Operating instructions/Consult instructions for use
General warning
Caution
Warning; electricity
Fuse rating
Do not drill
Hydraulic oil pressure
Pinch/crush hazard
Non-ionizing radiation
Catalogue number
Serial number
European medical device
CE mark
5900-009-002 Rev A.0EN
Authorized representative in the European Community
For US Patents see www.stryker.com/patents
Manufacturer
Safe working load
~
≤2m ≥18m
87VL
Mass of equipment
Maximum patient weight
Adult patient biometrics
Alternating current
Direct current
Duty cycle of product
Unit provides terminal for connection of a potential equalization conductor. The potential
equalization conductor provides direct connection between the unit and potential equalization
busbar of the electrical installation.
Protective earth ground
IIPPXX44
Protection from liquid splash
Type B applied part
Medical Equipment Classified by Underwriters Laboratories Inc. With Respect to Electric Shock,
Fire, and Mechanical Hazards Only in Accordance with ANSI/AAMI ES60601-1:2005/(R)2012
and A1:2012 C1:2009/(R)2012 and A2:2010/(R)2012, CAN/CSA-C22.2 No. 60601-1:14, IEC
60601-2-52:2009/A1:2015, CAN/CSA-C22.2 No. 60601-2-52:11 with Amendment 1:2017.
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.
Summary of safety precautions ................................................................................................................................4
Indications for use ...................................................................................................................................................5
Expected service life ...............................................................................................................................................5
Contact information .................................................................................................................................................8
Serial number location.............................................................................................................................................9
Maintenance menu ................................................................................................................................................. 20
Set clock .............................................................................................................................................................. 20
Test modes ..........................................................................................................................................................24
Service ....................................................................................................................................................................25
Protecting against electrostatic discharge (ESD) .....................................................................................................25
Main control board replacement .............................................................................................................................26
Footboard main cable replacement ........................................................................................................................28
Siderail replacement, head end..............................................................................................................................33
IV pole attachment ................................................................................................................................................34
Top level assembly .................................................................................................................................................36
Deck pan assembly, seat deck, patient right.......................................................................................................... 54
5900-009-002 Rev A.01EN
Deck pan assembly, seat deck, patient left ............................................................................................................ 55
Deck assembly, head section ................................................................................................................................. 56
Deck pan assembly, head deck, patient right......................................................................................................... 65
Deck pan assembly, head deck, patient left ...........................................................................................................66
Lock assembly, head deck position........................................................................................................................ 67
Deck pan assembly, knee deck, patient right.........................................................................................................72
Deck pan assembly, knee deck, patient left ...........................................................................................................73
Deck pan assembly, foot deck, patient right...........................................................................................................81
Deck pan assembly, foot deck, patient left .............................................................................................................82
HILO frame assembly ............................................................................................................................................. 83
Rail assembly, head ...............................................................................................................................................93
Timing link assembly ............................................................................................................................................ 108
Rail arm assembly, power/communication........................................................................................................... 109
Rail arm assembly, nurse call/speaker................................................................................................................. 110
Rail arm assembly, no cable................................................................................................................................. 111
Latch lock assembly, left head/right foot - 5900200023....................................................................................... 113
Latch lock assembly, right head/left foot - 5900200024....................................................................................... 114
Power supply cord ................................................................................................................................................ 115
Accessory cord, type B 120V................................................................................................................................ 116
EMC information ................................................................................................................................................... 123
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.
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WWAARRNNIINNGG
• Always use this product for bariatric use only per the details on the product labeling and specifications from this manual.
• Do not use this product for psychiatric, pediatric, or home health care use.
• Do not use this product in an oxygen rich environment.
• Always use Stryker approved mattresses that have been tested for compatibility with the product frame to avoid the risk
of patient entrapment.
• Do not lower the litter too low or the litter may not be supported.
• The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could
result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper operation.
• Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should
be no closer than 12 inches (30 cm) to any part of MMVV33, including cables specified by the manufacturer.
