Caleo Neonatal Incubator Sw 2.n Instructions for Use 2nd Edition 9 Jan 2015.pdf
Page 1
Caleo®
WARNING
To properly use this medical device, read and comply
with these Instructions for Use.
Neonatal incubator
Software 2.n
Instructions for Use
Page 2
How to use the Instructions for Use
How to use the Instructions for Use
The headline...
specifies the subject of the main chapter.
for fast orientation and navigation.
Preparation
Before using for the first time
Mounting accessories
Preparation
The left-hand column...
contains text
The text provides explanations and instructs the user step-bystep in the practical use of the product, with short, clear instructions in easy-to-follow sequence.
z Dots refer to actions.
1 Numbers refer to the illustrations next to the text and to the
sequence of actions in the case of operations consisting of
several steps.
Before using for the first time
Check that all packaging materials have been completely
removed (see packing slip in the pack).
Check that the mains power supply voltage matches the
voltage rating specified on the nameplate (see page 140).
z Check that the height above sea level is correctly set
(see page 83).
z
z
Mounting accessories
CAUTION
When fitting accessories, please note
Any mounted accessories should not collide with the unit
when adjusting the tilt angle and heigh oft Caleo®. Risk of
damage. Install the accessories such that a collision with the
device is ruled out.
Screw
NOTE on pole 38 mm/600 (2M 50 691) or
When fitting accessories, please note:
Accessories mounted on the handle side do not move
with the main unit during the height adjustment of Caleo®
(see page 123). Hoses or cables can be stretched during the
height adjustment of Caleo. Lay hoses or cables such that
they are sufficiently long during the height adjustment.
Screw on pole 38 mm/600 (2M50691) or
pole 38 mm/310 (2M 50 688) or
pole 25 mm/600 (2M 50 689).
z Remove the cover plate from the base frame.
z Screw the pole fully into the base frame and tighten firmly.
Make sure that it is securely held in place.
228
The page...
contains instructions for use of the unit
combine text and illustrations. The information is translated
directly into practical actions showing the user how to use
the unit.
Observe the maximum loads.
Danger of overturning the unit!
Pole 38 mm/600
10 kg
Pole 38 mm/310
10 kg
Pole 25 mm/600
3 kg
Distance between the loads and the pole: max. 150 mm
Moving the control unit to the opposite side
for pole, 38 mm
1 Remove the control unit = loosen the clamping screw.
2 Remove the holder = loosen the clamping screw.
On delivery, the control unit is fixed to the 38 mm/310 tube.
This tube is secured by a screwed fixing for transport. If
required, the tube can be released (recommendation: ask for
assistance from specialized technical personnel):
3 Remove both caps from the tube. Insert a screwdriver in the
holes and release the tube.
To fit the control unit to the adjacent side:
Push the holder over the tube and set it to the desired
working height.
2 Mount the bracket = tighten the clamping screw.
z Set the control unit to the desired working height.
1 Secure the control unit to the holder = tighten the clamping
screw.
WARNING
A WARNING statement provides important information
about a potentially hazardous situation which, if not
avoided, could result in death or serious injury.
CAUTION
A CAUTION statement provides important information about
a potentially hazardous situation which, if not avoided, may
result in minor or moderate injury to the user or patient or in
damage to the medical device or other property.
NOTE
A NOTE provides additional information intended to avoid inconvenience during operation.
2
2
3
024
z
14
Safety Information Definition
1
147
The right-hand column...
contains illustrations
The illustration shows the relationship to the text and the orientation to the device. The elements mentioned in the text are
highlighted, and unnecessarydetails are omitted. The user is
guided by screens confirming the various steps required for
each action.
Page 3
Table of contents
Table of contents
For Your Safety and that of Your Patients
4
Intended Use
6
What's what
8
Preparation
14
Check readiness for operation
32
Operation
40
Cleaning, disinfecting and sterilizing
94
Maintenance intervals
106
Disposal
109
Message – Cause – Remedy
112
Error – Cause – Remedy
118
Technical Data
120
Description
126
Order List
143
Parts List
146
Index
147
3
Page 4
For Your Safety and that of Your Patients
Definition of target groups
Definition of target groups
Users, maintenance personnel and professionals are defined
as the target groups for this medicine device.
These target groups were trained to handle the medical device
and have the necessary specialized knowledge and training,
the necessary know how to use, install, prepare, maintain or
repair the medical device.
