Basic American Medical Products, a division of GF Health Products, Inc.www.grahamfield.com999-0831-190A Service Manual
!
Safe
Working
Load
Double
Insulated
Protected
Grounded
Device
Type B
Equipment &
Applied Parts
3
Zenith aps seRies
IMPORTANT SAFETY AND WARNING INFORMATION
This product is a variable height, adjustable mattress
platform, which will provide comfort and convenience
!
for residents/patients and caregivers in long term
care settings.
The MAXIMUM SAFE WORKING LOAD for the
APS 9000 Bed with weight evenly distributed
!
bedding, resident/patient, support surface, and all
accessories, is 600 lbs.
NEVER operate the bed if a Power Cord or Plug is
!
damaged or not working properly. Contact qualified
Service Personnel for examination and repair. Always
unplug the Power Cord when performing any maintenance on the bed.
DO NOT open assemblies such as the Actuators, Hand
Control, or Control Box. If unauthorized personnel
!
perform work on these components, the manufacturer’s
warranty becomes void.
DO NOT use unauthorized parts, accessories, or
!
adaptors other than those specified/authorized by
GF Health Products, Inc.
When operating the High/Low, Knee, or Back Functions
!
of the bed, ALWAYS ensure that the confined individual
is positioned properly within the confines of the bed.
DO NOT let any extremities protrude over the side or
between the bed rails when performing these functions.
DO NOT lower the bed when objects are beneath it.
!
Failure to inspect under the bed can result in damage
to property or personal injury.
The bed’s Pendant Cord MUST BE ROUTED AND
SECURED PROPERLY to ensure it does not become
!
entangled and eventually severed during use. Also
make sure all electrical cords DO NOT get tangled
around the bed, side rails, or legs during transport or
normal operation of the bed.
When using nasal- or masked-type administering
!
equipment, all oxygen or air tubing MUST BE ROUTED
AND SECURED PROPERLY to ensure that the tubing
does not become entangled and eventually severed
during the normal operation of the bed.
, including
The bed should ALWAYS be left in its lowest position
!
when unattended to reduce the risk of injury while getting
in or out of the bed.
Keep all moving parts free of obstructions (i.e. blankets/
!
sheets, heating blankets/pads, wiring, etc.)
DO NOT use the assist devices as push handles for moving
the bed. Assist devices can be deformed or broken if
!
excessive side pressure is exerted. Assist devices are not
meant for patients considered as high risks for entrapment
(i.e. patients with pre-existing conditions such as
confusion, restlessness, lack of muscle control, altered
mental status, either organic or medicinal, or a combination thereof). Additional safety measures should be
considered for such high-risk patients.
NEVER permit more than one (1) person on/in the bed
!
at any time.
Body weight should be evenly distributed over the
sleeping surface of the bed. DO NOT allow the patient
!
to lay, sit, or lean in such a way that their entire body
weight is placed only on the raised head or foot sections
of the bed. This especially applies when repositioning
or transferring a patient in or out of the bed. Increased
risk may occur when the patient’s size and/or weight are
inappropriate for the bed’s dimensions or weight capacity.
The bed is intended for use, storage, and transport within
a temperature range of -40˚C to +60˚C. It has a water-
!
resistance rating of IPX4 and IS NOT
washed or submersed.
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Operation of the bed is based on the following conditions:
Ambient Temperature of +10˚C to +40˚C; Relative Humidity
of 30% to 75% (Non-condensing); Atmospheric Pressure of
700hPa to 1060hPa; and a Splash Protection of IEC 60529.
-(+!
Storage of the bed is based on the following conditions:
Ambient Temperature of -10˚C to 70˚C; Relative Humidity
of 10% to 100%; and an Atmospheric Pressure of 500hPa
to 1060hPa.
#(+*.'1'-+ +'
RFI influences most electronic equipment. Caution should be
exercised with regard to the use of portable communications
equipment in the area around such equipment. If RFI causes
erratic behavior, shut the bed off immediately. Leave it off
while the transmission is in progress.
to be power-
4
Basic American Medical Products, a division of GF Health Products, Inc.www.grahamfield.com999-0831-190A Service Manual
Zenith aps seRies
TYPICAL APS 9000 BED IDENTIFICATION LABELS
with Grounded Electrical Cable
ETL
Logo
DUTY CYCLE - 2 min Continuous/18 min
MODE OF OPERATION - Intermittent
APS98174
MODEL NO. 806-0000-000000MFG DATE 12/23/11
GF HEALTH
PRODUCTS, INC.
600 lbs
=
SAFE WORKING LOAD
!
