Dräger Babytherm 8004 User manual

WARNING
For a full understanding of the perform-
ance characteristics of this medical
device, the user should carefully read
these Instructions for Use before use of
the medical device.
Babytherm®8004/8010
Open Intensive Care, Resuscitation
Instructions for Use

2
Definitions
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 equipment or other property.
NOTE
A NOTE provides additional information intended to avoid
inconvenience during operation.

Contents
3
Contents
Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
For Your Safety and that of Your Patients . . . . . . . . . . . 4
General WARNINGS and CAUTIONS . . . . . . . . . . . . . . . . 5
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Operating Concept . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Use of accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Recommended measures for increasing stability . . . . . 9
Maximum loading . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Shelf . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Compact rail/rail brackets . . . . . . . . . . . . . . . . . . . . . . . . . 11
Swivel tray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Ensuring stability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
X-ray tray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Warming bed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Fitting the panels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Fitting the inner panels . . . . . . . . . . . . . . . . . . . . . . . . 13
Mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Tilting the bed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Bed canopy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Bronchial aspirator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Fastening the ejector on the compact rail . . . . . . . . . . 15
If the ejector is mounted on the bed . . . . . . . . . . . . . . 15
Accessories for oxygen therapy . . . . . . . . . . . . . . . . . . . . 16
O2flowmeter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Nebuliser . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
O2distributor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
O2monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
O2supply via injector . . . . . . . . . . . . . . . . . . . . . . . . . 16
Fitting the hose bracket . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Drainage canister hook . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Compressed air distributor/socket strip . . . . . . . . . . . . . . 17
Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
In-hospital transport . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Testing Readiness for Operation . . . . . . . . . . . . . . . . . 18
Before using for the first time . . . . . . . . . . . . . . . . . . . . . . 18
Scale-Tronix®4002-BT . . . . . . . . . . . . . . . . . . . . . . . . 18
Before each use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Checking height adjustment (optional) . . . . . . . . . . . . 19
Switching on and activating the self-test . . . . . . . . . . . 19
Checking LEDs, displays and audible alarm . . . . . . . . 20
Testing the power failure alarm . . . . . . . . . . . . . . . . . . 20
Testing the lights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Testing phototherapy (optional) . . . . . . . . . . . . . . . . . 20
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Switching on . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Manual operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
15 minutes alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Using baby control mode . . . . . . . . . . . . . . . . . . . . . . . . . 25
ThermoMonitoring . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Using heated gel mattress . . . . . . . . . . . . . . . . . . . . . . . . 31
Using the bed canopy . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Recommended heater settings for heat therapy . . . . . . . 37
Using phototherapy (optional) . . . . . . . . . . . . . . . . . . . . . 40
Switching lighting On/Off . . . . . . . . . . . . . . . . . . . . . . . . . 42
Central alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
Configuration mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Oxygen therapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Bronchial aspiration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Taking X-rays . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Using Scale-Tronix®4002-BT . . . . . . . . . . . . . . . . . . . . . 50
Weighing with zero calibration . . . . . . . . . . . . . . . . . . 51
Weighing without zero calibration . . . . . . . . . . . . . . . . 52
Shutting down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Dismantling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Disinfecting/cleaning/sterilising . . . . . . . . . . . . . . . . . . . . . 53
Before next use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
General system failures . . . . . . . . . . . . . . . . . . . . . . . . . . 55
System faults – Babytherm 8010 (Mattress heating) . . . . 55
System faults - radiant warmer . . . . . . . . . . . . . . . . . . . . . 56
System faults - Scale-Tronix®4002-BT . . . . . . . . . . . . . . 57
Maintenance Intervals . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Disposing of the unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
What’s What . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Complete unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Radiant warmer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Controller . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Controller, rear view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64
Scale-Tronix®4002-BT . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Technical Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Scale-Tronix®4002-BT . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
Construction and Description . . . . . . . . . . . . . . . . . . . . 72
Alarm description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Scale-Tronix®4002-BT . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
Order List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Parts list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77