Dräger points out that only the defined target groups should
use, install, prepare, maintain or repair the medical device.
User
Users are persons who may use the medical device in accordance with its intended purpose.
Maintenance personnel
Maintenance personnel are persons who are responsible to the
owner or operator for the maintenance of the medical device.
Maintenance personnel are persons who install, prepare or
maintain the medical device in working condition.
Professionals
Professionals are persons who may perform repair jobs or
complex maintenance jobs on the medical device.
For Your Safety and that of Your
Patients
General Safety Information
The following WARNING and CAUTION statements apply to
general operation of the medical device.
WARNING and CAUTION statements specific to subsystems
or particular features of the medical device appear in the
respective sections of these Instructions for Use or in the
Instructions for Use of another product being used with this
device.
Strictly follow these Instructions for Use
WARNING
Any use of the medical device requires full understanding and strict observation of all sections of these
Instructions for Use. The medical device may be used
only for the purpose specified on page 6 under "Intended
use" in connection with a suitable patient monitoring
system (see page 5). Strictly observe all WARNING and
CAUTION statements throughout these Instructions for
Use and all statements on medical device labels. Failure
to observe these safety information statements constitutes a use of the medical device that is inconsistent with
its intended use.
Maintenance
WARNING
The medical device must be inspected and serviced regularly by professionals who possess the required qualifications due to their training and their experience. Repair of the medical device must also be performed by
trained personnel with additional product-specific
DrägerService training.
Dräger recommends that a service contract is obtained
with DrägerService and that all repairs are performed by
DrägerService. Dräger further recommends that only authentic Dräger repair parts are used for maintenance.
If the above are not complied with, the correct functioning of the medical device may be compromised.
See chapter "Maintenance".
Safety checks
The medical device must be subject to regular safety checks.
See chapter "Maintenance".
Accessories
WARNING
Only the accessories mentioned in the order list have
been tested and approved for use with the medical
device.
Therefore, it is strongly recommended that only these
accessories are used in conjunction with the medical
device. Otherwise, the correct functioning of the medical
device may be compromised.
Connected devices
WARNING
Risk of electric shock and of device malfunction
Any connected devices or device combinations not
complying with the requirements mentioned in these
Instructions for Use may compromise the correct functioning of the medical device. Before operating any
combination of devices, refer to and strictly comply with
the Instructions for Use for all connected devices and
device combinations.
Not for use in areas of explosion hazard
WARNING
This medical device is neither approved nor certified for
use in areas where combustible or explosive gas
mixtures are likely to occur.
Safe connection with other electrical equipment
CAUTION
Risk of patient injury
Electrical connections to equipment not listed in these
Instructions for Use or these Assembly Instructions must only
be made when approved by each respective manufacturer.
4
Page 5
For Your Safety and that of Your Patients
Definition of target groups
Connection to other devices
Device combinations approved by Dräger (see Instructions for
Use of the individual devices) meet the requirements of the
following standards:
– IEC 60601-1 (EN 60601-1st, 2nd Edition)
Medical electrical equipment
Part 1: General requirements for safety
– IEC 60601-1-1 (EN 60601-1-1)
Medical electrical equipment
Part 1-1: General requirements for safety
Collateral standard: Safety requirements for medical
electrical systems
– IEC 60601-1-2 (EN 60601-1-2)
Medical electrical equipment
Part 1-2: General requirements for safety
Collateral standard: Electromagnetic compatibility;
Requirements and tests
– IEC 60601-1-4 (EN 60601-1-4)
Medical electrical equipment
Part 1-4: General requirements for safety
Collateral standard: Programmable electrical medical
systems
If Dräger devices are connected to other Dräger devices or
third-party devices and the resulting combination is not
approved by Dräger, the correct functioning of the devices may
be compromised. The owner is responsible for ensuring that
the resulting system meets the requirements of the applicable
standards.
Strictly observe Assembly Instructions and Instructions for Use
for each networked device.
Patient safety
The design of the medical device, the accompanying documentation, and the labeling on the medical device are based
on the assumption that the purchase and the use of the
medical device are restricted to professionals, and that certain
inherent characteristics of the medical device are known to the
user. Instructions and WARNING and CAUTION statements
are therefore largely limited to the specifics of the Dräger
medical device.
These Instructions for Use do not contain references to various
hazards which are obvious to professionals who operate this
medical device as well as references to the consequences of
medical device misuse, and to potentially adverse effects in
patients with different underlying diseases. Medical device
modification or misuse can be dangerous.
