to the patient, pay close
attention when lowering or adjusting the
spreader bar.
12. Position the stretcher bar over the patient.
(See Fig. 6)
13. Start by attaching the loops at each side of the
patient’s hip area. Make sure the mid part of
the sling covers the patient’s hip area for better
comfort. (See Fig. 1)
TIPS
Usetheshorterlooplengthsforlessswingin
the sling.
14. Finally attach the remaining loops starting from
the head area. Make sure to attach each loop at the
same loop length as the one across.
15. If medical condition permits, raise the patient’s
head for better comfort by using a dierent loop
length.
16. Slightly lift the patient to create tension in the
sling. (See Fig. 7)
WARNING
To avoid the patient from falling, make sure
that the sling attachments are securely
attached before and during the lifting
process.
17. Make sure that:
• All loops are securely attached
• The patient lays comfortably in the sling.
18. 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 loops.
19. Adjust the balance of the stretcher frame, if needed.
See respective Lift IFU.
20. If a stretcher commode sling is used, a bed pan can
be placed under the patient, if needed.
21. Transfer the patient. See respective lift IFU.
On Floor (28 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. (Follow local routine.) Use a scoop
stretcher instead. See the Scoop Stretcher IFU.
2. Place a pillow under the patient’s head. (See Fig. 8)
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. Fold the sling lengthwise along the centre line,
outside facing outside. The sling label is located on
the outside.
5. 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.
6. Place the folded sling over the patient’s side. Make
sure that the centre line is aligned with the patient’s
spine. (See Fig. 9)
7. Fold down the top of the sling and tuck it under the
patient’s body.
8. Log roll the patient to the other side.
9. Pull out the remaining part of the sling from under
the patients body.
Continue with the steps on the next page.
Fig. 5
Fig. 6 Fig. 7
Fig. 8 Fig. 9
ENEN

9
10. Return the patient to his/her back.
11. Make sure that the: (See Fig. 10)
• sling is centred and at without creases,
• sling’s head end covers the patient’s head area,
• sling pieces are not twisted underneath the
patient and
• if a stretcher commode sling is used make sure
the commode hole to positioned correctly
WARNING
To avoid injury, make sure the patient’s
arms are placed inside of the sling.
12. Position the lift sideways with the lift legs wide
open.
13. One caregiver needs to be close to the patient’s
head and the other caregiver needs to lift up the
patient’s legs.
14. Position one lift leg next to the patient’s head and
the other lift leg under the patient’s legs. Make sure
the stretcher frame is positioned over the patient’s
shoulders. (See Fig. 11)
15. Apply the brakes on the lift.
WARNING
To avoid injury to the patient, pay close
attention when lowering or adjusting the
spreader bar.
16. Lower the stretcher frame.
17. Start by attaching the loops at each side of the
patient’s hip area. Make sure the mid part of
the sling covers the patient’s hip area for better
comfort. (See Fig. 1)
TIPS
Usetheshorterlooplengthsforlessswingin
the sling.
18. Finally attach the remaining loops starting from
the head area. Make sure to attach each loop at the
same loop length as the one across.
19. If medical condition permits, raise the patient’s
head for better comfort by using a dierent loop
length.
20. Slightly lift the patient to create tension in the
sling. (See Fig. 12)
WARNING
To avoid the patient from falling, make sure
that the sling attachments are attached
securely before and during the lifting
process.
21. Make sure that:
• All loops are securely attached
• The patient lays comfortably in the sling.
22. 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 loops.
23. Adjust the balance of the stretcher frame, if needed.
See respective Lift IFU.
24. Continue to lift up the patient.
25. Remove the pillow.
26. Release the brakes on the lift.
27. Bring the lift legs together.
28. Transport the patient. See respective lift IFU.
Fig. 10 Fig. 11 Fig. 12
ENEN

10
Removing the Sling
In Bed (11 steps)
1. Position the patient over the bed. (See Fig. 13)
2. Apply bed brakes and adjust the height of the bed
to an ergonomic position, if possible.
3. Make sure the bed is in a at 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.
5. Detach the sling, make sure all straps are detached.
(See Fig. 14)
6. Move the lift away from the patient.
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.
7. 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
8. Tuck the sling under the patient’s body.
9. Log roll the patient to the other side and remove
the sling.
10. Return the patient to his/her back.
11. Make sure the patient is in a comfortable and
secure position in the bed.
Fig. 13 Fig. 14
ENEN