For Your Safety and that of Your Patients
4
For Your Safety and that of Your
Patients
Strictly follow these Instructions for Use
Maintenance
Accessories
Not for use in areas of explosion hazard
Safe connection with other electrical equipment
WARNING
Strictly follow these Instructions for Use.
Any use of the product requires full understanding and
strict observation of all portions of these instructions.
The device is only to be used for the purpose specified
under "Intended Use" on page 6 and in conjunction with
appropriate patient monitoring. Observe all WARNING
and CAUTION statements throughout this manual and
all statements on device labels.
WARNING
The device must be inspected and serviced regularly by
trained service personnel.
Repair of the device may also only be carried out by
trained service personnel.
Dräger recommends that a service contract be obtained
with DrägerService and that all repairs also be carried
out by them. Dräger recommends that only authentic
Dräger repair parts be used for maintenance.
Otherwise the correct functioning of the device may be
compromised.
See chapter "Maintenance Intervals".
WARNING
Only the accessories indicated on the order list have
been tested and approved to be used with the device.
Accordingly it is strongly recommended that only these
accessories be used in conjunction with the specific
device.
Otherwise the correct functioning of the device may be
compromised.
WARNING
This apparatus is neither approved nor certified for use
in areas where combustible or explosive gas mixtures
are likely to occur.
WARNING
Electrical connections to equipment which is not listed
in these Instructions for Use should only be made fol-
lowing consultation with the respective manufacturers.
Patient safety
The design of the equipment, the accompanying literature,
and the labeling on the equipment take into consideration that
the purchase and use of the equipment are restricted to
trained professionals, and that certain inherent characteristics
of the equipment are known to the trained operator.
Instructions, WARNINGS, and CAUTION statements are lim-
ited, therefore, largely to the specifics of the Dräger design.
This publication excludes references to various hazards
which are obvious to a medical professional and operator of
this equipment, to the consequences of product misuse, and
to potentially adverse effects in patients with abnormal condi-
tions.
Product modification or misuse can be dangerous.
Patient monitoring
The operators of the system must recognize their responsibil-
ity for choosing appropriate safety monitoring that supplies
adequate information on equipment performance and patient
condition.
Patient safety may be achieved through a wide variety of dif-
ferent means ranging from electronic surveillance of equip-
ment performance and patient condition to simple, direct
observation of clinical signs.
The responsibility for the selection of the best level of patient
monitoring lies solely with the equipment operator.
Dräger Medical GmbH

For Your Safety and that of Your Patients
5
General WARNINGS and CAUTIONS
The following WARNINGS and CAUTIONS apply to general
operation of the device. WARNINGS and CAUTIONS specific
to subsystems or particular features appear with those topics
in later sections of the manual.
Note on EMC/ESD risk for the device function
General information on electromagnetic compatibility (EMC)
pursuant to international EMC standard IEC 60601-1-2: 2001
Electromedical devices are subject to special precautionary
measures concerning electromagnetic compatibility (EMC)
and must be installed and put into operation in accordance
with the EMC information included in the technical documen-
tation which is available from DrägerService on request.
Portable and mobile RF communications equipment can
affect medical electrical equipment.
WARNING
Connector pins with an ESD warning sign
should not be touched and no connections
should be made between these connectors
without implementing ESD protective measures. Such
precautionary procedures may include antistatic cloth-
ing and shoes, the touch of a ground stud before and
during connecting the pins or the use of electrically iso-
lating and antistatic gloves. All staff involved in the
above shall receive instruction in these ESD precau-
tionary procedures.
CAUTION
It is the responsibility of the appropriate clinical decision-
maker to draw conclusions from the skin temperature meas-
urements taken.
WARNING
Baby control mode must not be used with children who
are in shock or who have fever.
WARNING
Only use the integrated scale to determine the weight of
the patient.
Failure to follow the Instructions for Use 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 exter-
nal scale.