CAUTION
Risk of patient injury.
Do not make therapeutic decisions based solely on individual
measured values and monitoring parameters.
Patient monitoring
The user of the medical device is responsible for choosing suitable monitoring that provides appropriate information about
medical device performance and the patient's condition.
Patient safety may be achieved by a wide variety of means
ranging from electronic surveillance of medical device performance and patient condition to simple, direct observation of
clinical signs.
The responsibility for selecting the best level of patient monitoring lies solely with the user of the medical device.
Functional safety
The essential performance characteristics consist of a
controlled and monitored air-conditioning of the incubator interior with user-defined settings for the monitoring functions.
– Air temperature
– Relative humidity
– O2 enrichment (optional)
or, if a set limit is exceeded, an appropriate alarm. The medical
device is equipped with basic safety features to reduce the
possibility of patient injury while the cause of an alarm is remedied.
Information on Electromagnetic Compatibility
General information on electromagnetic compatibility (EMC)
according to international EMC standard IEC 60601-1-2:
Medical electrical equipment is subject to special precautionary
measures concerning electromagcompatibility (EMC) and must
be installed and put into operation in accordance with the EMC
information provided on page 139.
Portable and mobile RF communications equipment can affect
medical electrical equipment.
WARNING
Do not connect connectors with an ESD warning
symbol and do not touch the pins of such
connectors without implementing ESD protective measures. Such protective measures may include
antistatic clothing and shoes, touching a ground stud
before and during connection of the pins, or using electrically insulating and antistatic gloves. All relevant
personnel must be instructed in these ESD protective
measures.
WARNING
Do not use skin temperature control on children who are
in a state of shock, or have fever! Skin temperature is
considerably higher than usual. The control function
would overcool the incubator, resulting in the risk of
hypothermia.
WARNING
Only use the integrated scale to determine the weight of
the patient.
Failure to follow the Operating Instructions can lead to
severe inaccuracies in measuring the patient’s weight.
To safeguard critical therapeutic decisions based on the
patient’s weight, the weighing result should be checked
against a reference measurement on an external scale.
5
Page 6
Intended Use
Intended Use
Therapy system for premature babies and sick neonates up to
a body weight of 5 kg or a body length of 55 cm, for the
controlled supply of warmth, humidity* and O2 enrichment* in
the patient capsule.
For the therapy of twins, the total body weight is limited to 5 kg.
Locations of use
Clinical environment in which premature babies or neonatesrequire controlled climate parameters.
The device may only be used by properly trained personnel
under the supervision of qualified medical personnel familiar
with the currently known risks and benefits of using an
incubator.
Therapy and care options
–
–
–
–
–
Heat therapy through air temperature control or skin
temperature control
Humidification
O2-Therapy through controlled O2 enrichment
Normal and intensive care via access ports or a large
front flap
Bed with pivoting adjustment for raising and lowering
the head
With Monitoring for
–
–
–
–
–
Air temperature
Skin temperature
Relative humidity
O2 concentration
weight*
*
optional equipment feature
6
Page 7
What's what
What's what
What's what . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Front view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Side view, connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Top view, bed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Connections on the back of the Control Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
8
8
9
9
Operating concept . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Control panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
7
Page 8
What's what
What's what
Front view
1
2
3
4
5
6
7
8
9
10
11
12
13
14
Canopy (2M 51 108)
Access ports
Front flap
Handle for transport
Housing
Drawer (2M 50 565)*
Pedals for height adjustment*
Height adjustable pillar*/Housing support
Connection for water heater (LuerLock)
X-ray drawer/removable bed
Screen
Control panel
Pillar element
Double wall* (2M 51 150)
14
12 13
11
1
2
3
4
10
9
5
6
8
24
Side view, connections
15
16
17
18
19
20
21
22
23
24
25
26
27
Central alarm indicator
Sensor unit, temperature connections
Mains power connection
On/off switch
Fresh air filter flap
Connection for O2 control*
Water container (2M 50 040)*
Tubing grommet (2M 50 385)
Side flap
Tubing grommet (2M 50 412)
Feeding grommet plug (2M 51 109)
Trolley castor with direction lock
Trolley castors with brakes
25
111
7 7
15
16
23
22
17
18
21
19
*
8
optional equipment feature
27
26
27 27
112
20
Page 9
What's what
Top view, bed
1
2
Spirit levels
Hot air duct
1
1
2
223
1
2
Connections* on the back of the Control Unit
3
4
5
Nurse call
MEDIBUS*
Service RSB (Remote Service Box)
284
3
4
5
*
optional equipment feature
9
Page 10
Operating concept
Operating concept
Control panel
these permanently defined keys enable the user to select
various functions of Caleo®:
1 Scale*
2 Bed tilt
3 Menu selection/configuration
4 Changeover key: air/skin temperature control
5 Trend display
6 Suppress alarm tone
7 Lock key pad function
8 Rotary knob
12 13 14 15
3 4 5
9
10
6
Menu
7
Air
Skin
8
Visual signals indicate alarm situations
9 Red bar LED**
10 Yellow bar LED***
11 Power failure alarm
Soft Keys
These keys, with variable functions defined by different labels
on the screen, guide the user through the specific routines of
the unit, from preparing for use to shutting down the unit.
