This Product will perform in conformity with the description thereof
contained in this operating manual and accompanying labels and/orinserts, when assembled, operated, maintained and repaired in accor-dance with the instructions provided. This Product must be checkedperiodically. A defective Product should not be used. Parts that arebroken, missing, plainly worn, distorted or contaminated should bereplaced immediately. Should such repair or replacement become neces-sary, Ohmeda recommends that a telephone or written request forservice advice be made to the nearest Ohmeda Regional Service Center.This Product or any of its parts should not be repaired other than inaccordance with written instructions provided by Ohmeda and byOhmeda trained personnel. The Product must not be altered without theprior written approval of Ohmeda’s Quality Assurance Department. Theuser of this Product shall have the sole responsibility for any malfunctionwhich results from improper use, faulty maintenance, improper repair,damage, or alteration by anyone other than Ohmeda.
!
A
CAUTION: Federal law in U.S.A. and Canada restricts this device tosale by or on the order of a licensed medical practitioner.
All models of the Ohmeda Infant Warmer System provide a controlled
source of radiant heat for infants and pediatric patients. The control sys-tem uses a microprocessor and provides both manual and servo modes ofoperation (except for the 2001 International, which is manual mode only).
The model 2001 International has an integral infant bed and is a manualmode only warmer designed for short term attended care in the OR andL&D.
The wall mounted 3050, 3100 and 3150 models are available to accommo-date specific architectural requirements in the NICU, L&D, LDR and LDRProom
.
The 3050 is a heater head only, the 3100 is a heater and dove tail
rails, and the 3150 includes a heater, rails and integral bed.The model 3300 has an integral bed for infants and is intended for proce-
dures and long term care in the Nursery and L&D.The model 3000, 3500 and 4000 are free standing Warmers which can be
used over a variety of infant bassinets in the general nursery, over post-operative patients, during patient feeding, and in any other applicationwhere controlled radiant heat is required.
The 3500 System also has a detachable Bassinet for infants, and is in-
tended for procedures and long term care in the Nursery, L&D, LDR and
LDRP Rooms.The model
4300,440O
and 5000 have a larger size bed than the model 3300and are intended for surgical procedures and long term care in the Nurseryand L&D Rooms. Both the 5000 and 4400 have an elevating pedestal toraise and lower the bed-to-floor height. The model 4400 has a narrower
foot print than the 5000 warmer. The model 4300 is a non-elevatingversion of the 4400.
IWS Model Options
Large Heater/Bed
4000
5000
Series Series4000
Free StandingWall mounted,
heater head onlyWall mounted heater
with rails
Wall mounted heaterwith rails and bad
Standard Heater/Bed20003000
3500
Series Series Series
3000
3500t
3050
3100
3150
vi
Free standing withintegral bed
Elevating pedestal
t Detachable bassinet and wood
6600-0194-000
11109/93
grain
2001
finish standard.
3300
430044005000
AWarnings
Operator Safety
Before using the Ohmeda Infant Warmer System, read this entiremanual. Attempting to use this device without a thorough understand-ing of its operation may result in patient or user injury. This deviceshould only be operated by personnel trained in its operation and underthe direction of qualified medical personnel familiar with the risks andbenefits of this type of device.
Overloading the shelves can affect the stability of the unit. Limit the loadto 20 lbs. (9 kg) per instrument shelf, mounted to a single upright, and
50 lbs. (23 kg) per monitor shelf, mounted between the uprights.
Limit the load of accessories to 50 pounds (23 kg) per side on the Warmer
to ensure stability. Accessories should not be mounted more than
56 inches (142 cm) above the floor. For models 3000 and 3500, limit theload of accessories to 20 pounds (9 kg) maximum per side mounted no
more than 44 inches (112 cm) above the floor.Limit the load placed on the x-ray cassette tray to 5 lbs (2.2 kg) to avoid a
tipping hazard.
Overloading the drawers can affect the stability of the unit. Limit the load
to 10 lbs. (4.6 kg) per drawer.Do not use the Warmer in the presence of flammable anesthetics; a
possible explosion hazard exists under these conditions.Do not touch the protective grill under the radiant heater or the top of the
heater assembly. These surfaces may be hot and a burn could result.Due to the increased height of units with the ECMO option installed, a
tipping hazard may exist if tip loading occurs. Limit the total accessoryload to 50 lbs. (23 kg), no more than 25 lbs (11 kg) per side.
