User's Manual
Service Light
The red service light is located on the lower side of the Receiver,
next to the service pin, and is used for troubleshooting.
Red Service
LED state
Description
O Normal operation.
Flashing
every 0.5 sec.
Uncongured Receiver. Run Auto
Congure using the PS System Man-
ager.
On Failure. Check power supply to the
device. Download Neuron rmware
to the Receiver using the PS System
Manager.
Momentarily
on
Service pin pressed.
Warranty
Stanley Healthcare Solutions’ products are warranted against
defects in materials and workmanship and shall perform in
accordance with published specifications for a period of one
year. Stanley Healthcare Solutions’ warranty is limited solely
to the repair or replacement of the defective part or product.
Stanley Healthcare Solutions reserves the right to change
product specifications without notice.
Limitation of Liability
This Product has been designed for use to assist in the preven-
tion of patient abduction and/or wandering incidents.
The range, accuracy, function and performance of this Prod-
uct may vary from the published specifications due to many
factors, including, but not limited to, site impairments from
structural effects, metal objects in the vicinity, placement of
the receiver and transmitter, interference from other electrical
devices, atmospheric effects, installation, and maintenance.
There may be other factors, which also affect performance of
this Product.
XMARK Corporation (“XMARK”) does not guarantee that
this Product will detect 100% of patient abductions and/or
wandering incidents, nor does XMARK guarantee that this
Product will not return false reports of calls for patient abduc-
tions and/or wandering incidents.
Monthly testing and maintenance of this Product, as described
in the Product documentation, is essential to verify the system is
operating correctly and to ensure that the probability of detect-
ing an alarm and/or locating the transmitter are maximized.
The failure to undertake regular testing and maintenance will
increase the risk of system failure and failure to detect patient
abductions and/or wandering incidents. The failure to under-
take regular testing and maintenance will increase the risk of
false reports of patient abductions and/or wandering incidents.
XMARK hereby disclaims all warranties, express or implied,
arising out of or in connection with any of its Products of
the use or performance thereof, including but not limited
to, where allowable by law, all other implied warranties
or conditions of merchantability, fitness for a particular
purpose, and those arising by statute or otherwise in law
or from a course of dealing or usage of trade.
XMARK’s liability to you or anyone claiming through or on
behalf of you with respect to any claim or loss arising out
of the use or misuse of XMARK’s Product, defective prod-
ucts or materials, improper installation or maintenance of
XMARK’s Product or products or the system in which they
are incorporated, or alleged to have resulted from an act or
omission of XMARK or any person, negligent or otherwise,
shall be limited to the following, at XMARK’s sole option:
1) the repair or replacement of defective Product or materials
supplied by XMARK during the warranty period as set out
in the Product documentation; or, at the option of XMARK,
2) a refund of the purchase price of the Product supplied by
XMARK.
In no event shall XMARK be liable for general, specific,
indirect, consequential, incidental, exemplary or punitive
damages or any losses or expenses suffered by you or anyone
else, whether or not XMARK, or its employees, officers,
agents, resellers or installers has been informed of the risk
of such loss or expense and whether or not such losses or
expenses were foreseeable.
Statements
United States—Federal Communication Commission (FCC)
This device complies with Part 15 of the FCC Rules. Opera-
tion is subject to the following two conditions: (1) this device
may not cause harmful interference, and (2) this device must
accept any interference received, including interference that
may cause undesired operation.
NOTE: This equipment has been tested and found to comply
with the limits for a Class A digital device, pursuant to Part
15 of the FCC Rules. These limits are designed to provide
reasonable protection against harmful interference when the
equipment is operated in a commercial environment. This
equipment generates, uses, and can radiate radio frequency
energy and, if not installed and used in accordance with the
instruction manual, may cause harmful interference to radio
communications. Operation of this equipment in a residential
area is likely to cause harmful interference in which case the user
will be required to correct the interference at his own expense.
Warning: Changes or modifications not expressly approved by
XMARK could void the user’s authority to operate the equipment.
Canada—Industry Canada
The term “IC:” before the certification/registration number
only signifies that Industry Canada technical specifications
were met.
European Union—CE Declaration
XMARK hereby declares that this radio frequency receiver
is in compliance with the essential requirements and other
relevant provisions of the following EU directives: (1) RTTE
Directive 1999/5/EC, (2) CE mark Directive 2004/108/CE,
and (3) LVD 2006/95/EC.
Patient Security Receiver Installation Guide