• Avoid stacking or placing equipment adjacent with other equipment to prevent improper operation of the products. If
such use is necessary, carefully observe stacked or adjacent equipment to make sure that they are operating properly.
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.
• Always make sure that the product is clear of obstacles before you use motion functions.
• Always calibrate the product angles when you replace the main control board or any actuator or product damage may
occur.
• Always use ESD protective equipment before opening antistatic bags and servicing electronic parts.
• Do not place unprotected circuit boards on the floor.
• Always perform this procedure in a secure location with the floor jack secure to the base frame before you remove the
caster to prevent the risk of injury.
• Do not put your hands or feet below the caster when you remove or attach the caster to prevent the risk of injury.
• Always leave the bolts loose in the support holes, so the bolt head is out far enough to stop the lift mechanism slide
block.
EN45900-009-002 Rev A.0
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 5900 MMVV33™™ bariatric hospital bed is an AC-powered adjustable hospital bed designed to be utilized with
a patient support surface matching the deck size of the bed frame. MMVV33 consists of a Fowler and knee Gatch to aid in the
adjustment of the surface contour of the bed, moveable and latchable siderails, and electronic controls located in the
footboard and siderails. The
positioning and provides visual alerts when those parameters set by the health care professional (HCP) are altered.
ii
BBeedd®® Awareness system allows users to set various bed parameters to monitor bed
IInnddiiccaattiioonnss ffoorr uussee
WWAARRNNIINNGG
• Always use this product for bariatric use only per the details on the product labeling and specifications from this manual.
• Do not use this product for psychiatric, pediatric, or home health care use.
• Do not use this product in an oxygen rich environment.
The MMVV33 bariatric bed is intended to provide a patient support surface for medical purposes and to provide a method of
transporting patients within a healthcare facility. It is intended to be used with bariatric, adult, non-behavioral health patients
with a BMI of 30 kg/m² or greater and weighing 250 lb (113.4 kg) or more.
CClliinniiccaall bbeenneeffiittss
Patient treatment, patient positioning, and diagnostic
EExxppeecctteedd sseerrvviiccee lliiffee
The 5900 MMVV33 bariatric bed has an eight year expected service life under normal use conditions and with appropriate
periodic maintenance.
The backup batteries have a one year expected service life under normal use conditions.
DDiissppoossaall//rreeccyyccllee
Always follow the current local recommendations and/or regulations governing environmental protection and the risks
associated with recycling or disposing of the equipment at the end of its useful life.
5900-009-002 Rev A.05EN
CCoonnttrraaiinnddiiccaattiioonnss
None known.
SSppeecciiffiiccaattiioonnss
WWAARRNNIINNGG -- Always use Stryker approved mattresses that have been tested for compatibility with the product frame to
avoid the risk of patient entrapment.
Safe working load
NNoottee:: Safe working load indicates the sum of the
occupant, accessories, and mattress weight.
1102 lb
500 kg
Maximum patient weight
Product weight
Scale system capacity maximum1102 lb500 kg
± 4.4 lb (2 kg) for patients weighing 225 (102 kg)
to 882 lb (400 kg)
Scale system accuracy
± 6.6 lb (3 kg) for patients weighing 886 (402 kg)
to 1102 lb (500 kg)
92 in. x 38.3 in.233.7 cm x 97.2 cm
Overall length and width
Patient sleep surface
Siderails stowed
Siderails at low,
intermediate, and high
position
36 in. (91.4 cm) deck
position
42 in. (106.7 cm) deck
position
92 in. x 42 in.233.7 cm x 106.7 cm
92 in. x 48 in.233.7 cm x 121.9 cm
92 in. x 40.5 in.233.7 cm x 102.9 cm
92 in. x 46.5 in.233.7 cm x 118.1 cm
92 in. x 52.5 in.233.7 cm x 133.4 cm
80 in. x 34.5 in.
80 in. x 40.5 in.
