Kisses®
Tag U
ser S
heet
Par
t Number
:
© 2017 ST
ANLEY Healthcar
e.
All Rights Reserved.
07/2017.
0980-324-000 Rev
A.
KB# 10098
ST
ANLEY Healthcare
Lincoln, NE 68503
www
.stanleyhealthcare.com
Phone: +1-800-824-2996
Email: [email protected]
806A9801
Warranty
Kisses Tags are warranted to be free of manufacturing
defects and perform according to the published
specifications at the time they are put in service as
set out in the operating instructions. Because Kisses
Tags are battery powered, NO SPECIFIC LIFE
IS GUARANTEED. Stanley is not responsible for
warranty service should the Kisses label or logo or the
serial number be removed or should the Kisses Tag fail
to be properly maintained or fail to function properly
as a result of misuse, abuse, neglect, improper shipping
or any premature exposure of the tag to light other
than removal from the packaging with the intent of
activating the tag.
Limitation of Liability
This Product has been designed for use to assist in the
prevention of mother/infant mismatching incidents.
The range, accuracy, function and performance of this
Product 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, inter-
ference from other electrical devices, atmospheric effects,
installation, and maintenance. There may be other
factors, which also affect performance of this Product.
STANLEY Healthcare does not guarantee that this
Product will detect 100% of mother/infant matches or
mismatch incidents, nor does STANLEY Healthcare
guarantee that this Product will be free from returning
false reports of mother/infant matches or mismatch
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 detecting 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 mother/infant matches or mismatch incidents.
The failure to undertake regular testing and maintenance
will increase the risk of false reports of mother/infant
matches or mismatch incidents.
STANLEY Healthcare hereby disclaims all warranties,
express or implied, arising out of or in connection
with any of its Products or services, the use of 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.
STANLEY Healthcare’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
STANLEY Healthcare’s Product, defective products
or materials, improper installation or maintenance
of STANLEY Healthcare’s Product or products or the
system in which they are incorporated, or alleged to
have resulted from an act or omission of STANLEY
Healthcare or any person, negligent or otherwise,
shall be limited to the following, at STANLEY
Healthcare’s sole option:
1) the repair or replacement of defective Product
or materials supplied by STANLEY Healthcare
during the warranty period as set out in the
Product documentation; or, at the option of
STANLEY Healthcare,
2) a refund of the purchase price of the Product
supplied by STANLEY Healthcare.
In no event shall STANLEY Healthcare 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 STANLEY
Healthcare, 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.
Operation 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 environ-
ment. 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 cor-
rect the interference at his own expense.
Warning
: Changes or modifications not expressly approved
by STANLEY Healthcare could void the user’s authority
to operate the equipment.
Canada—Industry Canada
This device complies with RSS-310 of Industry Canada.
Operation is subject to the condition that this device does
not cause harmful interference.
European Union
The following statement applies to the Kisses Tag.
CE declaration
STANLEY Healthcare hereby declares that this radio fre-
quency device is in compliance with the essential require-
ments and other relevant provisions of the following EU
directives:
•
RTTE Directive 1999/5/EC
•
CE mark Directive 2004/108/CE
•
LVD 2006/95/EC
Pat. US 6977586, CA 2436798, WO/2002/065421
Conforms to
UL STD 294