Intended Use
6
Intended Use
Babytherm 8004/8010 is an open care unit for warming pre-
mature babies, neonates and infants with a body weight of up
to 8 kg.
The unit may be used in operating theatres, neonatal wards,
children’s wards, obstetric units and paediatric intensive care
units. The unit may be operated by clinical staff or by nursing
staff under the supervision of a doctor.
Therapy and nursing uses
– In intensive care and obstetric units for resuscitation, nor-
mal and intensive care
– For infant warming and compensation of heat loss
– Thermal stability with mattress heating
– Gentle heat therapy with a combination of radiant warmer
and mattress heating
– Cooling patients with fever (temperature of mattress below
core temperature)
– Adjustable bed angle for head-up or head-down position
– Weaning infants from incubators
–O
2and nebuliser therapy (with appropriate accessories)
– Lowering the bilirubin levels when using the phototherapy
option.
Babytherm 8004 heating features
– Radiant warmer operation with a preset heat output:
the radiant warmer output is set in manual mode, and ther-
apy time at the higher heater output level is monitored.
– Radiant warmer operation with baby control mode:
temperature is automatically monitored and controlled.
Babytherm 8010 heating features
– Radiant warmer operation with a preset heat output:
the radiant warmer output is set in manual mode, and ther-
apy time at the higher heater output levels is monitored.
– Radiant warmer operation with baby control mode: tem-
perature is automatically monitored and controlled.
– Heated gel mattress, operating independently of the radi-
ant warmer:
the temperature of the heating pads is automatically mon-
itored and adjusted to attain and maintain a preselected
temperature at the contact surface between the infant and
the mattress.
Options
– Height adjustment
– One or two swivel cabinets
– Side panels (150 mm or 230 mm)
– Infusion holder
– Phototherapy
– Bed canopy
–Swiveltray
– RS 232 interface
Optional therapy accessories
– Bronchial aspirator
–O
2flowmeter
–O
2distributor
–O
2distributor with cylinder connection
–O2monitor
–O
2hood
Scale-Tronix®4002-BT
is an integrated scale for the Babytherm 8004/8010.
It is designed to determine the weight of the patient with the
bed in a horizontal or inclined position.
MEDIBUS
Software protocol for the transfer of data between
Babytherm 8004/8010 and an external medical or non-medi-
cal device (e. g. patient monitors or computers for data man-
agement systems) via an RS 232 port, see "MEDIBUS for
Dräger Pediatric Devices" (9029205).
All transferred data are for information only and should not be
used as basis for diagnostic or therapeutic decisions.
To protect the patient and the user against electrical hazards,
it is essential that all systems consisting of medical devices
as well as other electrical devices which are not restricted to
computers, printers etc., are only assembled by trained per-
sonnel.
The system must meet the requirements of the
IEC/EN 60601-1-1 and IEC/EN 60601-1-2 standards.

Intended Use
7
000
20 15 10 5 0 5 10 15 20
Babytherm 8004 Babytherm 8010
Check
Inop.
Babytherm 8004
OK
1
5
10
°C
skin
man.
skin °C manual
D
Check
Inop.
Babytherm 8010
OK
1
5
10
>38 °C
<36 °C
°C °C
skin
man.
skin °C manual matress °C
D

Operating Concept
8
Operating Concept
➀ON/OFF indicator:
The green LED is lit when the unit is ON.
The red LED is lit following a power failure.
➁OK button for confirming advisory messages and settings.
If the OK button is not pressed within 10 seconds of enter-
ing a new setting, the previous settings remain active.
➂"Inop." alarm display.
➃Pushbutton for checking the LEDs, displays, siren and
audible alarm.
➄Pushbutton for switching off the audible alarm.
➅Visual display for alarms:
Warning = red LED. Caution = yellow LED.
➆Text display: shows advisory messages for the user.
➇Babytherm 8010 only – display and keypad for the heated
gel mattress:
top: display for the measured mattress temperature;
bottom: display for the set mattress temperature,
with buttons for setting the desired temperature.
right: indicators for operation in extended setting
range – high (>38 °C) or low (<36 °C).
094
Check
Inop.
Babytherm 8010
OK
1
5
10
>
38 °C
<
36 °C
°C °C
skin
man.
skin °C manual mattress.°C
➀
➁
➂
➃
➄
➅
➆
➇
➈
➉
➈Display and keypad for the radiant warmer:
top: display for the measured value of the core and periph-
eral skin temperature;
bottom: display for the set skin temperature, with buttons
for setting the desired value and a toggle button for select-
ing "man." (manual mode) or "skin" (baby control mode).
The active mode is indicated by the relevant yellow LED;
right: display of heater levels 1 to 10, for manual operation
of the radiant warmer:
Heater levels 1 to 3 = green LEDs
Heater levels 4 to 10 = yellow LEDs
complete with buttons for selecting the desired increment.
➉On/Off buttons for:
Procedure light,
Night light,
Phototherapy, optional,
Radiant warmer.
Each of these buttons has a yellow LED that is lit when
the relevant function is switched on.

