Stryker CUB FL19H User manual

CCUUBB®® PPeeddiiaattrriicc CCrriibb
OOppeerraattiioonnss MMaannuuaall
FL19H (1900)
EN
1900-109-001 REV C.0 2019/08

SSyymmbboollss
General Warning
Caution
Operating instructions/Consult instructions for use
Type BF applied part
IIPPXX44 Protection from liquid splash
Direct Current
Medical Equipment approved by the Canadian Standards Association with Respect to Electric Shock, Fire,
Mechanical and Other Specified Hazards
In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic Equipment (WEEE)
as amended, this symbol indicates that the product should be collected separately for recycling. Do not
dispose of as unsorted municipal waste. Contact local distributor for disposal information. Ensure infected
equipment is decontaminated prior to recycling.
Catalogue number

Serial number
Manufacturer
Date of manufacture
1900-109-001 REV C.0 EN

TTaabbllee ooff CCoonntteennttss
Warning/Caution/Note Definition ..............................................................................................................................3
Summary of safety precautions ................................................................................................................................4
Introduction ...............................................................................................................................................................6
Product description .................................................................................................................................................6
Indications for use...................................................................................................................................................6
Expected service life ...............................................................................................................................................6
Contraindications....................................................................................................................................................6
Specifications .........................................................................................................................................................6
Product illustration ..................................................................................................................................................8
Contact information.................................................................................................................................................9
Serial number location.............................................................................................................................................9
Setup.......................................................................................................................................................................10
Operation ................................................................................................................................................................11
Base controls........................................................................................................................................................11
Applying and releasing the brakes..........................................................................................................................12
Transporting a patient with the retractable fifth wheel...............................................................................................12
Raising the litter....................................................................................................................................................12
Lowering the litter..................................................................................................................................................12
Positioning the product in Trendelenburg ................................................................................................................13
Positioning the product in Reverse Trendelenburg...................................................................................................13
Raising or lowering the manual Fowler backrest ......................................................................................................14
Raising or lowering the pneumatic Fowler backrest..................................................................................................14
Raising or lowering the foot section ........................................................................................................................14
Raising the siderail................................................................................................................................................14
Lowering the siderail .............................................................................................................................................15
Opening the access doors (option) .........................................................................................................................16
Closing the access doors (option)...........................................................................................................................16
Scale control panel (option) ...................................................................................................................................16
Weighing a patient............................................................................................................................................17
Setting the scale memory..................................................................................................................................18
Zeroing the scale..............................................................................................................................................18
Changing equipment ........................................................................................................................................18
Changing the scale units...................................................................................................................................18
Replacing the scale batteries (scale option)........................................................................................................18
Accessories ............................................................................................................................................................20
Standard accessory bracket...................................................................................................................................20
Premium accessory bracket (option).......................................................................................................................21
Securing the oxygen bottle into the retaining collar (option) ......................................................................................21
Attaching the upright oxygen bottle holder...............................................................................................................22
Attaching the defibrillator tray.................................................................................................................................23
Attaching the IV caddy...........................................................................................................................................23
Positioning the two-stage permanently attached IV pole (option)...............................................................................24
Positioning the three-stage permanently attached IV pole (option) ............................................................................25
Attaching and positioning the removable IV pole (FA64135) .....................................................................................26
Attaching and positioning the removable IV pole (FDTSH) .......................................................................................27
Chart holder / monitor holder (option) .....................................................................................................................27
Installing the retracting protective top......................................................................................................................28
Positioning the retracting protective top ..................................................................................................................29
Installing the protective top with supports................................................................................................................29
Positioning the protective top with supports.............................................................................................................30
Preventive maintenance .........................................................................................................................................32
Cleaning and disinfecting with wipes......................................................................................................................34
Cleaning..................................................................................................................................................................35
1900-109-001 REV C.0 1 EN

Disinfecting .............................................................................................................................................................36
EN 2 1900-109-001 REV C.0