11
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.
WARNING
To avoid injury, never wash a disposable
sling. A disposable sling is only intended
for “single patient use”.
All Stretcher slings, except the disposable stretcher
slings should be cleaned when they are soiled or
stained and between patients.
Cleaning Instruction (4 steps)
(NOT disposable sling)
1. Detach the sling from the lift.
2. Check the symbols on the product label for
cleaning recommendations.
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.
If allowed according to the product label, tumble
dry in low temperature, max 60°C (140°F).
4. Do NOT
• wash with rough surfaces or sharp objects
• use any mechanical pressure, pressing or rolling
• use bleach
• use gas sterilization
• use autoclave
• dry clean
• steam
• ironing
Disposable Sling – Do NOT wash
The disposable sling is for single patient use.
Do NOT clean, wash, disinfect, wipe or sterilize the
disposable sling. If the disposable sling has been
subjected to any such treatment, it shall be discarded.
The disposable sling is marked with the “Do NOT
wash” label. (See Fig. 15)
If the disposable sling is washed, the “Do NOT use/
lift” label will appear. (See Fig. 16)
Cleaning Chemicals
(NOT disposable sling)
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.
This does not apply to disposable slings. Do NOT
clean, wash or disinfect a disposable sling.
Fig. 15 Fig. 16
ENEN

12
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
• For disposable slings: Make sure the “Do NOT
wash” symbol on the head support is intact.
If damaged or missing and the underlying red
“Do NOT use/lift” symbol appears, replace the
sling immediately. See “Label on the Sling” on
page 14.
When Soiled, Stained and Between
Patients
Clean/Disinfect, all slings except the
disposable slings
The caregiver should make sure that the sling is
cleaned according to “Cleaning and Disinfection” on
page 11, when it is soiled or stained and between
patients.
Disposable slings
Washing or disinfection is not allowed. Do not wipe,
sterilize or soil the disposable sling. If the disposable
sling has been subjected to any treatment, it shall be
discarded.
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.
• Make sure that both shoulder loops are attached at
the right length.
• Make sure the straps are not twisted.
• Make sure the patient is positioned 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 when using
the sling.
• Make sure that there are no creases on the fabric.
• Make sure that both shoulder loops are attached at
the right length.
Itisdi󰀩culttousetheslingincombination
with the lift.
Usetheslingonlyinaccordancewiththecombinations
described in section “Allowed Combinations” on
page 6.
The position of the patient in the sling
should be more reclined or upward. Usethelooplengths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.
For MFA5000: The Disposable stretcher
sling is soiled, stained or wet.
Throw the disposable sling away and replace it with a
new one.
For MFA5000: The “Do NOT wash” label is
damaged or missing and the underlying red
symbol appears
Throw the disposable sling away and replace it with a
new one.

General
Safeworkingload(SWL)=Maximumtotalload See “Allowed Combinations” on page 6.
Service life – Recommended period of use
Disposable sling: 2 weeks, based on 4 transfers/
day*
All other slings: 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 15–70%at+20°C(68°F)OperatingandStorage
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.
ENEN

14
Label on the Sling
Care and Washing Symbols
Machinewash70°C(158°F)
No bleaching allowed
No tumble drying allowed
Tumble drying
Does not apply to disposable slings
No Ironing allowed
Do NOT wash the disposable sling
Only applies to disposable slings
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
Disposable Sling Symbols
“Do NOT wash” symbol. Located on the
outside of the sling.
“Do NOT use/lift” symbol. The
disposable sling has been washed.
Located on the outside of the sling.
Symbol for Loop
Usealoopspreaderbar.
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.
Fibre Content
PES Polyester
PU Polyurethane
PP Polypropylene
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

