8
Product specifications
Displayed temperature range: 34 – 42.2 °C (93.2 – 108 °F)
Operating ambient temperature range: 10 – 40 °C (50 – 104 °F)
Storage temperature range: -25 – 55 °C (-13 – 131 °F)
Operating relative humidity: 10-95% RH (noncondensing)
Storage relative humidity: 15-95% RH (noncondensing)
Display resolution: 0.1 °C or °F
Accuracy for displayed temperature range Maximum Laboratory Error
35 – 42 °C (95 – 107.6 °F): ±0.2 °C (±0.4 °F)
Outside this range: ±0.3 °C (±0.5 °F)
Clinical repeatability: ±0.14 °C (±0.26 °F)
Battery Type: 2 X 1.5V type AA (LR 06) batteries
Battery life: 2 years/350 measurements/ 100 minutes in nightmode
Service life: 5 years
Accessory: Lens filter, LF40/LF20, single use
The measured temperature is converted to an oral equivalent value.
This thermometer is specified to operate at 1 atmospheric pressure or at altitudes with an atmospheric pressure
up to 1 atmospheric pressure (700 - 1060 hPa).
10 °C
40 °C
10
Equipment with
type BF applied parts
See Instruction for use Operating temperature Storage temperature Operating humidity Storage humidity
LOT SN REF MD
Caution Batch code Serial number Catalogue number Medical device Lens lter: Do not re-use
Manufacturer Date of manufacture Keep it dry
Subject to change without notice.
This medical device carries the CE mark and is manufactured in conformity with RoHS Directive 2011/65/EU and other
applicable directive and/or regulations as specified in the EU Declaration of Conformity. Full responsibility for the
conformance of the product to the standard is assumed by Kaz Europe Sarl, Place Chauderon 18, CH-1003 Lausanne,
Switzerland.
ASTM laboratory accuracy requirements in the display range of 37 to 39 °C (98 to 102 °F) for IR thermometers is ±0.2 °C
(±0.4 °F), whereas for mercury-in-glass and electronic thermometers, the requirement per ASTM Standards E667-86 and
E1112-86 is ±0.1 °C (±0.2 °F).
MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC. NOTE: Do not use this device in the
presence of electromagnetic or other interference outside the normal range specified in EN 60601-1-2. For detailed
description of EMC requirements please visit website (Support / Document center) or contact service center.
Portable and mobile RF communications equipment can aect MEDICAL ELECTRICAL EQUIPMENT.
This product contains batteries and recyclable electronic waste. To protect the environment, do not dispose of
it in the household waste, but take it to appropriate local collection points.
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 the temperature
measurement, please contact your authorized service center.
Manufacturing date is given by the LOT number located in the battery compartment.
The first three (3) digits after LOT represent the Julian date that the product was manufactured and the next two (2)
digits represent the last two numbers of the calendar year the product was manufactured. The last identifiers are the
letters that represent the manufacturer.
An example: LOT 11614K, this product has been manufactured on the 116th day of the year 2014.
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