A.MENARINI GLUCOFIX TECH User Manual page 7

10. Warranty
Your GLUCOFIX® TECH meter is guaranteed to be free of material and
workmanship defects for 2 years from the date of purchase (except as
noted below). If at any time during the first 2 years after purchase, your
GLUCOFIX® TECH meter does not work for any reason (other than as
described below), it will be replaced with a new meter, or a substantial
equivalent, free of charge. Should you wish to extend the warranty
period for your meter, please refer to the warranty card.
This warranty is subject to the following exceptions and limitations:
● this warranty is only applicable to the original purchaser;
● this warranty does not apply to units which malfunction or are
damaged due to obvious tampering, misuse, alteration, neglect,
unauthorized maintenance or failure to operate meter in accordance
with the Instructions;
● there is no other express warranty for this product. The option of
replacement, described above, is the warrantor's only obligation under
this warranty.
The original purchaser must contact A. Menarini Diagnostics: Telephone
Number XXXXXXXX.
A. Menarini Diagnostics is committed to using your personal information
responsibly and in compliance with the law. You have our pledge that
we will not disclose or sell your personal information with third-parties.
The information you voluntarily provide will be used to help us serve
you better in the future.
11. Symbols and abbreviations
Consult instructions for use
Caution, consult instructions for use
Temperature limitation
Use by
Manufacturer
Batch code
In vitro diagnostic medical device
In vitro device for self-testing
Serial number
Recyclable package
CE marking
Contamination risk due to the use of blood samples
Blood glucose meter
Significant additions or changes from previous user
manual revision
Direct current (voltage)
Catalogue number
The meter complies with the requirements of directive 2011/65/EU on
the restriction of use of certain hazardous substances in electrical and
electronic equipment and with the requirements of directive 98/79/EC
on in vitro diagnostic medical devices.
7