GF13702-INS-LAB-RevA10
1
GF13702: ADVANCED PATIENT ALARM
SETUP & OPERATION INSTRUCTIONS
PLEASE SAVE THESE
INSTRUCTIONS FOR FUTURE USE
GF13702-INS-LAB-RevA10
2
CAUTION: Seat cushions, sling seats, and other environmental fac-
tors may negatively affect alarm operation.
ALARM SETUP
Fig. B
Fig. A
Fig. C
Fig. D
Delay
Switch
Volume
Switch
Low
Battery
Indicator
Advanced Patient Alarm Monitor
AC Adapter
Jack
Sensor Mat
Jack
Battery
Compartment
Strain
Relief
Nurse Call
Button
Reset
Button
Monitor
Positioning
Clip
1. Remove the screw that holds the battery compartment cover in place.
2. Inside the battery compartment (see Fig. B):
a. Set the volume switch to LO, HI, or RE (remote) volume. For de-
scription of the remote alarm feature, see next page.
b. Set the delay switch to either 0 or 2 seconds. Selecting 2-second
alarm delay may reduce the likelihood of false alarms when used
with restless patients.
c. Install a new 9V alkaline battery (not included).
d. Replace battery compartment cover and reinstall screw.
Alarm Testing
WARNING: Test alarm before each use.
1. Insert the sensor pad’s telephone-style plug into the monitor’s sensor
mat jack (see Fig. C) until it clicks into place.
2. To protect the cable plug end from accidental pull force, route the
cable through the strain relief (see Fig. C).
3. Use your hand to apply pressure to the sensor pad. The monitor will
automatically sense the pressure and beep when activated.
4. Remove the pressure and the alarm will sound. To silence the alarm,
press the reset button on the side of the monitor (see Fig. D).
Patient Setup
1. Follow this procedure before each use.
a. If using a chair sensor pad, center the chair sensor pad under the
patient’s buttocks.
b. If using a bed sensor pad, center the bed sensor pad under the
patient’s buttocks.
Note: The most current version of these instructions can be found online
at
www.grahamfield.com
IMPORTANT SAFETY INFORMATION: PLEASE READ
WARNING: Important! Read and understand these instructions
before installing or using the GF13702 Advanced Patient Alarm.
If you do not understand any part of these instructions, contact
a healthcare professional for direction in the use of this product.
If the patient alarm is not properly set up and adjusted, personal
injury and/or damage to the patient alarm could result.
WARNING: If components are damaged or missing, contact
your dealer immediately. DO NOT use substitute parts. Use only
Lumex
®
replacement parts. Non-Lumex
®
replacement parts
could cause personal injury and/or damage to patient alarm.
WARNING: GF Health Products, Inc. assumes no responsibility
for any damage or injury caused by improper assembly or use of
this product.
UNPACKING
Check for any obvious damage to the carton or its contents. If damage is
evident, DO NOT USE. Contact carrier / distributor for further instruction.
INTENDED USE
The intended use of the GF13702 Advanced Patient Alarm is to alert care-
givers when a patient attempts to exit a wheelchair, chair or bed without
assistance. Removal of pressure from the sensor pad beneath the patient
activates the alarm.
Contraindications
WARNING: This device is not a substitute for routine visual
monitoring by caregiver, and is intended to be used in conjunc-
tion with a comprehensive fall management program.
WARNING: No claim is made that this device will prevent patient
falling or reduce the likelihood of injury as a result. The care-
giver is responsible for ensuring that this product is properly
installed, tested, and functioning before each use.
CAUTION: This device is not suitable for all patients, including but
not limited to, those wishing to defeat the alarm system.
CAUTION: This product is designed for individuals weighing 74 lb
or more.