WWaarrnniinngg//CCaauuttiioonn//NNoottee DDeeffiinniittiioonn
The words WWAARRNNIINNGG,CCAAUUTTIIOONN, and NNOOTTEE carry special meanings and should be carefully reviewed.
WWAARRNNIINNGG
Alerts the reader about a situation which, if not avoided, could result in death or serious injury. It may also describe
potential serious adverse reactions and safety hazards.
CCAAUUTTIIOONN
Alerts the reader of a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the
user or patient or damage to the product or other property. This includes special care necessary for the safe and effective
use of the device and the care necessary to avoid damage to a device that may occur as a result of use or misuse.
NNoottee -- Provides special information to make maintenance easier or important instructions clearer.
1900-109-001 REV C.0 3 EN

SSuummmmaarryy ooff ssaaffeettyy pprreeccaauuttiioonnss
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WWAARRNNIINNGG
• Always allow the product to reach room temperature before you set up the product or test functional operations.
Permanent product damage may occur.
• Always operate the product when all operators are clear of the mechanisms.
• Always apply the brakes when a patient is getting on the product or off the product or when the product is not moving.
Injury could result if the product moves while a patient is getting on the product or off the product.
• Always position the patient in the center of the product.
• Always remove any devices that may be in the way before you raise or lower the litter.
• Always lock the siderails in the full up position with the sleep surface flat in the lowest position when you transport a
patient.
• Do not move the crib sideways with the fifth wheel applied.
• Always put the product in the lowest position with the siderails up and latched and access doors closed and locked when
you leave a patient unattended on the product. Do not leave the product at a higher height.
• Always put the siderails up and latched when you put the product in a Trendelenburg position.
• Make sure that the support arm is secure in the arm supports before you release the Fowler or foot section.
• Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you
transport a patient.
• Always keep operator and patient limbs away from the siderails when you raise or lower the siderail.
• Always make sure that the open/close indicators show green when the door is closed.
• Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray. Always strap down all devices that you
place on the defibrillator tray.
• Always secure the IV pole to the IV caddy when you transport the product.
• Always store the IV caddy when not in use to avoid product damage.
• Make sure that the IV pole is positioned correctly so that the patient cannot reach or manipulate the IV pole.
• Do not use the IV pole as a push/pull device. Product damage may occur.
• For removable IV pole FDTSH, do not hang IV bags that exceed 11 lb (5 kg).
• Patient must be moved from product before installing a protective top.
• On a product with scale, make sure that the scale is turned off before installing a protective top.
• Make sure that the protective top is secure and functions before returning the product to service.
• Always make sure that both lower rails are in the locked position before leaving a patient unattended.
• Always make sure that you use the center of the lower rail to close the protective top.
CCAAUUTTIIOONN
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this
manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation
resulting in injury to patient or operator. Modifying the product also voids its warranty.
• Do not lean on the bracket of the scale module.
• Do not use a foot end fixed IV pole on a product with the scale option.
• Always make sure external equipment is removed from product litter when zeroing the scale or weighing the patient.
• Zero the scale at least once a week to maintain scale accuracy.
• Always use 1.5 VDC alkaline batteries.
• Remove the batteries from the product during long periods of disuse.
• Do not load the IV pole above the safe working load of 40 lb (18 kg).
• Do not load an IV pole hook above the safe working load of 11 lb (5 kg).
• Do not use the protective top as a push/pull device. Product damage may occur.
• Do not clean, disinfect, service, or perform maintenance while the product is in use.
EN 4 1900-109-001 REV C.0

• Always clean VVeellccrroo®® after each use. Saturate VVeellccrroo with disinfectant and allow disinfectant to evaporate. Appropriate
disinfectant for nylon VVeellccrroo should be determined by the hospital.
• Always wipe down with clean water and dry each product after disinfecting. Some disinfectants are corrosive in nature
and may cause damage to the product. If you do not rinse and dry the product, you may leave a corrosive residue on the
surface of the product. This corrosive residue could cause premature degradation of critical components. Failure to
follow these disinfecting instructions may void your warranty.
• Do not use quaternary disinfectants formulated with glycol ethers.
•VViirreexx®® TB is not an approved cleaning agent for this product. Do not use for crib cleaning.
1900-109-001 REV C.0 5 EN