Depending on the current menu, different soft keys with varying
functions and labels are activated. Only the soft keys required
for the current menu actually appear. This precaution keeps
the display clear, preventing any confusion for the user.
When a soft key is pressed, its function is activated and the
relevant menu is displayed on the screen.
In the standard screen, the soft key labels are as follows:
12 Air/skin temperature
13 Humidity*
14 O2*
15 Day and Night
* Optional equipment feature
** Warning – immediate action is required
*** Caution – rapid action is required
10
1
2
11
040
Hard Keys
Page 11
Operating concept
Rotary knob
A single rotary knob is used to select and set parameters.
Turn knob = select
Press knob = confirm
D
193
z
z
Screen
By default, the measured values are displayed as numeric
values (standard screen).
–
–
–
–
–
Set values and actual measured
values for air temperature/skin temperature
Set values and actual measured values for relative
humidity*
Set values and actual measured values for
O2 concentration*
Day and Night (to adjust the brightness of the screen)
Alarms and warnings
000
The screen display can also include a trend graph.
*
optional equipment feature
11
Page 12
12
Page 13
Preparation
Preparation
Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Before using for the first time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Mounting accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Doors, ports and bed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Check readiness for operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Before First-time Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Before Every Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
13
Page 14
Preparation
Before using for the first time
Mounting accessories
Preparation
Before using for the first time
Check that all packaging materials have been completely
removed (see packing slip in the pack).
z Check that the mains power supply voltage matches the
voltage rating specified on the nameplate (see page 140).
z Check that the height above sea level is correctly set
(see page 83).
z
Mounting accessories
CAUTION
When fitting accessories, please note
Any mounted accessories should not collide with the unit
when adjusting the tilt angle and heigh oft Caleo®. Risk of
damage. Install the accessories such that a collision with the
device is ruled out.
NOTE
When fitting accessories, please note:
Accessories mounted on the handle side do not move
with the main unit during the height adjustment of Caleo®
(see page 123). Hoses or cables can be stretched during the
height adjustment of Caleo. Lay hoses or cables such that
they are sufficiently long during the height adjustment.
228
Screw on pole 38 mm/600 (2M50691) or
pole 38 mm/310 (2M 50 688) or
pole 25 mm/600 (2M 50 689).
z Remove the cover plate from the base frame.
z Screw the pole fully into the base frame and tighten firmly.
Make sure that it is securely held in place.
Observe the maximum loads.
Danger of overturning the unit!
Pole 38 mm/600
10 kg
Pole 38 mm/310
10 kg
Pole 25 mm/600
3 kg
Distance between the loads and the pole: max. 150 mm.
Moving the control unit to the opposite side
for pole, 38 mm
1 Remove the control unit = loosen the clamping screw.
2 Remove the holder = loosen the clamping screw.
On delivery, the control unit is fixed to the 38 mm/310 tube.
This tube is secured by a screwed fixing for transport. If
required, the tube can be released (recommendation: ask for
assistance from specialized technical personnel):
3 Remove both caps from the tube. Insert a screwdriver in the
holes and release the tube.
To fit the control unit to the adjacent side:
Push the holder over the tube and set it to the desired
working height.
2 Mount the bracket = tighten the clamping screw.
z Set the control unit to the desired working height.
1 Secure the control unit to the holder = tighten the clamping
screw.
1
2
3
14
024
z
Page 15
Preparation
Mounting accessories
NOTE
Contol unit without space for free swivel movement.