Use caution when rotating the cabinet to avoid damage to the drawers orpossible injury. Always ensure the drawers are fully closed before rotatingthe cabinet.
Disconnect power to the Warmer and allow the heater rod to cool before
cleaning to avoid the possibility of a burn.
Never oil or grease oxygen equipment. Oils and grease oxidize readily,and in the presence of oxygen, will burn violently. Vat-Kote is the onlyoxygen service lubricant recommended (Ohmeda Stock No. 6700-0092-
200) if the use of a lubricant is specified.Disconnect the Warmer power cord and allow the unit to cool before
replacing the alarm or observation lights.On elevating models, check for proper clearance above the Warmer and
below the bed surface before raising or lowering the bed.Enclosing the heater assembly inside a cabinet may prevent proper
ventilation and may create a fire hazard. If the heater is enclosed in acabinet, it must be equipped with a power cut-off device that preventsoperation while the cabinet is closed.
6600-0194-000
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ix
Precautions
Keep hands clear of the hinge area when installing a wall mountedheater assembly. A pinch hazard exists.
The 3050 heater assembly weighs approximately 30 lbs (14 kg). Properinstallation may require two people. Due to the weight of the 3100 and3150 units, approximately 75 lbs. (34 kg), proper installation will requiretwo people.
Patient Safety
f
Bed-to-heater spacing which differs from the specified 27
(69
&
5 cm)will result in incorrect operation and may affect the patient’s
condition.
Do not place any accessories or any other objects directly over the bed
surface. This may block radiant heat and lead to cooling of the infant.
Do not place items on top of the heater assembly. Items placed on top ofthe heater assembly can fall and injure the patient, prevent adequateventilation of the heater assembly, and may pose a fire hazard.
Do not perform the Checkout Procedures (Mechanical and Control Unit)while a patient occupies the Warmer.
2 inches
Complete the “Checkout Procedures” section of this manual beforeputting the unit into operation. If the warmer fails any portion of thecheckout procedures it must be removed from use and repaired.
Regularly inspect the bed side panel latching mechanism, and the bed-side locking mechanism on the model 3500, to ensure proper operation.
In the service position the strength of the wall mounted unit hingebracket is reduced. Never place a patient in the bed when the heater is inthe service position. Never leave the unit unattended in the serviceposition or with a pin removed.
Check for proper clearance above the Warmer and below the bed surfacebefore raising or lowering the bed.
Inspect all patient connected tubes or wires before and after moving ortilting the bed. Tilting or moving the warmer bed up or down can pull ontubing or leads connected to the patient. This may disconnect tubes orleads, restrict gas or liquid flow, or move sensors out of position.
Prolonged exposure to the light emitted by the observation lamp in thisunit may harm the unprotected eyes of the infant. For safety, cover theinfant’s eyes.
Do not use the Warmer system if the system failure alarm is activated.Remove the unit from service and refer to qualified personnel for repair.
Radiant energy can adversely affect blood components. When usingintravenous tubing systems for delivery of blood components to patientsoccupying a warmer, shield any tubing with aluminum foil.
When using a radiant warmer, change the patient’s diapers frequently.
Radiant energy causes more rapid urine evaporation, and may lead to
inaccurate urine diagnostic test/ analysis and inaccurate weight mea-
surements.
X
*1109/936600-0194.000
Precautions
Do not install chest drainage tubes in the Tubing Organizer Rear SidePanel.
Install tubing in the appropriately sized holes. Use of inappropriate holes
may cause kinking, pinching or restriction of flow through the tubes, andmay interfere with the proper operation of therapy equipment.
Do not lower the Tubing Organizer Rear Side Panel with tubing attached.
Lowering can pull on the tubing, causing the tubes to dislodge from the
patient.
Do not move the warmer by pushing or pulling on the bed side panels.
This action may lead to the deterioration and breakage of the compo-
nents which form a safety barrier around the infant.
Ensure that the bedside panels are locked in position when a patient
occupies the bed. Blankets or other foreign objects may prevent the
latches from fully engaging.Do not leave the patient unattended when the side panels are lowered.Never place an infant on the X-ray cassette tray.
