Stryker BERTEC GOBED PLUS FL20E, GOBED+ Operation Manual

ELECTRIC ACUTE CARE BED
Model FL20E (USA: 2501)
TECHNICAL ASSISTANCE AND PARTS
1 800 428-5025 (Canada) E-mail (Canada only): service@bertec.strykercorp.com 1 800 327-0770 (United States)
Manufactured by Stryker Bertec Medical Inc
72-0439 R1.3 September 2003 F15-43-E-A Printed in Canada
TABLE OF CONTENTS
1. INTRODUCTION................................................................................................................... 4
1.1 Bed Specifications.......................................................................................................... 4
1.2 Technical Support........................................................................................................... 5
1.3 Warning / Caution / Note Definitions............................................................................... 5
1.4 Safety Tips and Guidelines............................................................................................. 5
1.5 Warranty......................................................................................................................... 7
Limited Warranty............................................................................................................ 7
To Obtain Service and/or Parts....................................................................................... 7
Return Authorization....................................................................................................... 7
Damaged Merchandise .................................................................................................. 7
1.6 Symbols ......................................................................................................................... 7
1.7 Set-Up Procedure........................................................................................................... 8
1.8 Cleaning and Preventative Maintenance ........................................................................ 9
Bed Cleaning and Mattress Care.................................................................................... 9
Preventative Maintenance............................................................................................ 10
1.9 Bed Position Pictograms............................................................................................... 11
1.10 Bed Illustration............................................................................................................ 11
2. OPERATION GUIDE........................................................................................................... 12
2.1 Switching On Power..................................................................................................... 12
2.2 Applying the Brakes...................................................................................................... 12
2.3 Moving the bed............................................................................................................. 12
2.4 Foley Bag Hook Usage................................................................................................. 13
2.5 Foot Support Arm Operation......................................................................................... 13
2.6 Patient Restraint Strap Locations ................................................................................. 13
2.7 Emergency CPR Release (Optional) ............................................................................ 14
2.8 Night Light Usage (Optional)......................................................................................... 14
2.9 Nurse Call Usage (Optional)......................................................................................... 14
2.10 Auxiliary Power Outlet Usage (Option Available w/120V~ Bed Model)........................ 14
2.11 Positioning Siderails................................................................................................... 15
2.12 Head and Foot Board Operation................................................................................. 15
2.13 Head Siderail Function Guide..................................................................................... 16
2.14 Foot Board Control Panel Guide................................................................................. 17
2.15 Function Lockout Usage............................................................................................. 17
2.16 Weigh System Control Panel Guide (Optional)........................................................... 18
Operating (Zeroing) the Scale Before Putting a New Patient on the Bed...................... 18
Adding or Removing Equipment when a Patient is on the Bed..................................... 19
Changing Manually the Numerical Value of Displayed Weight...................................... 19
Changing the Weight Measure Unit.............................................................................. 19
2.17 Chaperone Bed Exit (Optional)................................................................................... 20
2.18 Chaperone Bed Exit with Zone Control (Optional) ...................................................... 21
Zone Settings................................................................................................................ 21
3. ACCESSORIES.................................................................................................................. 22
GOBED+ Operations Manual
1. INTRODUCTION
This manual is designed to assist you with the operation of the Model FL20E . Read it thoroughly before operating the bed. Hospital staff should be able to refer to this manual at all time when using the bed. This Operations Manual is an integral part of the bed and should be included if the bed is sold or transferred.
1.1 BED SPECIFICATIONS *
Safe Working Load 579 lb (263 kg) Weigh System Capacity Patients weighing up to 500 lb (227 kg) Weigh System Accuracy ± 2 % of patient weight from 100 lb (45.3 kg) to 500 lb
(227 kg) ± 2 lb of patient weight under 100 lb (45.3 kg)
Overall Length/Width 92 7/8" x 42 9/16" (235 cm x 108.1 cm) - siderails up
92 7/8" x 38 3/4" (235 cm x 98.4 cm) - siderails down Weight w/Boards 417 lb (189 kg) Patient Sleep Surface 35 x 80" (89 x 203 cm) extendable to 82" (208 cm) &
84" (213 cm) Recommended Mattress Size 35 x 80" (89 x 203 cm); 35 x 82" (89 x 208 cm); 35 x
84" (89 x 213 cm); 6.25" (15.9 cm) max. thickness Min/Max Mattress Support Height: 14.5 to 28.9" (36.8 to 73.4 cm) Fowler Angle w/CPR Mechanism
Fowler Angle w/o CPR Mechanism Knee Gatch Angle w/o Auto Contour
Knee Gatch Angle w/Auto Contour
0 to 60°
0 to 65°
0 to 32°
0 to 24° Trendelenburg/Reverse Trendelenburg +14 to -14° Environmental Conditions
- Transport and storage
- Ambient Temperature
- Relative humidity
- Atmospheric Pressure
- Operating **
- Ambient Temperature
- Relative humidity
- Atmospheric Pressure Electrical Requirements - all electrical
requirements meet CSA C22.2 No. 601.1­M90, UL 2601 and IEC 60601-1, 60601-2­38 specifications.