Preparation
9
Preparation
Use of accessories
1 Stand column
2Shelf
3 Base plate
4 Swivel cabinet
5Compactrail
6 Standard rail
Recommended measures for increasing stability
Attach accessory loads as low and as close to the stand
columns as possible and avoid one-sided loading.
To ensure stability**, observe the following restrictions
when using accessories:
– Do not exceed a maximum patient weight of 8 kg
– Observe a maximum weight limit of 20 kg for the shelf and
a maximum mounting height of 40 cm above the base
plate
– Maximum loading of 2.4 kg for a swivel cabinet,
corresponding to a maximum total weight of 9 kg
– Mount swivel cabinets (2M20638) on opposite sides, if
present.
WARNING
Stability may be impaired by the attachment of
additional accessories/loads. In order to ensure
stability (EN 60601-2-21), a one-sided accessory load of
25 Nm* must not be exceeded, when tilted at 10°.
* corresponds to approx. 5 kg at a distance of 20 cm from the
stand column, at a height of 2.00 m when tilted at 10°
** EN IEC 60601-2-21 tilt stability ensured up to an inclination of
10°
108
Observe maximum
loading
44
6
5
3
2
1

Preparation
10
When attaching one-sided stand column accessories
without swivel cabinets
Maximum permissible one-sided accessory load on the stand
column:
– 4 kg at a height of 200 cm and at a distance of 20 cm
When attaching swivel cabinets and stand column
accessories on the same side
For one-sided mounting of the swivel cabinet (2M20638)
Maximum permissible one-sided accessory load on the stand
column:
– 1 kg at a height of 200 cm and at a distance of 20 cm
or
– 2 kg at a height of 130 cm and at a distance of 10 cm
Example:
1.5 kg (approx. 1 L of infusion liquid including bracket) at a
distance of 20 cm from the stand column, at a height of
180 cm corresponds to a tilting moment of approx. 7 Nm
(at an inclination of 10°).
For opposite/diagonal mounting of swivel cabinets
(2M20638)
Maximum permissible one-sided accessory load on the stand
column:
– 2.5 kg at a height of 200 cm and at a distance of 20 cm
or
– 4.5 kg at a height of 130 cm and at a distance of 10 cm
For same-sided mounting of swivel cabinets (2M20638)
Maximum loading of 2.4 kg = maximum total weight of 9 kg
per cabinet
– No one-sided accessory load on the stand column
– Maximum loading of the shelf (2M21158) restricted to
2.5 kg
Maximum loading
Lifting columns/standard
housing
<50 kg
of which
Weight of patient <8.0 kg
Swivel cabinet <2.4 kg Observe diagonal
mounting position
Shelf <20 kg Observe maximum
mounting height of
140 cm
Stand column <5.0 kg Attach accessory loads
as low and as close to the
stand columns as
possible and avoid one-
sided loading
Maximum tilting moment <25 Nm
Individual wheel load <100 kg