15
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。联系信息在本 使用说明书 (IFU) 的最后一页列出。
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 ...................................................................15
客户支持................................................................15
本使用说明书(IFU)中的定义 ................................15
既定用途 ............................................................16
患者/被照护人评估 ................................................16
预计使用寿命.........................................................16
安全说明 ............................................................17
安全规范................................................................17
严重事件................................................................17
部件名称 ............................................................18
使用准备 ............................................................18
初次使用前（6个步骤）...........................................18
每次使用前（7 个步骤）...........................................18
每次使用后 ............................................................18
选择吊兜 ............................................................19
转运/如厕...............................................................19
淋浴 .......................................................................19
允许组合 ............................................................19
安全承重(SWL).....................................................19
连接和拆除环扣 .................................................20
连接环扣（5 个步骤）..............................................20
拆除环扣（2 个步骤）..............................................20
应用吊兜 ............................................................20
在床上（21 个步骤）................................................20
在地板上（28个步骤）............................................21
拆除吊兜 ............................................................23
在床上（11 个步骤）................................................23
清洁和消毒.........................................................24
清洁说明（4 步）......................................................24
一次性吊兜 – 请勿清洗..........................................24
清洁用化学品.........................................................24
消毒 .......................................................................24
保养与防护性维护..............................................25
每次使用前后.........................................................25
弄脏或沾污以及患者之间互用时............................25
贮存 .......................................................................25
保养和维护 ............................................................25
故障排除 ............................................................26
技术规格 ............................................................26
吊兜上的标牌.....................................................27
使用说明书
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既定用途
担架式吊兜专为转运处于仰卧位的患者/被照护人
而设计。此产品适用于对行动能力受限的患者/被照
护人进行辅助侧向转运。应按照本使用说明书(IFU)
中指定的允许组合，将担架式吊兜与 Arjo 移位机和
Arjo 担架吊架配合使用。
产品 MAA1152 采用网状材料制成，还适用于沐浴。
一次性担架式吊兜适合在经过培训的护理人员的监
督下，一边使用患者/被照护人转运移位机，一边对
行动能力受限的患者/被照护人进行辅助侧向转运。
一次性担架式吊兜只能在有限期限内使用，由于其
设计性质，必须将其作为患者/被照护人专用一次性
产品进行处理。应按照本使用说明书 (IFU) 中指定
的允许组合，将一次性担架式吊兜与 Arjo 移位机配
合使用。
一次性担架式吊兜不得用于支撑正在洗浴或淋浴的
被照护人。一次性担架式吊兜不可洗涤。
担架式吊兜/一次性担架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。
担架式吊兜/一次性担架式吊兜适用于医院、护理中
心、其他健康护理机构和家庭护理。
担架式吊兜/一次性担架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/被照护人评估
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条件评估每名患者/被照
