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
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.
4
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.com6300, 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.
5
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.
6
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
7
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