Risk of damage to control unit.
Make sure there is sufficient space to swivel the unit.
WARNING
Mounting the control unit on the handle side.
Only specialized technical personnel may move the
control unit from the wall side to the handle side or vice
versa.
Else there is danger of wrong installation and therefore,
risk of injury to the user.
To install the basic pole (2M 50 680), see page 16.
Screw in the extension pole 38/600 (2M 50 691) or
pole 38/310 (2M 50 688).
z Refit the control unit as specified in the Assembly
Instructions.
z
z
256
CAUTION
The cable to the control unit must not be removed from
the cable guides on the basic pole. Risk of damage.
Without sufficient swivelling space, the cable may get
damaged.
Make sure there is sufficient space to swivel and tilt the unit.
Infusion support (2M 21 514)
for pole, 38 mm
Max. load per hook 3 kg
Push the fixing claw onto the stand pillar.
Push the infusion holder into the fixing and secure it firmly
with the clamping screw.
010
z
z
Swivel table (2M 21 186)
for pole, 38 mm
For small parts, max. load 3 kg
z Place the clamp of the swivel table on the stand pillar and
tighten the clamping screw.
020
CAUTION
Without sufficient swivelling space, the cable may get
damaged.
Make sure there is sufficient space to swivel and tilt the unit.
15
Page 16
Preparation
Mounting accessories
Compact rail (2M 85 337)
for pole, 38 mm
Max. load 5 kg.
WARNING
Only specialized technical personnel should perform the
installation, else there is risk of incorrect installation and
therefore, risk of injury to the user.
For fixing accessories, e.g.
– O2 monitor
1
2
Adjust the height of the compact rail to the required height
of the mounted accessory.
Fit the compact rail to the pole = push the compact rail over
the pole and
fasten with the screws.
Bronchial aspiration system (2M 85 125)
2
1
101
z
Follow the separate Instructions for Use of the bronchial
aspirator.
Fix the bronchial aspirator holder to the standard rail on the
wall side or handle side.
z Tighten the clamping lever.
z Establish the hose connections.
230
z
Basic pole (2M 50 680)
Maximum load 10 kg
WARNING
Only specialized technical personnel should perform the
installation, else there is risk of incorrect installation and
therefore, risk of injury to the user.
z
Mount as specified in the Assembly Instructions.
Distance between the loads and the pole: max. 150 mm
16
019
For fixing accessories, e.g.
– For additional pole extensions, see page 17.
– Swivel table (2M 21 186), see page 15.
– Monitor support plate (2M 50 085), see page 18.
Page 17
Preparation
Mounting accessories
Shelf 3020 (M 24 678)
Maximum load must not exceed 2 kg!
Hang the shelf from the standard rail on the wall or handle
side and secure in position.
021
z
Pole extensions
The following poles can be fixed to the base pole as extensions:
– Pole 38 mm/600 (2M 50 691) or
– Pole 38 mm/310 (2M 50 688) or
– Pole 25 mm/600 (2M 50 689).
z
Screw the pole into the base pole as far as it will go and
tighten securely. Make sure that it is securely held in place.
229
Observe the maximum loads:
Pole 38 mm/600
5 kg
Pole 38 mm/310
5 kg
Pole 25 mm/600
3 kg
Distance between the loads and the pole: max. 150 mm
17
Page 18
Preparation
Mounting accessories
Monitor shelf (2M 50 085)
The monitor shelf can be mounted on the wall side and/or the
handle side.
Maximum load must not exceed 20 kg!
Shelf for monitor and ventilation equipment.
WARNING
Only professionals should perform the installation, else
there is risk of incorrect installation and therefore, risk of
injury to the user.
To mount the monitor support plate,
– on the wall side, use a second pole 38 mm (see page 14),
– on the handle side, use a second base pole (see page 16)
with a pole extension 38 mm (see page 16).
1
Mount as specified in the Installation Instructions.
Fit the monitor shelf = slide the shelf over both 38 mm poles
and
fix in place with the screws.
max. 20 cm
1
1
023
CAUTION
The vertical stability can be affected if the shelf is placed too
high. Threat to patient or user.
To obtain safe veritical stability, observe maximum installation
height.
max. 100 cm
z
z
Hose holder for ventilation hoses (84 11 075)
Open the front flap.
Raise the bed and pull it out of the incubator.
Push the mattress slightly to one side.