1027 lb
902 lb
203.2 cm x 87.6 cm
203.2 cm x 102.9 cm
465.8 kg
409.1 kg
48 in. (121.9 cm) deck
position
Bed height to top of seat litter
Knee Gatch position0° to 20° ± 2°
Fowler position
Foot position
Trendelenburg and reverse Trendelenburg
Electrical requirements
NNoottee -- Class I Electrical Equipment: Protection against electrical
shock relies on connection to protective earth of an appropriately
rated hospital grade outlet.
Hospital grade GFCI auxiliary outlet
EN65900-009-002 Rev A.0
80 in. x 46.5 in.
12 in. to 28 in.30.5 cm to 71.1 cm
0° to 60° ± 2°
0° to 13° ± 2°
+12° to -12°
120 VAC, 60 Hz, 8A230 VAC, 50 Hz, 4A
120 VAC, 60 Hz, 6A
203.2 cm x 118.1 cm
230 VAC, 50 Hz, 3A
Battery voltage
95 °F
(35 °C)
50 °F
(10 °C)
140 °F
(60 °C)
-40 °F
(-40 °C)
80%
20%
95%
10%
106 kPa
70 kPa
106 kPa
50 kPa
NNoottee -- Always replace with Stryker approved batteries.
12 VDC (x2) (Stryker part number: 5900280025)
Duty cycle
2 minutes ON, 18 minutes OFF
Application environments1, 2, 3, and 5 per IEC 60601-2-52
Maximum acoustic sound pressure
< 60 dBA
CCoommppaattiibbllee mmaattttrreessss
Bariatric non-powered
support surface
Length
WidthThickness
Bolster width,
patient right and
patient left
Bolster
thickness,
patient right and
patient left
(28850555001)
79.5
in.
201.9cm45 in.114.3cm7 in.17.8
cm
6 in.15.2
cm
7 in.17.8
NNoottee -- Minimum mattress firmness: ILD at 50% - minimum of 108 lbf
Stryker reserves the right to change specifications without notice.
Specifications listed are approximate and may vary slightly from product to product or by power supply fluctuations.
Contact Stryker Customer Service or Technical Support at: 1-800-327-0770.
Stryker Medical
3800 E. Centre Avenue
Portage, MI 49002
USA
EN85900-009-002 Rev A.0
NNoottee -- The user and/or the patient should report any serious product-related incident to both the manufacturer and the
A
Competent authority of the European Member State where the user and/or patient is established.
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) below the headboard at the head of the bed (Figure 2).
Remove the product from service before you perform the preventive maintenance inspection. Make sure that all items listed
during annual preventive maintenance for all Stryker Medical products. You may need to perform preventive maintenance
checks more often based on your level of product usage. Service only by qualified personnel.
NNoottee -- Clean and disinfect the exterior of the support surface before inspection, if applicable.
Inspect the following items:
All welds
All fasteners are secure
Casters lock with brake pedal applied
Casters are secure and swivel
Casters are free of wax and debris
Center light LED and bumper LEDs flash when brakes are released
Steer function works
Siderails move, latch, and stow
Deck expands, retracts, and locks in all positions
CPR release operates
IV pole is intact and operates (option)
Foley bag hooks intact
No cracks or splits in headboard, footboard or siderail panels
No rips or cracks in mattress cover
All functions on head end siderails operate (includes LEDs)
All functions on footboard operate (includes LEDs)
No cracks or damage to control overlays
Scale system calibrated
Night light operates
Power cords and plug not frayed or damaged
No cables worn or pinched
No damage to nurse call connections
All electrical connections tight
All ground strap cables are secure to the frame
Ground impedance not more than 200 mΩ (milliohms)
Current leakage not more than 300 µA (microamps)
Apply grease to the litter grease points (see maintenance manual for locations)
Ground chains intact
Trendelenburg/reverse Trendelenburg angle accuracy is minimum +12° to -12°
Fowler angle accuracy is 0° - 60° ± 2°
Fowler holds position at 30° with weight
Siderail switches operate (iiBBeedd Awareness)
Center light LED and bumper LEDs operate (iiBBeedd Awareness)
Inspect footboard control labels for signs of degradation
EN105900-009-002 Rev A.0
Inspect hi-lo actuators for oil leaks
Inspect footboard connector housing for cracks or damage
All motions function
Nurse call functions
Auxiliary outlets function (test ground fault interrupter)
Replace batteries (one year expected service life)
Set clock to local date and time
Product serial number:
Completed by:
Date:
5900-009-002 Rev A.011EN
EErrrroorr ccooddeess
Error codes are detailed in the table below.
