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To protect the environment, dispose of
empty batteries at appropriate collec-
tion sites according to national or local
regulations.
Calibration
The thermometer is initially calibrated at the
time of manufacture. If this thermometer is used
according to the use instructions, periodic re-
adjustment is not required. If at any time you
question the accuracy of temperature measure-
ments, please contact Kaz Customer Service
at 1-800-327-7226.
Manufacturing date is given by the LOT number
located in the battery compartment. The first
number after LOT represents the last digit of the
year of manufacture.
The last two digits give the week of manufacture.
An example: LOT 503 – this product has been
manufactured in week 03 of the year 2005.
Product specifications
Displayed temperature range: 93.2 °F 108 °F
(34 °C 42.2 °C)
Operating ambient
temperature range: 50 °F 104 °F
(10 °C 40 °C)
Display resolution: 0.1 °F or °C
Accuracy for patient
Maximum Laboratory
temperature range
Error
96.8 °F 102.2 °F
(36 °C 39 °C): ± 0.4 °F (± 0.2 °C)
outside this range: ± 0.5 °F (± 0.3 °C)
Long term storage ranges
Temperature: –4 °F to 122 °F
(–20 °C to 50 °C)
Humidity: 95 % non-
condensing
Battery life: 2 years / 1000
measurements
If device is not used within specified temperature
and humidity ranges the technical accuracy can
not be ensured.
This infrared thermometer meets requirements
established in ASTM Standard E 1965-98 (for the
thermometer system [thermometer with lens filter]).
Full responsibility for the conformance of the
product to the standard is assumed by
Kaz, Inc., Hudson, NY 12534 USA.
ASTM laboratory accuracy requirements for the
thermometer only (not including a lens filter) in
the display range of 96.8 °F to 102.2 °F (36 °C
to 39 °C) for infrared thermometers is ± 0.4 °F
(± 0.2 °C), whereas for mercury-in-glass and
electronic thermometers, the requirement per
ASTM Standards E 667-86 and E 1112-86 is
± 0.2 °F (± 0.1 °C).
This appliance conforms to the following
standards:
DIN EN 60601-1: 3/96 «Medical electrical
equipment» – Part 1: General requirements for
safety
DIN EN 60601-1-2/2001 «Medical electrical
equipment» – Part 1-2: General requirements for safety
– collateral standard: Electromagnetic compatibility –
requirements and tests
DIN EN 12470-5: 2003 «Clinical thermometers» –
Part 5: Performance of infrared ear thermometers
(with maximum device)
6026360_KAZ_IRT3020 Seite 7 Montag, 13. August 2007 1:16 13
7


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