Place the hose holder in the mounting hole in the bed and
fasten from underneath with the locking screw.
z Replace the bed in the incubator and close the front flap.
z
z
z
z
The hose holder can be fixed to any of the four corners of
the bed.
2
Clip the ventilation hoses and cables into the clips at the end
of the ventilation hose holder.
2
008
2
18
Page 19
Preparation
Mounting accessories
O2 enrichment with O2 control*
1
Screw the O2 connection hose to the underside of the
incubator.
NOTE
In case of a loose O2 connection hose a leakage in the
compressed gas inlet occurs, supply pressure in the device is
too low.
Check the hose for tight connection.
1
Insert the probe into the outlet of the central O2 supply
pipeline and place it in the "Park" position (see the
associated Instructions for Use).
The permissible gas pressure is between 300 and
600 kPa.
011
z
O2 monitor
Monitoring the O2 concentration with the help of an O2 monitor
with alarm limits:
z Fix the O2 monitor to the compact rail using the holder.
z Place the sensor capsule in Caleo®.
z Route the sensor cable through one of the flexible tubing
grommets. Where applicable, push the sensor plug into the
socket of the O2 monitor (e.g. Oxydig or MiniOx 3000) until
it audibly clicks into place (see separate Instructions for Use
of O2 monitor).
2
213
The contour of the vacuum mattress can be altered as required
and is then maintained after air evacuation of the mattress.
Extreme positions can therefore be obtained for special applications. The mattress can remain in the incubator.
z Open the front flap.
z Insert and preform the vacuum mattress.
z Place the patient on the mattress and adjust the mattress to
the desired shape.
z Connect the vacuum mattress to the hose of the suction
system.
2 Open the valve and evacuate the vacuum mattress.
2 Close the valve and disconnect the hose.
z Close the front flap.
028
Vacuum mattress (2M 17 909)
Fitting the drawer (2M 50 565)
Maximum load must not exceed 7 kg.
z
Mount as specified in the Installation Instructions.
Fit the drawer = slide the drawer box into the groove in the
base frame.
*
optional equipment feature
z
118
WARNING
Only specialized technical personnel should perform the
installation, else there is risk of incorrect installation and
therefore, risk of injury to the user.
19
Page 20
Preparation
Doors, ports and bed
Doors, ports and bed
Access ports
To open the access port:
1 Press down the knurled area of the locking bolt. The access
port opens.
1
1
014
To close the access port:
z Press the access port closed until the locking bolt engages.
Front flap
To open the front flap:
2 Turn the two knobs inwards to the vertical position.
The red latch becomes visible.
2
015
2
z
Lower the front flap until it hangs down vertically towards
the floor.
Take care not to trap hoses and cables in the moveable double
wall of the front flap!
To close the front flap:
Raise the front flap and press into position,
3 Turn the two locking knobs outwards to the horizontal
position until you feel them click into place.
WARNING
Danger of excessive cooling or overheating of the
patient. If the moveable double wall is not parallel to the
front flap, the hot air duct is interrupted.
The moveable double wall must be positioned parallel
to the front flap. Align the moveable double wall if necessary!
20
3
3
091
WARNING
Flap can open on its own, danger to patients.
Make sure that both locking knobs are engaged. The red
latches must no longer be visible.
016
z
Page 21
Preparation
Doors, ports and bed
Side flap
The side flap is opened and closed the same way as the
front flap (see page 20).
231
z
Double wall*
The double wall (2M 51 150) can only be fastened to the
canopy (2M 51 108).
1
270
Fitting the double wall
1 Pull the plunger up as far as it will go.
The red shaft of the plunger will then be visible.
z Place the double wall on the hood.
2
3
Position the centering lugs in the recesses in the hood.
Place the bore sleeve of the double wall assembly in the
hole for the "feeding grommet" plug.
z Lay the contour seal (gasket) of the double wall evenly on
the hood.
2
3
271
2
Securing the double wall
4 Push the plunger down into the sleeve until it engages.
The red shaft of the plunger must no longer be visible.
*
282
4
optional equipment feature
21
Page 22
Preparation
Doors, ports and bed
1
2
2
272
Removing the double wall
1 Pull the plunger up as far as it will go.
The red shaft of the plunger will then be visible.
2 Grip the double wall with both hands and lift it off.
Storing the double wall
z Fix the hanger (2M 51 152) to the compact rail of the Caleo.