Do not place any foreign objects on the warmer bed or in the under bedcavity while performing X-ray procedures. Incompatible materials in thepath of the X-ray may adversely affect the quality of the X-ray image. Useof mattress or bedding materials other than those supplied by Ohmedashould be evaluated by a Neonatologist or Radiologist.
Do not leave the patient unattended when using the warmer. Check thepatient’s temperature regularly to ensure the comfort and the safety ofthe patient. If the warmer is used for an extended time, it is recom-mended that the servo mode of operation be used. When an alarm issilenced, close monitoring of the patient’s condition is required.
Use the servo mode unless the manual mode is specifically prescribed.
While both modes require patient monitoring, the manual mode requiresconstant attention. In the manual mode, you must take the
for detecting changes in the environment (drafts, direct sunlight, therapy lamp usage, etc.) or the patient condition requiring heater
adjustments in response to these changes. In the servo mode, the infant
warmer automatically adjusts heater output to maintain the desired skintemperature, reducing (but not eliminating) the need to monitor thepatient and make adjustments to the equipment.
Use of electrosurgical units or other electrical field radiating equipmentcan affect the operation of the warmer. Keep the patient probe lead as faraway as possible from electrosurgical cables. Do not allow excess electri-cal cables to be laid on the bed platform. Use of electrosurgical units orother instruments which radiate electrical fields can cause indirectheating, by several tenths of a degree of the skin temperature probe dueto absorbed electrical energy. When using these devices near the radiantwarmer, operate the Infant Warmer in manual mode for maximum safety.
The use of phototherapy equipment may raise the patient’s temperature.
responsibihty
photo-
Radiant warmers increase an infant’s insensible water loss. Take appro-priate measures to maintain the patient’s fluid balance while caring forthem in a radiant warmer.
Use only the Reusable Ohmeda skin temperature probe (Stock No. 0208-
0697-700) and heat reflective patches (Stock No. 0203-1980-300,
6600-0194-000
11/09/93
50/pkg)
xi
Precautions
or the disposable probe (Stock No. 6600-0208-700,
6600-0196-700. other manufacturer’s probes may affect the accuracy of warmer opera-tion and the electrical safety of the patient.
The skin temperature probe should be located on the patient’s skin in anarea which is directly in the path of the radiant heat. It should not beattached to an area which is shielded from the radiant heat or betweenthe patient and the mattress. Large temperature gradients and very longservo response times will result from improper probe placement.
Rectal temperatures must never be used to servo control a patient’stemperature.
Intimate contact between the skin temperature probe tip and thepatient’s skin must be maintained for accurate skin temperature mea-surement. Underheating or overheating may result from poor contactbetween the skin temperature probe and the patient. Verify that the skintemperature probe is securely attached to the patient at least once everyhalf hour.
In the servo mode, verify that the patient temperature probe is securelyattached to the patient at least once every half hour. A dislodged probemay not trigger an alarm. If the probe becomes dislodged, the warmercan over or under heat the infant.
50/pkg)
to monitor the patient’s skin temperature. Use of
lO/pkg;
Stock No.
Oxygen concentrations higher than 40% can increase the risk of tal fibroplasia (retinopathy or prematurity). It is probable that evenconcentrations of 40% or less oxygen (formerly considered safe) could bedangerous to some infants. Therefore, arterial blood gas measurementsare extremely important for regulation of the concentration of inspiredoxygen when an oxygen-enriched environment is considered necessary.(See current edition of “Standards and Recommendations for HospitalCare of Newborn Infants” prepared by the Committee of Fetus andNewborn of the Academy of Pediatrics.)
Do not leave both cylinder valves open. Leaving both oxygen cylindervalves open at the same cylinders with no reserve oxygen supply available.
Use only one cylinder gasket per yoke. Use of more than one gasket could
cause leakage of the cylinder gas
Do not leave gas cylinder valves open if the pipeline supply is in use.Pressures from both oxygen cylinders may become equal, and if simulta-neously used, cylinder supplies may be depleted, leaving no reservesupply in case of pipeline failure.