-40 to 70°C (-40 to 158°F)
10 to 100%
500 to 1060 hPa
18.3 to 26.7°C (65 to 80°F)
20 to 80% without condensation
700 to 1060 hPa
100V, 50-60Hz, 7.5A -Two 250V, 10A Slow Blow
Fuses
120V, 50-60Hz, 4.0A -Two 250V, 10A Slow Blow
Fuses
120 V, 50-60Hz, 9.8A w/Auxiliary Outlet - Two 250V,
10A Slow Blow Fuses
200V, 50-60Hz, 3.2A -Two 250V, 6.3A Slow Blow
Fuses
220V, 50-60Hz, 2.9A -Two 250V, 6.3A Slow Blow
Fuses
240V, 50-60Hz, 2.7A -Two 250V, 6.3A Slow Blow
Fuses
* Stryker Bertec pays special attention to product improvement and reserves the right to change specifications without notice.
**Operating environment recommended to ensure the scale precision.
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Introduction Chapter 1
WWAARRNNIINNGG
WWAARRNNIINNGG
1.2 TECHNICAL SUPPORT
For questions regarding this product, contact the following Technical Service department or your local representative:
In Canada: In the United States: Stryker Bertec Medical Inc Stryker Medical
1 800 428-5025 1 800 327-0770 E-mail (Canada only):service@bertec.strykercorp.com 6300, South Sprinkle Road 70, 5th Avenue, P.O. Box 128 Kalamazoo, MI 49001-9799 L’Islet (Québec), G0R 2C0, Canada USA
1.3 WARNING / CAUTION / NOTE DEFINITIONS
The words WARNING, CAUTION and NOTE carry special meanings and should be carefully reviewed.
The personal safety of the patient or user may be involved. Disregarding this information could result in injury to the patient or user.
CCAAUUTTIIOON
N
These instructions point out special procedures or precautions that must be followed to avoid damaging the equipment.
E
NNOOTTE
Notes provide special information to make maintenance easier or important instructions clearer.
1.4 SAFETY TIPS AND GUIDELINES
Before operating the , it is important to read and understand all information in this manual. Carefully read and strictly follow the safety guidelines listed below.
It is important that all users have been trained and educated on the inherent hazards associated with the usage of electric beds.
The is not intended for pediatric use.
The mattress thickness should not exceed 6.25" (15.9 cm).
This bed is equipped with a hospital grade plug for protection against shock hazard. It must be
plugged directly into a properly grounded receptacle. Grounding reliability can be achieved only when a hospital grade receptacle is used.
Serious injury can result if caution is not used when operating the bed. Operate the bed only when all people and equipment are clear of the electrical and mechanical systems.
Always apply the brakes when a patient is on the bed (except during transport). Serious injury could result if the bed moves while a patient is getting on or off the bed. After the brake pedal is engaged, push on the bed to ensure the brakes are securely locked.
To help reduce the number and severity of falls by patients, always leave the bed in the lowest position when the patient is unattended.
Leave the siderails fully up and locked when the patient is unattended. When raising the siderails, be sure that you hear the click that signals the up and locked condition. Pull firmly on the siderail to ensure it is locked into position.
Keep siderails in the fully raised position and the sleep surface horizontal in its lowest position when the patient is sleeping unless the patient's medical conditions dictates otherwise.
When the sleep surface sections are articulated, ensure that all patient's extremities are within the raised siderails to avoid patient injury.
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GOBED+ Operations Manual
Siderails, with or without their padded covers or nets, are not intended to serve as restraint devices to keep patient from exiting the bed. Siderails are designed to keep a patient from inadvertently rolling off the bed. It is the responsibility of the attending medical personnel to determine the degree of restraint necessary to ensure a patient will remain safely in bed. Failure to utilize the siderails properly could result in serious patient injury.
To reduce risk of injury, ensure the sleep surface is horizontal and in the lowest position with the siderails fully raised and locked when moving the bed with a patient in it.
To avoid injury to the patient and/or user, do not attempt to move the bed laterally with the steer pedal engaged. The fifth steer wheel cannot swivel.
When a patient's condition requires greater safety measures for his/her security, use the lockout switches in the foot board control panel to inhibit the siderail functions or remove any optional pendant control and install protective pads on the siderails.
The instant CPR release is for emergency use only. When activating the CPR release handle, all people and equipment must be removed from the area below and around the head, thigh and foot sections of the bed or serious personal injury or equipment damage could occur.