IInnttrroodduuccttiioonn
This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating or
maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or maintenance
of this product.
CCAAUUTTIIOONN
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this
manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation
resulting in injury to patient or operator. Modifying the product also voids its warranty.
NNoottee
• This manual is a permanent part of the product and should remain with the product even if the product is sold.
• Stryker continually seeks advancements in product design and quality. This manual contains the most current product
information available at the time of printing. There may be minor discrepancies between your product and this manual. If
you have any questions, contact Stryker Customer Service or Technical Support at 1-800-327-0770.
PPrroodduucctt ddeessccrriippttiioonn
The Stryker Model FL19H CCUUBB®® pediatric crib is a pediatric medical crib that consists of moveable and latchable rails, an
accompanying mattress, and an adjustable bed surface.
IInnddiiccaattiioonnss ffoorr uussee
The Stryker Model FL19H CCUUBB pediatric crib is intended to provide a pediatric patient support surface for medical purposes
and to provide a method of transporting pediatric patients within a healthcare facility.
EExxppeecctteedd sseerrvviiccee lliiffee
CCUUBB pediatric cribs have a 10 year expected service life under normal use conditions and with appropriate periodic
maintenance.
CCoonnttrraaiinnddiiccaattiioonnss
None known.
SSppeecciiffiiccaattiioonnss
Safe working load
NNoottee:: Safe working load indicates the sum of the occupant and
accessory weight. 100 lb 45 kg
Product weight capacity 400 lb 181 kg
Product weight 375 lb 170 kg
Scale system capacity (optional equipment), loads weighing up to: 4 lb to 100 lb 1.8 kg to 54.4 kg
EN 6 1900-109-001 REV C.0

Scale system accuracy (optional equipment) Perform scale measurement when
unit is flat:
± 0.5 lb (0.2 kg) for patients
weighing 50 lb (22 kg) or less
± 1.0 lb (0.4 kg) for patients
weighing ≥ 50 lb (22 kg)
Height range (to litter top) High 40 in 102 cm
Low 33 in 84 cm
Patient sleep surface 29.5 in x 57 in 75 cm x 145 cm
Litter position
Manual activated 0° / 25° / 40° / 55°
Pneumatic assist 0° - 50°
Trendelenburg/Reverse Trendelenburg ± 9.5°
Foot section angle 0° / 6° / 12°
Power system (for scale option) Battery operated: 4 x C type,
alkaline, 1.5 VDC
Electrical requirements (for scale option) 6 VDC, 0.15 A
CCoommppaattiibbllee mmaattttrreessss
55-0072 58.25 in. x 30.13 in. x 4 in. 148 cm x 76.53 cm x 10.16
cm
EEnnvviirroonnmmeennttaall ccoonnddiittiioonnss OOppeerraattiioonn SSttoorraaggee aanndd ttrraannssppoorrttaattiioonn
Ambient temperature
85 °F
(29.1 °C)
60 °F
(15.5 °C)
122 °F
(50 °C)
-22 °F
(-30 °C)
Relative humidity (non-condensing)
95%
0%
95%
0%
Atmospheric pressure
1060 hPa
700 hPa
1060 hPa
500 hPa
Specifications listed are approximate and may vary slightly from product to product or by power supply fluctuations.
Stryker reserves the right to change specifications without notice.
SSttaannddaarrddss aapppplliieedd
CAN/CSA C22.2 No. 601.1-M90 (AM1 + AM2) Medical Electrical Equipment - Part 1: General
Requirements for Safety - General Instruction No 1; Update
No 2
UL60601-1 Medical Electrical Equipment, Part 1: General
Requirements for Safety
IEC 60601-1: 1988 (AM1 + AM2) Medical Electrical Equipment Part 1: General
Requirements for Safety - Edition 2.0; Amendment 1: 11-
1991, Amendment 2: 03-1995, Corrigendum 1: 6-1995,
CENELEC EN 60601-1:1990
1900-109-001 REV C.0 7 EN