The patient probe is not isolated from earth ground. Any additionalequipment used with the Ohmeda Infant Warmer System must complywith UL 544, CSA 22.2, IEC 601 and VDE 750.
time will allow simultaneous depletion of both
retrolen-
Xii
The computer or RS-232 monitor’s user program must continuously checkthe data link. The program should constantly verify connection to thewarmer controller and check for updated data.
Remote monitoring does not replace the need for direct patient
6600-0194-000
11109/93
observa-
Precautions
ACautions
tion by qualified medical personnel.If you connect the Nurse Call output to a system which uses a normally
open connection, a disconnected Nurse Call cable will not trigger analarm.
When installing a wall mounted unit, to achieve adequate structuralstrength all four holes of each mounting bracket must engage tracks.Should the hole saw miss a track do not proceed. Consult the projectengineer for further direction.
To prevent the drawers from opening unintentionally while moving the
3500 Bassinet, move it from the front only.
On elevating models, do not continue to run the motor at the upper and
lower limit positions; equipment damage may result.
Yoke check valves are not intended to provide a leak-free seal; always
use a yoke plug and a fresh cylinder gasket to seal an unused cylinder
port.
Open cylinder valves S-L-O-W-L-Y to avoid damaging the regulators.
Use cleaning solution sparingly on a cloth when cleaning the Warmer. Do
not saturate the unit
components.Use of cleaning/disinfecting solutions containing chemicals that are not
listed in the table on page 4-2 (i.e. alcohol, acetone, etc.), or chemicals in
greater concentrations than those listed, may damage the patient probe
or other material being cleaned.Do not autoclave or gas sterilize the skin temperature probe. Do not
immerse the probe in liquid cleaner. Avoid placing excessive strain onthe probe lead. Always remove the probe by grasping the plug at thepanel. Do not pull on the probe lead. These precautions will help avoiddamage to the probe.
Do not autoclave or gas sterilize the mattress.
Only competent individuals trained in the repair of this equipment shouldattempt to service it as detailed in the service manual. The ServiceManual provides detailed information solely for use by individuals havingproper knowledge, tools and test equipment, and for service representa-tives trained by Ohmeda.
-
excessive solution causes damage to internal
6600-0194-000
11/09/93
. .
Xlll
In this section
1.1 General
1.1
General l-l
Support Structure
1.2
Heater Assembly
1.3
Control Unit l-2
1.4
Bed Platform l-2
1.5
Bassinet (3500 Series) l-2
1.6
Accessories l-3
1.7
All models of the Ohmeda Infant Warmer System provide a controlled
source of radiant heat for infants and pediatric patients. The control
system uses a microprocessor and provides both manual and servomodes of operation (model 2001 International is manual mode only). Thepatient temperature, control temperature, and elapsed time displays aredigital for ease of viewing. The control panel includes a one hour elapsedtimer with time displayed in minutes and seconds. The timer featuresoptional audible tones for use during Apgar scoring. A complete audioand visual alarm system is included on the control panel.
l-l
l-l
The optional 232 serial data is provided for use with customized research software orcompatible vital signs monitors. The Nurse Call connection lets youintegrate the Warmer into your current or future remote alarm systems.
1.2 Support Structure
The support structure provides excellent stability for the radiant heaterand optional accessories. On free standing units, the support structureconsists of the base assembly and the uprights with an integral railsystem. The rails provide a means for mounting accessories and ancillaryequipment to the unit. Refer to Section 1.7 for a description of the acces-sory items.
1.3 Heater Assembly
The warmer is designed to warm infants on a bed surface located 27
!
A
inches
WARNING: Bed-to-heater spacing which differs from the specified 27
2 inches
patient’s condition.
For your convenience, on Model bed-to-heater spacing is indicated by a label located on the right alumi-num upright (as viewed from the front).
f
2 inches
(69+5
ThermaLink feature simplifies charting and monitoring.
(69+5
cm) beneath the heater assembly.
cm) will result in incorrect operation and may affect the
3000,3100,3500, and 4000 the proper
RS-
f
6600-0194-000
11/09/93
l-l
l/Description
The heater assembly consists of a radiant heater, parabolic reflector,observation light, and a visual alarm light. The parabolic reflector focusesradiant energy on the bed surface, minimizing energy loss due to scatter-ing and providing an even field of radiant heat over the bed surface. Theobservation light provides intense light for procedures. The alarm light islocated on the end of the heater assembly for ease of viewing. The entireheater assembly rotates to the side for X-ray procedures and for observa-tion lamp replacement.