Preparation
11
Shelf
The unit is fitted with one shelf.
Make sure that the shelf is firmly in position.
To fit rails to the shelf:
1Screw rail to the left and/or right of the shelf.
●Place desired auxiliary equipment on the rails and shelf.
Max. 20 kg per shelf.
2Fasten infusion holder to stand column at the required
height.
Compact rail/rail brackets
This rail is designed to hold auxiliary equipment,
e.g. O2flowmeter, O2monitor, infusion pumps.
3Fasten the compact rail(s) to one column of the stand at
the required height.
4Fasten rail brackets and
5small equipment bar to one column of the stand at the
required height.
Swivel tray
For small articles and parts. Max. load 3 kg.
●Position the swivel tray on one of the columns of the stand
and tighten the hand screw.
Recommended height: level with the mattress.
●Make sure that the swivel path is kept clear of obstructions!
Ensuring stability
Stability is ensured when the unit is placed on a surface
with a slope of not more than 10°.
The following restrictions apply when adding accessories:
●Do not exceed the maximum load-bearing capacity of
the stand = 30 kg.
●If accessories are positioned on a column of the stand,
e.g. on two swivel trays, the maximum load for this col-
umn is 5kg.
003
1
2
004
3
3
4
4
5
005

Preparation
12
X-ray tray
Babytherm 8004 only
Preparation
1Push X-ray tray fully home in the horizontal position.
2Lower X-ray tank into the bed
– the pegs engage in the holes in the X-ray tank.
●Prepare the warming bed, see page 13.
NOTE
Do not use the X-ray tray in the extended position to rest on
while writing. Do not place objects other than X-ray plate.
Do not lean on the tray.
Risk of damage.
006
1
007
2
2

Preparation
13
Warming bed
The bed is enclosed by two side panels and two end panels
that can be opened independently of one another.
The side panels are provided with holes for secretion and
drainage hoses.
The end panels have flexible grommets for hoses and cables.
Fitting the panels
1Insert the lower mounting pins of the panel hinge-pieces
into the guide slots on either side.
With the panels on the long side, ensure that the handle
points outwards.
●Position the panel semi-upright,
2press the panel down firmly until the pins lock into position
at the bottom of the slots.
●Fold the panel up into the vertical position and allow it to
drop into the locking position.
●Fit all four panels in this way.
Make sure that the panels are seated correctly.
To open:
●Lift the panel all the way up until the upper pins come out
of their slots, then fold the panel down.
With lively infants or older children:
●Use 230 mm high panels.
Fitting the inner panels
●Insert the pins into the tapered holes in the corners of the
housing and press down lightly until the inner panel is
firmly in place.
Make sure the panels are seated correctly.
Mattress
●Lay gel mattress flat in the cot and cover it with a cotton
sheet.
●Lay SoftBed in the warming therapy device dimpled side
up.
No additional sheet is required for the patient to lie on.
●Lay the patient on the dimpled side.
WARNING
Inner panels should be used with all patients, regard-
less of whether the side panels are up or down!
Otherwise the patient may fall out!
008
11
22
009

Preparation
14
Tilting the bed
1Pull the handle of the locking mechanism out towards
the front.
2Press handle down = head-up position.
Pull handle up = head-down position.
●Release the handle: the bed automatically locks into the
selected position.
The bed can be tilted in finely graduated steps.
Maximum tilt angle:
Head-up position: 20°
Head-down position: 15°
Preferred positions:
Horizontal,
10° tilt head-up and
10° tilt head-down.
The mattress may slip at maximum tilt.
In this case do not place a sheet over the mattress.
Bed canopy
Optional
Higher side panels (230 mm) are recommended when using
the canopy.
●Check that the bed canopy is closed.
When the bed canopy is not required:
●Attach bracket to standard rail.
3Hang bed canopy from bracket.
010
1
095
2
011012
3