PPrroodduucctt iilllluussttrraattiioonn
ABC
D
GH
I
J
K
L
MNOP
Q
R
E
F
FFiigguurree 11 –– PPrroodduucctt iilllluussttrraattiioonn
AFowler J Scale module (option)
BSiderail KSiderail activiation handle
C Endrail LLitter lift pedal
DAccess door (option) MGround chain
EAccess door release knobs (option) NUni-lower pedal
FBrake/steer pedal (option) O Pneumatic head section activation lever
G Foot section P IV caddy arm (option)
HDrainage bag hook QOxygen bottle retaining collar (option)
IFoot section support arm RPremium accessory brackets (option)
EN 8 1900-109-001 REV C.0

CCoonnttaacctt iinnffoorrmmaattiioonn
Contact Stryker Customer Service or Technical Support at: 1-800-327-0770.
Stryker Medical
3800 E. Centre Avenue
Portage, MI 49002
USA
To view your operations or maintenance manual online, see https://techweb.stryker.com/.
Have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical Support.
Include the serial number in all written communication.
SSeerriiaall nnuummbbeerr llooccaattiioonn
You can find the serial number (A) on the right foot end of the litter frame (Figure 2).
A
FFiigguurree 22 –– SSeerriiaall nnuummbbeerr llooccaattiioonn
1900-109-001 REV C.0 9 EN

SSeettuupp
To unpack your product, see the unpacking instructions that are attached to the product inside of the shipping crate.
WWAARRNNIINNGG
• Always allow the product to reach room temperature before you set up the product or test functional operations.
Permanent product damage may occur.
• Always operate the product when all operators are clear of the mechanisms.
Make sure that the product is working before you put the product into service.
1. Apply the brake. Push on the product to make sure that all four casters are locked.
2. Release the brake. Push on the product to make sure that all four casters are unlocked.
3. Raise and lower the litter with the hydraulic lift system.
4. Raise the product to the highest position and put the product in the Trendelenburg position. Make sure that the head end
lowers to the full down position.
5. Raise the product to the highest position and put the product in the Reverse Trendelenburg position. Make sure that the
foot end lowers to the full down position.
6. Apply the fifth wheel (option) and make sure that it guides and pivots the product.
7. Make sure that the access doors (option) open, close, and lock.
8. Make sure that the side/endrails raise, lower, and lock in the 9 in. (option), 14 in., and upper position.
9. Raise and lower the manual Fowler backrest (head section).
10.Raise and lower the manual foot section.
EN 10 1900-109-001 REV C.0

OOppeerraattiioonn
BBaassee ccoonnttrroollss
HEAD END
RIGHT
LEFT
AB
B
A
C
C
D
D
E
E
FFiigguurree 33 –– BBaassee ccoonnttrroollss
APump to raise the litter
BLowers both ends of the product together
CPlaces the product in the Trendelenburg position
(head down, foot up)
DPlaces the product in the Reverse Trendelenburg
position (head up, foot down)
EBrake and steer functions
1900-109-001 REV C.0 11 EN