1.4
Control Unit
The control unit contains the electronic circuits and controls used to
operate the radiant heater and the observation light. The control unitperforms regular self checks during its operation including failure diag-nostics.
Either manual or servo mode of operation may be selected. In the manualmode of operation,the % power display on the control panel. The control circuit then main-tains the selected level of radiant heat. The manual mode has a preheat
setting which allows the Warmer to be preheated. In the servo mode ofoperation, select the patient’s control temperature. A skin temperatureprobe is used to monitor the patient skin temperature. The controlsystem modulates the radiant heat to maintain the patient at the se-lected control temperature. The patient’s skin temperature is continu-ously displayed.
select the level of radiant heat output as indicated by
Alarms activate to alert the operator of a low or high patient tempera-ture, a skin temperature probe failure, a power failure, equipment failureor a check patient prompt.
1.5 Bed Platform
Warmers with beds include a mattress and transparent side panels. The
side panels fold down for easy access to the patient and can be removed
for cleaning. The X-ray cassette tray (located in an opening beneath the
bed when installed) pulls out for insertion of X-ray cassettes and allows
X-rays to be taken without moving the patient. * Markings located alongthe side panels allow easy location of the cassette in the X-ray tray
relative to the position of the patient on the warmer bed.*bed platform allows Trendelenburg and Fowler positioning. The hydrau-
lic system for the
avoid disturbing the patient. *A chest drainage hanger attached to the
bed and rear cross bar extrusion provides a convenient location to hangchest drainage devices. *
1.6 Bassinet (3500 Series)
The bassinet unit can be detached and rolled away from the model 3500
warmer unit by pulling up on the locking lever knob located at the toprear of the bassinet (see Figure l-l). The bassinet includes:
tiltable
The
tiltable bed provides a smooth, dampened motion to
l-2
1.
Transparent locking side panels which fold down for easy patient
access and are removable for cleaning.
l
Not available on the model 3500 wanner
6600-0194-000
11/09/93
l/Description
2. A mattress.
3.
4.
5. Front locking casters.
Figure l-l
Operating thebassinetlocking lever knob
A tiltable, positive-lock bed platform which allows Trendelenburg
and Fowler positioning at 4” and 8“ tilt positions Three drawers which open from the front (or from the side in an
optional configuration) for storing equipment or supplies. The top
drawer is provided with a key lock.
.
1.7 Accessories
The rail mounting system is the basis for most of the accessories for theWarmer. This patented design consists of a dovetail shaped aluminumextrusion and a positive locking mounting block. Mounting blocks are
attached to various accessories for mounting to the rail system. Themounting blocks are produced in two standard lengths and are machinedto accommodate each specific accessory.
Accessories which mount on a single upright are interchangeable be-tween all model Warmers.
Accessories can only be mounted to the inside dovetail rail on each
upright of the 3500 Warmer.
6600-0194-000
11/09/93
l-3
In this section
2.1 Setup 2-l
2.2 Mechanical Checkout Procedure 2-lA.
Overall Appearance 2-l
B.
Heater Assembly Rotation 2-2
C. Mechanical Checks 2-2
D.
Warmer/Bassinet Interlock (model 3500 only)
E.
Warmer/Bassinet Unlock (model 3500 only)
F.
Accessory Checks 2-3
G. Wall Mount Checkout 2-4
2.3 Control Unit Checkout Procedure 2-4A.
Control Unit Check 2-5
B.
Elapsed Timer Check 2-6
C.
Observation Light Check 2-6Raise and Lower Bed Switch Check (Elevating Models
D.
Only) 2-6
E.
Interlock Switch Check 2-7
F.
Power Failure, Memory and Battery Test (all models except the2001 International) 2-7
2-3
2-3
2.1 Setup
Refer to the setup instructions shipped with the warmer for initial unpack-ing and setup of the unit after shipment. For model 3050, 3100 and 3150
wall mounted units, refer to the mounting instructions in the Appendix.After removal from the shipping containers, inspect the Ohmeda Infant
Warmer System and all accessory items for any signs of damage whichmay have occurred during shipment. File a damage claim with the ship-ping carrier if damage has occurred. Also confirm the presence of allaccessory items or factory installed options as listed on the packing slip.