Possible fire hazard exists when this bed is used with oxygen administering equipment other than nasal, mask type or half bed-length tent type. It is recommended to unplug the bed power cord from the wall when oxygen-administering equipment is used. When using a half bed-length tent type, ensure the siderails are outside the oxygen tent and oxygen tent should not extend below the mattress support level.
The Weigh system is intended to assist in the monitoring of the patient's weight variation. Under no circumstances should its reading be used as sole reference for medical treatment.
The Bed Exit system is intended only to aid in the detection of a patient exiting the bed. It is not intended to replace patient monitoring protocol. The Bed Exit system signals when a patient is about to exit the bed. Adding or removing objects from the bed after having armed the Bed Exit system may cause a reduction in the sensitivity of the Bed Exit system, resulting in erroneous readings of the patient's movements in the bed.
The Bed Exit system is not designed to be used with patients weighing less than 50 lb (23 kg).
When large fluid spills occur in the area of the circuit board, cables and motors, immediately
unplug the bed power cord from the wall outlet. Remove the patient from the bed and clean up the fluid. Have maintenance completely check the bed. Fluids can have an adverse effect on operational capabilities of any electrical product. DO NOT put the bed back into service until it is completely dried and has been thoroughly tested for safe operation.
Do not steam clean, hose off or ultrasonically clean the bed. Do not immerse any part of the bed. The internal electrical parts may be damaged by exposure to water. Hand wash regularly all surfaces of the bed with warm water and a mild detergent. Wipe cleaned surfaces dry to avoid build up of cleaning substance. Inspect the mattress after each use. Discontinue use if any cracks or rips are found in the mattress cover, which may allow fluid to enter the mattress. Failure to properly clean the mattress, or dispose of it if defective, may increase the risk of exposure to pathogenic substances and may bring about diseases to the patient and user.
Preventive maintenance should be performed at least once a year to ensure all bed features are functioning properly. Ensure that any bed malfunction is promptly reported to service personnel for immediate attention.
Always unplug the bed power cord from the wall outlet when servicing or cleaning the bed. When working under the bed with the bed in the high position, always place blocks under the mattress support frame and apply the brakes to prevent injury in case the Bed Down switch is accidentally pressed.
To avoid damage to the siderail mechanisms, do not move the bed using the raised siderails. Use the push/pull handles integrated to the boards to move the bed.
Before using the optional manual crank during a power failure, always unplug the power cord. An unexpected return of power could rotate the handle and cause injury.
When servicing use only identical replacement parts provided by Stryker Bertec.
NOTE
Throughout this operations manual, the words “right” and “left” refer to the right and left sides of a patient lying face up on the bed.
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Introduction Chapter 1
electric
systems
electric systems
1.5 WARRANTY
LIMITED WARRANTY
All Stryker Bertec products are guaranteed against material or manufacturing defects, improper operation of mechanisms, and premature wear of bed components under normal use conditions.
For questions regarding warranty, please contact Stryker Bertec Technical Service department (see section 1.2) or your local representative.
TO OBTAIN SERVICE AND/OR PARTS
For an on-site diagnosis of a malfunction a Field Service Representatives or to order replacement parts, simply contact our Service department (see section 1.2) or your local representative. For the part ordering procedure, refer to section 1.5 of the bed maintenance manual, “To Obtain Service and/or Parts”.
RETURN AUTHORIZATION
Merchandise cannot be returned without approval from the Stryker Bertec Technical Service department. An authorization number will be provided, which must be clearly printed on the returned merchandise. Stryker Bertec reserves the right to charge shipping and restocking fees on returned items.
DAMAGED MERCHANDISE
Claims for damaged merchandise must be made with the carrier within fifteen (15) days of receipt of merchandise. DO NOT ACCEPT DAMAGED SHIPMENTS UNLESS SUCH DAMAGE IS NOTED ON THE DELIVERY RECEIPT AT THE TIME OF RECEIPT. Upon prompt notification, Stryker Bertec will file a freight claim with the appropriate carrier for damages incurred. Claims will be limited in amount to the actual replacement cost. In the event that this information is not received by Stryker Bertec within the fifteen (15) day period following the delivery of the merchandise, or the damage was not noted on the delivery notice at the time of receipt, the customer will be responsible for payment of the original invoice in full.
Claims for any short shipment must be made within 5 days of invoice.
1.6 SYMBOLS
Warning, consult accompanying documents
Fuse rating for bed with the 100V and 120V
10A 125V
Fuse rating for beds with 200V∼, 220V∼ and 240V∼
6.3A 250V
Protective earth (ground)
Alternating Current
Type B Equipment
IPX4 Protection from liquid splash
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