EErrrroorr ccooddeeCCaauussee
0.02Error on non volatile memory
(nvm)
0.03Watchdog switch in wrong position or broken
(comWatchdogDisabled)
0.04Software version mismatched or missing board
(softwareVersionMismatch)
0.05Brake switch malfunction
(brake)
0.06Obstruction switch malfunction
(obstruction)
0.07CPR switch/cable malfunction
(cprHandle)
0.08FSC_KPD board is not responding
(FSC_KPD_missing)
TTrroouubblleesshhoooottiinngg
1. Reboot product
2. Replace MCU
1. Toggle watchdog switch on MCU
1. Reboot product
2. Check for a missing board error, if missing take
corrective action on cable or board
1. Check brake cable and switch
1. Check each of the four obstruction switches and
cables
1. Check CPR switch, cable, and head actuator
1. Check cable
2. Check AVB board (electrical issue)
0.09FSC_GUI board is not responding
(FSC_GUI_missing)
0.1SRK PL board is not responding
(SRK_PL_missing)
0.11SRK PR board is not responding
(SRK_PR_missing)
0.12PSI board is not responding
(PSI_missing)
1. Check cable
2. Check FSC_KPD
•Software in bootloader mode
•Software incorrect
•Electrical issue
3. AVB board (electrical issue)
1. Check cables
2. Check junction boards
3. Check SRK board
4. Check SRC (software and electrical)
1. Check cables
2. Check junction boards
3. Check SRK board
4. Check SRC (software and electrical)
1. Check cables
2. Check junction boards
EN125900-009-002 Rev A.0
EErrrroorr ccooddeeCCaauussee
TTrroouubblleesshhoooottiinngg
0.13ACB HILO foot board is not responding
(ACB_HILO_FT_missing)
0.14ACB HILO head board is not responding
(ACB_HILO_HD_missing)
0.15ACB foot board is not responding
(ACB_FT_missing)
0.16ACB head board is not responding
(ACB_HD_missing)
0.17ACB knee board is not responding
(ACB_KN_missing)
0.18SRC foot patient left board is not responding
(SRC_FT_PL_missing)
0.19SRC head patient left board is not responding
(SRC_HD_PL_missing)
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
0.2SRC foot patient right board is not responding
(SRC_FT_PR_missing)
0.21SRC head patient right board is not responding
(SRC_HD_PR_missing)
0.22DPM foot board is not responding
(DPM_FT_missing)
0.23DPM head board is not responding
(DPM_HD_missing)
0.24DPM MID board is not responding
(DPM_MID_missing)
0.25SMB foot board is not responding
(SMB_FOOT_missing)
0.26SMB head board is not responding
(SMB_HEAD_missing)
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
1. Check cables
2. Check junction boards
5900-009-002 Rev A.013EN
EErrrroorr ccooddeeCCaauussee
TTrroouubblleesshhoooottiinngg
0.27AVB board is not responding
(AVB_missing)
0.29Real Time Clock is not responding
(RTC chip fail)
0.3CPR handle switch stuck
(StuckCPRhandle)
1.0524V is out of range
(24V)
1.08Battery not connected to the system or completely
depleted
(batteryMissing)
1.09Damaged battery
(batteryShort)
1. Check cables
2. Check junction boards
1. Reboot product
2. Replace MCU, if 0.02 is present, also issue with
PMB charger chip
3. Replace PMB
1. Check CPR handle
2. Check pull cable
3. Check head actuator
1. Power cable issue
2. PMB ciruit error, replace PMB
1. Check cables
2. Replace battery
1. Replace batteries
1.1Unable to communicate with accelerometer
(Accelerometer error)
• Always use ESD protective equipment before opening antistatic bags and servicing electronic parts.