AAppppllyyiinngg aanndd rreelleeaassiinngg tthhee bbrraakkeess
WWAARRNNIINNGG -- Always apply the brakes when a patient is getting on the product or off the product or when the product is not
moving. Injury could result if the product moves while a patient is getting on the product or off the product.
To apply the brakes, push down on the brake (red) side of the brake/steer pedal (E) (
Base controls (page 11)). Push on the
product to make sure that the brakes work.
To release the brakes, push down on the steer (green) side of the brake/steer pedal (E) (
Base controls (page 11)).
TTrraannssppoorrttiinngg aa ppaattiieenntt wwiitthh tthhee rreettrraaccttaabbllee ffiifftthh wwhheeeell
WWAARRNNIINNGG
• Always position the patient in the center of the product.
• Always remove any devices that may be in the way before you raise or lower the litter.
• Always lock the siderails in the full up position with the sleep surface flat in the lowest position when you transport a
patient.
• Do not move the crib sideways with the fifth wheel applied.
To transport a patient with the retractable fifth wheel:
1. Push down on the steer side of the brake/steer pedal (E) to apply the fifth wheel (
Base controls (page 11)).
2. Put the pedal in the neutral position to move the product laterally. Move the product to the desired location.
3. Apply the brakes to lock the product in place.
NNoottee -- Always make sure that the brake is released before you move the product to avoid operator or patient injury.
RRaaiissiinngg tthhee lliitttteerr
WWAARRNNIINNGG
• Always position the patient in the center of the product.
• Always put the product in the lowest position with the siderails up and latched and access doors closed and locked when
you leave a patient unattended on the product. Do not leave the product at a higher height.
• Always remove any devices that may be in the way before you raise or lower the litter.
To raise the litter, press down on the pump pedal (A) until you achieve the desired height (
Base controls (page 11)).
LLoowweerriinngg tthhee lliitttteerr
WWAARRNNIINNGG
• Always position the patient in the center of the product.
• Always put the product in the lowest position with the siderails up and latched and access doors closed and locked when
you leave a patient unattended on the product. Do not leave the product at a higher height.
• Always remove any devices that may be in the way before you raise or lower the litter.
To lower the entire litter, press down on the center of the uni-lower pedal (B) (
Base controls (page 11)).
To lower the head end of the litter, press down on the side of the uni-lower pedal (C) closest to the head end of the product
(
Base controls (page 11)).
To lower the foot end of the litter, press down on the side of the uni-lower pedal (D) closest to the foot end of the product
(
Base controls (page 11)).
EN 12 1900-109-001 REV C.0

PPoossiittiioonniinngg tthhee pprroodduucctt iinn TTrreennddeelleennbbuurrgg
WWAARRNNIINNGG
• Always put the siderails up and latched when you put the product in a Trendelenburg position.
• Always remove any devices that may be in the way before you raise or lower the litter.
To position the product in the Trendelenburg position (head down), Raise the litter to the highest height (
Raising the litter
(page 12)).
NNoottee -- Raise the litter to the highest height for a greater Trendelenburg angle.
To lower the head end of the product, push down on the side of the uni-lower pedal (C) closest to the head end (
Base
controls
(page 11)).
To lower the product from Trendelenburg position, push down on the center of the uni-lower pedal (B) until the litter is flat
(
Base controls (page 11)).
PPoossiittiioonniinngg tthhee pprroodduucctt iinn RReevveerrssee TTrreennddeelleennbbuurrgg
WWAARRNNIINNGG
• Always put the siderails up and latched when you put the product in a Trendelenburg position.
• Always remove any devices that may be in the way before you raise or lower the litter.
To position the product in the Reverse Trendelenburg position (foot down), raise the litter to the highest height (
Raising the
litter
(page 12)).
NNoottee -- Raise the litter to the highest height for a greater Trendelenburg angle.
To lower the foot end of the product, push down on the side of the uni-lower pedal (D) closest to the foot end (
Base controls
(page 11)).
To lower the product from Reverse Trendelenburg position, push down on the center of the uni-lower pedal (B) until the
litter is flat (
Base controls (page 11)).
1900-109-001 REV C.0 13 EN