Preparation
15
Bronchial aspirator
Fastening the ejector on the compact rail
●Fit the compact rail to the desired position on the stand,
see page 11.
1Clip the ejector to the compact rail.
2Mount bracket with projecting support to one of the posi-
tions provided on the column.
For units with height adjustment, place the bracket so that
the bottle holder is outside the path of the swivel cabinet.
3Place the bottle holder on the projecting support.
4Connect hoses.
●Fit the hose clip (optional) to the compact rail.
5Clip aspiration hose into the hose clip.
●Screw on the connecting hose and plug the connector into
the socket of the central supply system (park position).
If the ejector is mounted on the bed
●Mount bracket with projecting support to one of the posi-
tions provided on the column.
For units with height adjustment, place the bracket so that
the bottle holder is outside the path of the swivel cabinet.
●Place the bottle holder on the projecting support.
●Fasten hose clip to frame.
6Connect hoses.
7Clip aspiration hose into the hose clip.
●Screw on the connecting hose and plug the connector into
the socket of the central supply system (park position).
●Prepare the aspirator in accordance with its specific
Instructions for Use.
013
1
3
5
2
4
014
6
7

Preparation
16
Accessories for oxygen therapy
O2flowmeter
●Prepare the flowmeter in accordance with its specific
Instructions for Use.
To mount the flowmeter on the compact rail:
1Press the slider all the way down; hook the flowmeter to
the compact rail and release the slider.
2Screw on the O2connecting hose.
3Insert the connector of the connecting hose into the O2
delivery socket and press it all the way in.
Nebuliser
●Prepare the nebuliser in conformity with its specific Instruc-
tions for Use.
4Screw the nebuliser securely to the flowmeter.
5Fit the spiral hose to the nebuliser port.
O2distributor
Different versions are available for connection either to a
pipeline system or an oxygen cylinder.
●Hang the O2distributor from the standard rail.
●Connect the O2supply.
●Connect the O2load.
O2monitor
e.g. MiniOx 3000
●Prepare the O2monitor in conformity with its specific
Instructions for Use.
●Fasten O2monitor, complete with its holder, to the com-
pact rail.
●Place the O2sensor on the bed and feed the cable through
the hole on the front.
●Plug the connector of the sensor into the measuring unit.
O2supply via injector
When using the injector, the higher side panels (230 mm) and
the bed canopy should be used (pages 13 onwards).
6Press locking lever on mounting flange and push injector
into flange.
●Allow locking lever on injector to engage. The injector is
now locked.
●Connect up hose.
O2supply should only be used with O2concentration
monitoring, e.g. via MiniOx 3000.
015
3
1
45
2
016017018
6

Preparation
17
Fitting the hose bracket
●Insert the hose bracket into the hole in the left side of the
head panel and tighten with knurled screw.
Drainage canister hook
1Insert hook horizontally into hole in the Babytherm casing.
2Pivot hook downwards.
Compressed air distributor/socket strip
●Secure the compressed air distributor to the standard rail.
●Secure the socket strip to the standard rail.
Storage
Units with height-adjustable column:
– One or two swivel cabinets each with 2 swivel compart-
ments and 1 swivel tray, optional.
Units without height adjustment:
– Two open compartments in the column
– One swivel cabinet with two swivel compartments and one
swivel tray, optional.
●For clearly organised storage of required equipment and
accessories.
In-hospital transport
●Monitor the patient’s core temperature.
●If optional height adjustment is fitted, lower the unit to its
lowest position.
●Swivel the swivel cabinets inwards.
●Swivel the swivel tray inwards.
●Remove X-ray cartridge from X-ray tray (see page 49).
●Accessories projecting beyond either side of the unit must
be removed or folded in.
●Switch off heating systems and disconnect the mains plug.
●Fit optional bed canopy to protect patient from draughts.
Immediately after transport:
●Plug in the mains plug and switch on the heating systems.
019098
1
22
020

Testing Readiness for Operation
18
Testing Readiness for Operation
Before using for the first time
1Check that the mains voltage matches the values indicated
on the rating plate next to the power cable.
2Plug into the mains.
Scale-Tronix®4002-BT
Before using the scale:
●Loosen the locking screws (4x) under the bed by about
1cm.
Before transporting Babytherm:
●Tighten the locking screws (4x) under the bed.
Before each use
●Check that the unit has been disinfected.
●Check that the side panels are locked securely into place.
The panel hardware must be visible above the bed sur-
face.
●Check that the side panels are free from cracks and sharp
edges.
●Check that the correct mattress is in the cot;
Operation with mattress heater: gel mattress
Operation without mattress heater: foam mattress.
●Check that the bed tilts properly and locks securely into
position.
●Check that the required accessories and therapy equip-
ment are available and in proper working order.
●Check that the gas supply is available and sufficient for the
accessories and equipment to be used.
●Check that the cables and hoses are correctly and
securely installed. Never route cables or hoses over the
panels because they might be pinched or crushed when
folding up the panels or fitting the bed canopy.
●Check whether both infrared radiators are providing
warmth by placing your hand carefully at a safe distance
from the radiant heater.
NOTE
To safeguard during transport, the weighing unit inside
Babytherm has been protected against vibration and shock.
To ensure correct operation, this protection must be
removed before using the scale.
021
2
1
105