3 Hook the double wall by its plunger to the hanger.
3
273
CAUTION
If Caleo is lowered too far, the double wall may touch the
floor. Risk of damage.
Observe the set height of the Caleo.
Make sure that if the Caleo is lowered the double wall does
not touch the floor.
Canopy
To open the canopy:
4 Grasp the handle of the canopy
and
5 open it (approx. 60o).
4
104
WARNING
Danger of overturning the canopy.
Do not tilt the canopy over the side. Tip the canopy only
longitudinally, as shown.
5
Raise the side canopy prop, and lower the canopy until the
prop is fixed in the slot in the canopy.
To close the canopy:
4 Grasp the handle on the canopy and raise it slightly.
6 Fold down the prop
and
z close the canopy.
The canopy can be opened from both sides.
22
6
196
6
Page 23
Preparation
Doors, ports and bed
To remove the canopy:
1 Hold the canopy with both hands using the handles on
the side.
2 Lift the canopy horizontally off the pillar elements.
To replace the canopy:
2 Replace the canopy horizontally, so that the guide pins fit
into the holes in the pillar element.
1
1
2
2
093
NOTE
Take care of the sensor unit, risk of damage.
Removing the bed
Maximum load must not exceed 5 kg
z
Open the front flap and fold it down.
Pull the bed out:
3 Turn both knobs to the vertical position marked
,
4 Grasp the bed by the recessed handle or by the knobs and
pull it out towards the front as far as it will go.
WARNING
Patient can fall out! Danger to the patient.
When the bed is pulled out, the patient must be monitored constantly to prevent the risk of a fall.
3
4
3
z
187
CAUTION
The bed can be damaged when leaning on it, maximum
load 5 kg.
Do not lean or rest any weight on the bed when it is
pulled out.
After carrying out the care operations, push the bed back
until it clicks into place. Turn the knobs to the horizontal
position marked
, and close the front flap.
WARNING
If the bed is not fully pushed in, danger of interruption of
the hot air duct. The result may be excessive cooling or
overheating of the patient.
Slide the bed in fully.
23
Page 24
Preparation
Doors, ports and bed
Using the X-ray drawer
The X-ray drawer can be pulled out when the front flap is either
open or closed.
To open the X-ray drawer:
1 Turn both knobs to the horizontal position marked
,
2 pull the drawer out by the recessed handle or the knobs.
z Insert or remove the X-ray cassette. Recesses are provided
in the X-ray drawer for positioning.
To close the X-ray drawer:
2 push the drawer inwards under the bed until it tangibly clicks
into place.
2
1
1
017
NOTE
Do not use the pulled-out X-ray drawer as writing support or
bed for the patient. Do not store anything on the drawer!
Risk of injury to patient or damage.
Do not lean on the drawer.
WARNING
If the X-ray drawer is not fully pushed in, danger of interruption of the hot air duct. The result may be excessive
cooling or overheating of the patient.
Slide the X-ray drawer in fully.
Grommets
3
4
5
6
Tubing grommet (2M 50 412)
Tubing grommet (2M 50 412) for high-frequency ventilation*
Hose modules (2M 50 385)
The feeding grommet plug (2M 51 109) can only be used if
no double wall is attached to the canopy.
z
Route the cables or hoses through the flexible tubing
grommets
3
5
5
4
095
The hose holder for vetilation hoses is provided to route ventilation hoses and cables through Caleo® (page 18).
6
Hose fixing devices*
285
The hose fixing devices (2M 51 140) can only be attached to
hose modules with pins (2M 51 139). Hose fixing devices act
as guides for hoses and cables.
*
24
optional equipment feature
Page 25
Preparation
Doors, ports and bed
Drainage module*
The drainage module (2M 51 142) can only be mounted onto
the pillar elements (2M 51 154 and 2M 51 156).
The drainage module facilitates the installation of hoses for
patient drainage.
Open the side flap.
Positioning the hoses in the drainage module.
z Close the side flap.
z
1
1
275
CAUTION
Hoses that are not routed correctly and safely without
obstruction can kink, tear or become squashed!
Ensure that all hoses are routed correctly and safely without
obstruction.
Drawer (2M 50 565)
Drawer for storing items required for nursing or treatment.
The drawer is accessible from both sides.
Open the drawer:
2 grasp the drawer by the handle and pull it out as far as it
will go.
z
Place the required material in the drawer.
2
013
Close the drawer:
2 push the drawer back in by the handle.
*
optional equipment feature
25