Mechanical Checkout Procedure
2.2
WARNING: Before using the Ohmeda Infant Warmer System, read thisentire manual. Attempting to use this device without a thorough under-standing of its operation may result in patient or user injury.
WARNING: Do not perform the Checkout Procedures (Mechanical andControl Unit) while a patient occupies the warmer.
WARNING: Complete the “Checkout Procedures” section of this manualbefore putting the unit into operation. If the warmer fails any portion ofthe checkout procedures it must be removed from use and repaired.
A
A
A
!
!
!
A.
Overall Appearance
Disconnect the power cord from the ac power source for the mechani-
1.
cal checks portion of this procedure.Check the overall appearance of the Infant Warmer/ Bassinet System.
2.There should be no obvious damage.
6600-0194-000
11/09/93
2-l
2/Setup
and Checkout Procedures
For the model 3500, separate the warmer from the bassinet.
3.For units with casters, check that all casters are in firm contact with
4.the floor and that the warmer is stable and moves freely.
For the model 3500, check that all six casters on the warmer move freely.Note: On the model 3500, it is possible that the two center casters may
not be in contact with the floor at all times.
5.
Lock the two front casters and check that the warmer is held in place.On the model 3500, lock the two rear casters and check that the
warmer is held in place.
6.
For the model 3500, place the bassinet on a level surface. Check thatall four casters are in firm contact with the floor and that the Bassinetmoves freely.
7.
For the model 3500, lock the two front casters and check that theBassinet is held in place.
8.
Examine the power cord for damage. Replace the power cord if dam-age is evident.
Examine the unit for objects placed on top of the heater assembly.
9.
!
A
!
A
!
A
WARNING: Do not place any accessories or other objects directlyover the bed surface. This may block radiant heat energy and lead tocooling of the infant.
WARNING: Do not place items on top of the heater assembly. Items
placed on top of the heater assembly can fall and injure the patient,prevent adequate ventilation of the heater assembly, and may posea fire hazard.
B. Heater Assembly Rotation
Rotate the Heater Assembly to the side and then back to the normalposition. Check for a smooth rotation.
C. Mechanical Checks
1.
Check the operation of the bed sides. The bed sides should operatesmoothly.
WARNING: Regularly inspect the bed side panel latching mecha-
nism, and the bedside locking mechanism on the model 3500, to
ensure proper operation.
2.
Check the operation of the tilt mechanism. Verify that the bed plat-form operates smoothly and locks in normal, Trendelenburg and Fowlerpositions.
!
A
2-2
3.
If the drawer package is installed, check that all the drawers open andclose freely. On units with the rotating drawer package, make sure thedrawers rotate from front to 90” left and right and firmly stop in thedetented positions.
WARNING Overloading the drawers can affect the stability of theunit. Limit the load to 10 lbs. (4.6 kg) per drawer.
4.
For the model 3500 bassinet, remove the keys from the top drawer andlock it. Check that the drawer is securely held closed.
6600-0194-000
11/09/93
2Betup
and Checkout Procedures
D. Warmer/Bassinet Interlock
Lock the 3500 warmer’s two rear casters.
1.Align the rear of the bassinet with the warmer’s base.
2.
Push the bassinet into the alignment/locking track of the warmer’s
3.
base.Continue pushing the bassinet until its locking pin drops into the
4.
socket at the end of the alignment track. There should be an audibleclick when the pin drops into position.
Lightly push and pull the bassinet to verify that the two units are
5.
securely held together.
6.
Unlock the two rear casters on the warmer and check that the com-bined unit moves smoothly.
Warmer/Bassinet Unlock
E.
1.
Verify that the two bassinet front casters are unlocked and the twowarmer rear casters are locked
With the locking pin handle (located at the rear of the bassinet)
2.
raised, pull the bassinet forward until it is fully detached from thewarmer
.
.
(model 3500 only)
(model 3500 only)
!
A
!
A
!
A
CAUTION: To prevent the drawers from opening unintentionallywhile moving the detached bassinet, move it from the front only.
Accessory Checks
F.
Perform these checks if they are applicable.
1.