SERIALAPS 9
SERIAL APS98174
IPX4
ZENITH 806 SERIES
PATENT PENDING
APS9000
TYPICAL APS 9000 BED IDENTIFICATION LABELS
MODEL NO
806-0000-000000
MFG. DATE
12/23/11
VOLT HZ AMP TYPE
110-120 50/60 4.5 AC
SERIAL NO
000000000000
SERIAL APS 9
000000000000
for Class II Models
Bed labels are an important part of
identifying your bed’s make and model
when ordering replacement parts. The
Serial Number is essential if you are
claiming parts or service under warranty.
These helpful labels can be located on
the main frame rails, immediately below
the sleep decks on either side of the bed.
Please have this IMPORTANT information ready when calling our customer
service or technical support staff at
800-365-2338; it will allow us to better
assist you and quickly answer your
questions and concerns.
ETL
Logo
DUTY CYCLE - 2 min Continuous/18 min
MODE OF OPERATION - Intermittent
APS98174
MODEL NO. 806-0000-000000MFG DATE 12/23/11
GF HEALTH
PRODUCTS, INC.
600 lbs
=
SAFE WORKING LOAD
!
SERIALAPS 9
SERIAL APS98174
IPX4
ZENITH 806 SERIES
PATENT PENDING
APS9000
MODEL NO
806-0000-000000
MFG. DATE
12/23/11
VOLT HZ AMP TYPE
110-120 50/60 4.5 AC
SERIAL NO
000000000000
SERIAL APS 9
000000000000
If you opted for an electrical system without
grounding on your electrical cord, your bed
is designated as a Class II.
The Identification bed labels to the left
represent the labels for Class II beds.
They can be located on the main frame
rails, immediately below the sleep decks
on either side of the bed.
Please have this IMPORTANT information
ready when calling our customer service
or technical support staff at 800-365-2338.
The labels at left will allow us to better
assist you in answering your questions
and concerns.
5
Basic American Medical Products, a division of GF Health Products, Inc.www.grahamfield.com999-0831-190A Service Manual
Zenith aps seRies
TYPICAL SAFETY/WARNING BED LABELS
The following warning labels have been placed on your bed to help protect you and your bed from
damage. Please do not remove any labels from your bed.
WARNING!
DO NOT LOWER BED WHEN OBJECTS ARE
BENEATH BED. FAILURE TO INSPECT UNDER
BED CAN RESULT IN DAMAGE TO PROPERTY
OR PERSONAL INJURY.
ATTENTION:
S’assurer de ne pas faire descendre le lit
lorsque des objets se trouvent sous le lit. Ne
pas inspecter le dessous du lit pourrait entrainer
des dommages materiels et des risques de
blessures.
WARNING!
DO NOT LOWER BED WHEN
OBJECTS ARE BENEATH BED.
FAILURE TO INSPECT UNDER
BED CAN RESULT IN DAMAGE
TO PROPERTY OR PERSONAL
INJURY.
CAUTION
THIS BED IS SUITABLE FOR USE ONLY WITH
OXYGEN ADMINISTERING EQUIPMENT OF
THE NASAL OR MASK TYPE OR A TENT
COVERING ONLY THE UPPER HALF (HEAD
END) OF THE BED. OXYGEN TENT CANOPIES
SHOULD NOT EXTEND BELOW BED SPRING
LEVEL. LOCK HAND CONTROL AT FOOT OF
BED WHEN USING OXYGEN ADMINISTERING
EQUIPMENT.
ATTENTION:
CE LIT PEUT ETRE UTILISE UNIQUEMENT
AVEC UN EQUIPMENT DESTINE A
L’ADMINISTRATION D’OXYGENE DE TYPE
NASAL OU MASQUE OU AVEC UNE TENTE
RECOUVRANT SEULEMENT LA MOTTIE
AVENT (TETE) DU LIT. LES COTES DE LAS
TENTE OXYGENE NE DOIVENT PAS SE
PROLONGER PLUS DAS QUE LA SOMMIER
DU LIT.
6
Basic American Medical Products, a division of GF Health Products, Inc.www.grahamfield.com999-0831-190A Service Manual
Zenith aps seRies
ENTRAPMENT & COMPLIANCE INFORMATION
On March 10, 2006, the FDA (U.S. Food and Drug Administration) released long-awaited guidelines for reducing the risk
of bed entrapment: “Hospital Bed System Dimensional andAssessment Guidance to Reduce Entrapment”. The new Guidance
identifies potential entrapment areas and those body parts most
at risk for entrapment; provides design criteria for manufacturers
of new hospital/convalescent beds; recommends particular test
methods to assess the conformance of existing hospital/convalescent bed systems; and answers frequently-asked questions
about entrapment issues.