• Do not place unprotected circuit boards on the floor.
NNoottee -- Always ship back circuit boards to Stryker in the same antistatic bags that the new boards were originally shipped in.
The electronic circuits in the product are completely protected from static electricity damage when factory assembled.
Always use adequate static protection when servicing the electronic systems of the product. All service personnel must use
static protection whenever they are touching wires.
Sample antistatic protection equipment includes:
•1 antistatic wrist strap
•1 grounding plug
•1 test lead with a banana plug on one end and an alligator clip on the other end
Make sure that you follow the ESD manufacturer’s instructions for appropriate protection against static discharge.
BBaatttteerryy rreeppllaacceemmeenntt
TToooollss rreeqquuiirreedd::
•5/32” hex driver
•#2 Phillips screwdriver
•3/8” nut driver
PPrroocceedduurree::
1. Raise the product to the highest height position.
2. On the footboard control panel, press EEnntteerr to access the SSeettttiinnggss menu.
3. Highlight SShhuuttddoowwnn and press EEnntteerr.
4. Unplug the power cord from the wall outlet.
5. Push down on the brake pedal to apply the brake.
6. Using a 5/32” hex driver, remove the two screws and flat washers that secure the motion interrupt pan to the litter
weldment. Remove the motion interrupt pan.
7. Using a #2 Phillips screwdriver, remove the two screws from the power supply mounting bracket closest to the center of
the bed.
8. Using a #2 Phillips screwdriver, remove the two screws from the power supply mounting bracket closest to the outside
of the bed.
9. Hinge the batteries down.
10.Unplug the two battery supply cables from the main control board.
11.Unplug the USB cable from the main control board.
12.Using a 3/8” nut driver, remove the nut that secures the ground cable to the battery mounting plate.
13.Lift up to remove the battery mounting plate assembly from the litter.
14.Reverse steps to reinstall.
15.Verify proper operation of the product before you return it to service.
5900-009-002 Rev A.025EN
CCaasstteerr rreeppllaacceemmeenntt
CCAAUUTTIIOONN
• Always perform this procedure in a secure location with the floor jack secure to the base frame before you remove the
caster to prevent the risk of injury.
• Do not put your hands or feet below the caster when you remove or attach the caster to prevent the risk of injury.
TToooollss rreeqquuiirreedd::
•#2 Phillips screwdriver
•Small flat head screwdriver
•5 mm hex wrench
•Small floor jack
PPrroocceedduurree::
1. On the footboard control panel, press EEnntteerr to access the SSeettttiinnggss menu.
2. Highlight SShhuuttddoowwnn and press EEnntteerr.
3. Unplug the power cord from the wall outlet.
4. Using a small flat head screwdriver, remove and save the four base cover screw caps.
5. Using a #2 Phillips screwdriver, remove and save the four screws that secure the base cover to the base frame.
Remove and save the base cover.
NNoottee -- Set the brakes to the neutral position.
6. Using a small floor jack, raise the base frame high enough to remove the caster.
7. Using a 5 mm hex wrench, remove and save the caster locating screw. Remove and discard the caster.
8. Reverse steps to reinstall.
NNoottee -- The caster stem has a red and green half. Face the red half of the caster stem toward the foot end of the bed.
9. Verify proper operation of the product before you return it to service.
1. Raise the product to the highest height position.
2. On the footboard control panel, press EEnntteerr to access the SSeettttiinnggss menu.
3. Highlight SShhuuttddoowwnn and press EEnntteerr.
4. Unplug the power cord from the wall outlet.
5. Push down on the brake pedal to apply the brake.
6. Using a 5/32” hex driver, remove the two screws and flat washers that secure the motion interrupt pan to the litter
weldment. Remove the motion interrupt pan.
7. Using a #2 Phillips screwdriver, remove the two screws from the power supply mounting bracket closest to the center of
the bed.
EN265900-009-002 Rev A.0
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