Check that all accessories are mounted securely and that the loadlimits are not exceeded.
2.
Check that all gas accessories are installed and operating properly(refer to Section 3.9).
3.
Where applicable, perform the checkout procedures detailed in theOperation and Maintenance Manuals for the accessories.
the
WARNING: Limit
side
on the Warmer to ensure stability. Accessories should not be
mounted more than 56 inches (142 cm) above the floor. For models
3000 and 3500, limit the load of accessories to 20 pounds (9 kg)
maximum per side mounted no more than 44 inches (112 cm) abovethe floor.
WARNING: Due to the increased height of units with the ECMOoption installed, a tipping hazard may exist. Limit the total acces-
sory load to 50 lbs. (23 kg), no more than 25 lbs. (11 kg) per side.
load of accessories to 50 pounds (23 kg) per
6600-0194-000
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2-3
2/Setun
Figure 2-1
Wall mount pininsertion
and Checkout Procedures
G. Wall Mount Checkout
1.
Verify that the warmer is rigidly secured to the wall and the heater
assembly is level.
!
A
Note: To
procedures, either hinge pin may be removed, allowing the warmerto pivot away from the wall.
2.
Check that both hinge pins are in place and fully inserted with the
pin heads at the top of the hinge.WARNING: In the service position the strength of the hinge
bracket is reduced. Never place a patient in the bed when theheater is in the service position. Never leave the unit unattendedin the service position
access the control unit and display module for service
or with either pin removed.
2.3 Control Unit Checkout Procedure
Control
I
Figure 2-2Control Panel
BedControls
ModelPatientNumber Temperature Temperature Power % Time Display
Note: Servo mode indicator, mode switch, and probe failure international control panel. Bed
WARNING: Do not perform the Checkout Procedures (Mechanical andControl Unit) while a patient occupies the warmer.
WARNING: Complete the “Checkout Procedures” section of this manualbefore putting the unit into operation. If the warmer fails any portion ofthe checkout procedures it must be removed from use and repaired.
6600-0194-000
11/09/93
Increase
*
raise/lower
are only present on elevating models.
ApgarIndicator
alarm
ApgarTones
On/Off
are not present on the model 2001
ElapsedTimeStart/Holdand Reset
2/Setup
and Checkout Procedures
A. Control Unit Check
1.
Connect the warmer power cord to an appropriate power source.Refer to the rating plate on the Warmer for the proper voltageneeded. Switch the power On and verify the following on the Control
Panel (Figure 2-l):a.
The alternating two tone audible alarm sounds and all displaysand indicators are lit for approximately two seconds.
Note:
During this time the controller also performs self check
functions. If the controller detects a failure, the alarm stays on
and service is required.
Note:
All alarms except system failure or power failure are pre-
ceded by a 30 second intermittent operator prompt tone.
b.
The manual mode indicator is lit.
c.
Operator prompt tones sound and the % power display flashes.
2.
Adjust the heat output with the increase (A) and decrease
switches to attain the high and low limits as indicated by the %
power display.
(v)
touch
Note: Steps 3 through 8 do not apply to the model 2001 International.
3.
Connect the skin temperature probe to the warmer.
4.
Press the mode touch switch to place the warmer in the servo modeand verify the following:
Note:
An alternating two tone alarm, a flashing overhead alarm lightand the patient temperature display flashing if the skin temperature probe is below 30°C. Warm the probe with
your fingers or silence the alarm.
a.
The servo mode indicator is lit.
b.
An operator prompt tone sounds and the control temperature
display flashes
5.
Press the increase (A) touch switch and verify that the maximum
servo control temperature attainable is
Note:
the patient temperature and the control temperature is greater thanperson).
6.
Press the decrease touch switch and verify that the minimum servocontrol temperature attainable is
A patient temperature alarm occurs if the difference between1°C (the difference can be adjusted to
36.5”C.
0.5”C
35.O”C.
“LL.L”
may occur here
37.5”C.
by a qualified service
7.
Disconnect the skin temperature probe. Verify the following:
a.
The probe failure indicator light is lit.
b.
There is an alternating two tone alarm.
C.
The overhead alarm light is flashing.
d.
The patient temperature display flashes
6600-0194-000
11/09/93
“HH.H”.
2-5
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