The new Guidance was a result of a long-standing collaboration
between the FDA and the Hospital Bed Safety Workgroup(HBSW), formed in 1999. GF Health Products, Inc’s LongTerm Care Bed division: Basic American Medical Products, is
an HBSW charter member. As a result of our commitment to
product safety, %%(.+.++'-%('!-+&+,"/',-+#-%1-,-'(' (+&-(-"'0.#'.
The guidelines set forth by the FDA Guidance layout specific
dimensional limitations on potentially injury-threatening gaps
and spaces that can occur between bed system components,
such as rails, when not properly installed. GF Health Products,
Inc. and Basic American Medical Products have conformed
to these guidelines from a manufacturing aspect. However,
entrapment issues can often arise when a healthcare provider/
facility has not correctly assembled the components on a bed.
It is essential that the provider/facility fully understand their
responsibility in complying to the guidelines set forth by the
FDA in order to avoid injury. To that end, we have provided
the FDA’s web address at right as a resource for understanding
and following these guidelines for the safety of patients/residents.
It is also essential to have the correct bed components/accessories that correspond with the needs of your patient/resident
and the particular bed you have purchased. Matching the correct
bed component that correlates with the regulatory guidelines can
be a daunting task. Our sales team at GF Health Products, Inc.
and our friendly Customer Service Representatives at Basic
American Medical Products can help you sift through the wide
array of compliance and bed options. We will help you determine
which bed/bed part is best for your patient’s/resident’s particular
needs and help you with your compliance issues.
The APS 9000 bed features a Nurse/Staff Controller in the footboard, however the board is ordered separately with your
bed because of the variety of board styles available. If ordered at the same time as the bed, the Staff Control Assembly
and Shroud Cover will be pre-installed to the Footboard at the manufacturing factory.
STEP 2 - CONNECTING YOUR CABLES
Please refer to DETAIL A shown below.
a. If the Staff Control Assembly is not installed at the
factory you will need to first attach it to the footboard.
b. With the cutout side of the footboard facing outward
as shown, insert the staff control cable through the
large round hole.
c. With text right-side-up, insert the staff control
assembly into the cutout slot on the footboard
and attach to the board using the two outside
small holes and two screws from your staff
control hardware kit.
d. Attach the Shroud Cover over the cable on the
inside of the board using the four remaining
screws from your kit.
e. Insert the T-Cable end (extending out the
foot end with phone jack) into the round
plug, making sure the phone jack is
seated correctly inside the female plug
(arrow to arrow - see DETAIL B.)
f. Screw on the round lock cap onto
the Staff control’s female plug to
secure (see DETAIL B).
SEE PAGE 10 OF THIS
Loop Male Staff Control Cable
and cable tie through mounting
tube hole with Female Staff
Control Cable.
MANUAL FOR PROPER
ASSEMBLY OF ELBOW
MOUNTING BRACKETS
(TUBES) & FOOTBOARD
g. IMPORTANT
Make sure to tie
off the staff control
cable to the footboard mounting
tube with a cable
tie as shown.
DETAIL A
CLOSEUP OF STAFF
CONTROL CABLE CONNECTION
Basic American Medical Products, a division of GF Health Products, Inc.www.grahamfield.com999-0831-190A Service Manual
:
DETAIL B
:
MAKE SURE LOCK
END CAPS ARE
SCREWED ON
SECURELY
:
11
STANDARD MATTRESS RETAINER INSTALLATION
STEP 1. HEAD RETAINER INSTALLATION
1. Position retainer with curved end toward headboard.
2. Squeeze ends of the retainer toward the inside of
the bed and lower between the deck rails and first
outside grid wires.
3. Align the ends of retainer with small holes on the
inside of deck rails and slowly release.
Zenith aps seRies
STEP 2. FOOT-END RETAINER
INSTALLATION
STEP 3. RETAINER POSITIONS
• FOR 80” BEDS: Use outside small holes.
See sample at right.
• FOR 76” BEDS: Use inside small holes.
See sample at right.
1. Position retainer with curved end toward footboard.
2. Squeeze ends of the retainer toward the inside of
the bed and lower between the deck rails and first
outside grid wires.
3. Align the ends of retainer with small holes on the
inside of deck rails and slowly release.
Be sure to use a mattress that is properly sized to fit
!
the sleep deck, which will remain centered on the
deck relative to State and Federal Guidelines. Use
of an improperly fitted mattress could result in injury
or death.
Basic American Medical Products, a division of GF Health Products, Inc.www.grahamfield.com999-0831-190A Service Manual
Use a properly sized mattress in order to minimize
!
the gap between the side of the mattress and assist
devices. This gap must be small enough to prevent
resident/patient from getting his/her head or neck
caught in this location.
12
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