护人：
• 患者/被照护人依靠他人
• 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
担架式吊兜的安全承重(SWL)：
• MAA1151、MAA1150、MAA1152：
272kg(600lbs)
一次性担架式吊兜的安全承重(SWL)：
• MFA5000：272kg(600lbs)
正确评估每名患者/被照护人的体型、状况和移位环
境类型后，应使用类型和规格适合的吊兜。
如果患者/被照护人不满足这些条件，应使用其他设
备/系统产品。
预计使用寿命
担架式吊兜/一次性担架式吊兜的预计使用寿命为
最长有效使用期。
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：开裂、弯曲、断裂）。如
果看到任何此类损坏情况，请勿使用吊兜。
担架式吊兜/一次性担架式吊兜的预计使用寿命：
使用时间：
• 2 年（担架式吊兜）
• 一次性吊兜：2 周（基于每天转运 4 次）（一次
性担架式吊兜）
保质期：
• 5 年（担架式吊兜/一次性担架式吊兜）
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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，切勿清洗一次性吊兜。一次性吊
兜仅限“一名患者使用”。
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，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。
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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 第18 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。
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（7 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16 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. 检查吊兜、吊架和移位机的允许组合，请参阅
第19 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。
3. 检查吊兜的所有部件，请参阅
第18 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
• 断线
• 裂口
• 破洞
• 布料染污
• 连接环扣损坏
• 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。
4. 检查吊兜是否干净。如果吊兜不干净，请参阅
第24 页的“清洁和消毒” 。
5. 务必检查一次性吊兜标牌上的洗涤标志。如果一
次性吊兜已被清洗，请将一次性吊兜丢弃。请参
阅 第24 页的“一次性吊兜 – 请勿清洗” 。
6. 如果出现此标志，请勿使用一次性吊兜。
标牌表明一次性吊兜已被清洗。
7. 使用吊兜之前，请阅读移位机 IFU 以了解有关转
运、运输和淋浴的信息。
每次使用后
如果患者出院，应丢弃该患者专用的一次性吊兜。
1. 吊兜标牌（位于吊兜外部）
2. “不可洗涤”标牌（仅在一次性担架式吊兜上，位
于吊兜外部）
3. 带环吊带
4. 如厕孔（仅限某些吊兜）
5. 脚端
6. 首端
吊兜示例。未示出所有型号。
34
5
1
2
6
1
3
5
6
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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。
通过测量患者的头部和脚部来选择 担架式吊兜 。确保选择适合的规格以避免患者脚部从吊兜上垂落。
转运/如厕
料号 安全承重 产品说明 规格
MAA1151 272kg(600lbs) 环扣担架式吊兜 L（1610毫 米 ），XL（1650毫米）
MAA1150 272kg(600lbs) 带如厕孔的环扣担架式吊兜 L（1610毫 米 ），XL（1650毫米）
MFA5000 272kg(600lbs) 一次性环扣担架式吊兜 一种尺寸（1740 毫米）
淋浴
料号 安全承重 产品说明 规格
MAA1152 272kg(600lbs) 带如厕孔的沐浴用环扣担架式
吊兜 L（1610毫 米 ），XL（1650毫米）
允许组合
警告
为避免人身伤害，请始终遵循本 IFU 中所列的允许组合。不允许进行其他组合。
安全承重 (SWL)
始终遵守总体系统的最低 SWL。例 如 ，Maxi Move 移位机的 SWL 为160 kg (352 lbs)，MAA1151 吊兜的
SWL 为272 kg (599 lbs)。这意味着 Maxi Move 移位机 具有最低 SWL。患者体重不得超过最低 SWL。
移位机 Maxi Move MaxiSky600 Maxi Sky 2
安全工作载荷
(SWL) 160kg(352lbs) 272kg(600lbs) 272kg(600lbs)
吊架 担架吊架 700-19302 担架吊架 700-19522 担架吊架700-15695
吊兜 安全工作载荷
(SWL) 规格 规格 规格
MAA1150 272kg(600lbs) L、XL L、XL L、XL
MAA1151 272kg(600lbs) L、XL L、XL L、XL
MAA1152 272kg(600lbs) L、XL L、XL L、XL
MFA5000 272kg(600lbs) 一种规格 一种规格 一种规格
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应用吊兜
在床上（21 个步骤）
1. 将移位机放在附近。
2. 应用床制动并在可能时将床高调整到符合人体
工程学的位置。
3. 患者需要仰卧平躺。
4. 沿中线纵向折叠吊兜，外部朝外。吊兜标牌位于
外部。
警告
为避免侧翻过程中出现人身伤害，确保有另一位
护理员在场和/或在另一侧使用床栏。
5. 将患者侧翻。（使用当地技术。）如果无法侧翻，请
使用 Arjo 床单式移位易/套管放置吊兜。请参阅
相关
床单式移位易/套管 IFU。
6. 将折叠的吊兜放在患者侧部上方。
7. 向下折叠吊兜顶部并塞到患者身下。如果使用
担架式如厕吊兜，则确保如厕孔的位置正确。
（请见图 4）
8. 将患者侧翻到另一侧。
9. 将吊兜剩余部分从患者身体下方抽出。
10. 将患者恢复为仰卧体位。
11. 确保：（请见图 5）
• 吊兜居中、平直且无褶皱。
• 吊兜的头端覆盖患者头部；
• 吊兜部位未在患者下方扭曲；以及
• 如果使用担架式如厕吊兜，则确保如厕孔的
位置正确
警告
为避免人身伤害，确保患者手臂放在吊兜内。
继续执行下一页的步骤。
连接与拆除环扣
连接环扣（5 个步骤）
1. 将连接环扣放在弹簧锁 (A) 上方。（请见图 1）
2. 下拉连接环扣迫使锁打开。
3. 确保弹簧锁完全闭合且连接环扣位于其中。
（请见图 1）
4. 确保该锁可灵活移动。
5. 确保环与吊带未扭曲。
提示
使用更短的环扣长度以减少吊兜摆动。
拆除环扣（2 个步骤）
拆除环扣之前，确保接收面可承受患者体重。
方法 1
1. 按下弹簧锁以打开。
2. 取出环扣。
方法 2
1. 将连接环扣的一侧放在挂钩和弹簧锁上方。
（请见图 2）
2. 下拉环扣（请见图 3）
图
1
A
图
2
图
3
图
4
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