Testing Readiness for Operation
19
Checking height adjustment (optional)
Test height adjustment system if fitted:
1Press the right pedal briefly to raise the bed.
2Press the left pedal briefly to lower the bed.
●Remember the maximum load for height adjustment is
50 kg.
●Hoses and cables should be long enough to ensure a
secure connection even in the top or bottom height adjust-
ment position.
●Do not place any objects in the raising/lowering path.
●Adjust to a comfortable working height.
Switching on and activating the self-test
●Press the On/Off button until it engages = ON.
Babytherm now runs a self-test to check important func-
tions.
3The following message appears in the display:
»All displays on, horn on«.
All the displays are lit for about 2 seconds: digital displays
read »88.8« and a continuous tone sounds.
3The following message appears in the display:
»All displays off, soft alarm on«.
All displays are dark for about 2 seconds and the alarm
sounds.
4The green LED is lit.
5After about 2 seconds, the unit displays the radiant warmer
mode:
»man.« (manual mode) – no skin temperature sensor in
place
or
»skin« (baby control mode) – yellow skin temperature
sensor for core temperature in place.
The corresponding LED flashes.
6The preset desired values are displayed.
3If the text display reads »Battery charge low«
7and the yellow LED is lit, the battery is being charged for
the power failure alarm. It takes about 30 minutes to
charge the battery.
7The yellow LED is extinguished.
8If the red LED »Inop.«= operating fault is lit,
see page 55.
022
12
023
024
15 min
Babytherm 8010
1
5
10
<36 C
C
skin
man.
skin C manual mattress. C
5
66
3
7
4
8

Testing Readiness for Operation
20
Checking LEDs, displays and audible alarm
1Press the key.
2The following message appears in the display:
»All displays on, horn on«.
All the displays are lit for about 2 seconds:
digital displays read »88.8« and a continuous tone sounds.
2The following message appears in the display:
»All displays off, soft alarm on«.
All displays are dark for about 2 seconds and the alarm
sounds. A function check can also be carried out while the
unit is in operation.
●Check at least once a day.
Testing the power failure alarm
●Disconnect the power plug.
3The red LED should light up and a continuous alarm
tone should sound.
●Reconnect the power. The unit will continue to operate
with the values set before the power failure alarm.
Testing the lights
4Press the left-hand button. The bed should now be illumi-
nated by the procedure light.
4Press the button again. The procedure light will be
switched off.
5Press the middle button. The bed should now be lit by the
night light.
5Press the button again. The night light will be switched off.
Testing phototherapy (optional)
6Press button. The yellow LED in the button will start to
flash.
8The following message appears in the text display:
»Phototherapy: Use eye protection
Press OK button to start XX:XX:XX«.
7Press OK button = phototherapy lights switched on.
8The following message appears in the text display for
5 seconds:
»Duration of phototherapy XX:XX:XX«.
6The yellow LED in the button is now continuously lit.
6Press button.
8The following message appears in the text display:
»Phototherapy turned OFF
Press OK button to confirm XX:XX:XX«.
7Press OK button = phototherapy switched off.
6The yellow LED in the button will go out.
025
15 min
Babytherm 8010
1
5
10
<36 C
C
skin
man.
skin C manual mattress. C
2
1
Check
026
15 min
Babytherm 8010
1
5
10
<36 C
C
skin
man.
skin C manual mattress. C
3
456
8
7