Xmark Corporation IPSR Benutzerhandbuch

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

Off

Normal operation.

Flashing

every 0.5 sec.

Unconfigured Receiver. Run Auto

Configure using the PS System Man-

ager.

Failure. Check power supply to the

device. Download Neuron firmware

to the Receiver using the PS System

Manager.

Momentarily

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