RRaaiissiinngg oorr lloowweerriinngg tthhee mmaannuuaall FFoowwlleerr bbaacckkrreesstt
WWAARRNNIINNGG
• Always position the patient in the center of the product.
• Make sure that the support arm is secure in the arm supports before you release the Fowler or foot section.
To raise the Fowler backrest, lift up the Fowler backrest (A) until the support arm is secure in the desired position (25°, 40°,
and 55°) (
Product illustration (page 8)).
To lower the Fowler backrest, lift up the Fowler backrest (A) to release the support arm and lower the Fowler backrest down
to the desired position (0°, 25°, 40°, and 55°) (
Product illustration (page 8)).
RRaaiissiinngg oorr lloowweerriinngg tthhee ppnneeuummaattiicc FFoowwlleerr bbaacckkrreesstt
WWAARRNNIINNGG -- Always position the patient in the center of the product.
To raise the Fowler backrest, lift up the head section activation lever (O), raise the Fowler backrest (A) to the desired
position (0° - 50°), and release the activation lever (
Product illustration (page 8)).
To lower the Fowler backrest, lift up the head section activation lever (O), push down on the Fowler backrest (A) to the
desired position (0° - 50°), and release the activation lever (
Product illustration (page 8)).
RRaaiissiinngg oorr lloowweerriinngg tthhee ffoooott sseeccttiioonn
WWAARRNNIINNGG
• Always position the patient in the center of the product.
• Make sure that the support arm is secure in the arm supports before you release the Fowler or foot section.
To raise the foot section, lift up the foot section (G) until the support arm (I) is secure in the desired position (6° and 12°)
(
Product illustration (page 8)).
To lower the foot section, lift up the foot section (G) to release the support arm (I) and lower the foot section down to the
desired position (0°, 6°, and 12°) (
Product illustration (page 8)).
RRaaiissiinngg tthhee ssiiddeerraaiill
WWAARRNNIINNGG
• Always put the product in the lowest position with the siderails up and latched and access doors closed and locked when
you leave a patient unattended on the product. Do not leave the product at a higher height.
• Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you
transport a patient.
• Always keep operator and patient limbs away from the siderails when you raise or lower the siderail.
To raise the siderail/endrail:
1. Use two hands to grasp the siderail.
2. Lift the siderail until the siderail is secure in the desired position (9 in., 14 in., and 26 in.).
3. Pull on the siderail to make sure that the siderail is latched and the arrow pointers (A) are aligned (Figure 4).
EN 14 1900-109-001 REV C.0

A
FFiigguurree 44 –– SSiiddeerraaiill aarrrrooww ppooiinntteerrss
LLoowweerriinngg tthhee ssiiddeerraaiill
WWAARRNNIINNGG
• Always put the product in the lowest position with the siderails up and latched and access doors closed and locked when
you leave a patient unattended on the product. Do not leave the product at a higher height.
• Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you
transport a patient.
• Always keep operator and patient limbs away from the siderails when you raise or lower the siderail.
To lower the siderail/endrail:
1. Grasp the siderail activation handle (B), press the activation trigger, and turn the handle left or right (Figure 5).
B
FFiigguurree 55 –– SSiiddeerraaiill aaccttiivvaattiioonn hhaannddllee
2. Lower the siderail until the siderail is at the desired position (9 in., 14 in., and 26 in.) and release the siderail activation
handle.
NNoottee
• Siderails automatically stop at the 9 in. position while lowering the siderail.
• The double safety lock at the 9 in. position may not be present on all products.
3. Pull on the siderail to make sure that the siderail is latched and the arrow pointers (A) are aligned (Figure 4).
1900-109-001 REV C.0 15 EN

OOppeenniinngg tthhee aacccceessss ddoooorrss ((ooppttiioonn))
To open the access doors:
1. Squeeze the release knobs (A) to release the access door (Figure 6).
NNoottee -- The open/close indicators (B) will show yellow when the door is released from the lock (Figure 7).
A
FFiigguurree 66 –– AAcccceessss ddoooorr
B
FFiigguurree 77 –– OOppeenn//cclloossee iinnddiiccaattoorrss
CClloossiinngg tthhee aacccceessss ddoooorrss ((ooppttiioonn))
WWAARRNNIINNGG -- Always make sure that the open/close indicators show green when the door is closed.
To close the access doors:
1. Return the door to the closed position.
NNoottee -- The open/close indicators (B) will show green when the door is locked in the closed position (Figure 7).
SSccaallee ccoonnttrrooll ppaanneell ((ooppttiioonn))
CCAAUUTTIIOONN
• Do not lean on the bracket of the scale module.
• Do not use a foot end fixed IV pole on a product with the scale option.
EN 16 1900-109-001 REV C.0