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Product speci cations
Type: No touch + forehead thermometer (NTF 3000)
Measuring range: 34.4 °C – 42.2 °C (93.9 °F – 108 °F)
Resolution: 0.1 °C (0.1 °F)
Laboratory Accuracy: ±0.2 °C for the range 35 °C – 42 °C (±0.4 °F for 95 °F – 107.6 °F)
±0.3 °C (outside this temperature range)
(Ambient Temperature: 15 °C to 40 °C (59 °F to 104 °F))
Display: Liquid Crystal Display, 4 digits plus special icons
Acoustic: Audio:
Normal temp range = single long beep for 2 sec duration
Fever = Red or Yellow temp range: 10 short beeps
Operating temperature: 15 °C – 40 °C (59 °F to 104 °F)
Automatic Switch-o : Approx. 60 seconds after last measurement has been taken
Weight: 99.5 g (with batteries), 77.1 g (w/o batteries)
Long term storage ranges
Storage/transport temperature: -25 °C to 60 °C (-13 °F – 140 °F)
Humidity: 15–95% non-condensing
Battery: (2) AA Batteries - at least 1000 measurements
Pressure: 700-1060 hPA (0,7-1,06 atm)
This product conforms with the provisions of the European directive 93/42/EEC (Medical Device
Directive). This infrared thermometer meets requirements established in ASTM Standard E 1965-98 for the
thermometer system. Full responsibility for the conformance of the product to the standard is assumed by
Kaz Europe Sàrl, Place Chauderon 18, CH-1003 Lausanne, Switzerland.
ASTM laboratory accuracy requirements for the thermometer only in the display range of 36 °C to 39°C
(96.8 °F to 102.2 °F) for infrared thermometers is ±0.3 °C (±0.5 °F), whereas for mercury-in-glass and
electronic thermometers, the requirement per ASTM Standards E 667-86 and E 1112-86 is ±0.1 °C (±0.2 °F).
This device conforms to the following standards:
EN 60601-1:2006 Medical electrical equipment. General requirements for basic safety and
essential performance
EN 80601-2-56 Particular requirements for basic safety and essential performance of clinical
thermometers for body temperature measurement
ASTM 1965E – ASTM Standard for Infrared Clinical Thermometers
EN 12470-5: 2003 «Clinical thermometers» – Part 5: Performance of infrared ear thermometers (with
maximum device)
EN 60601-1-2: Medical electrical equipment – Part 1-2: General requirements for basic safety and essential
performance – Collateral Standard: Electromagnetic compatibility – Requirement and tests
NOTE: Do not use this device in the presence of electromagnetic or other interference outside the normal
range speci ed in EN 60601-1-2.
EN 980: 2008 Symbols for use in labeling of medical devices
EN 1041: 2008 Information supplied by the manufacturer of medical devices
EN 60601-1-11: 2010 Medical electrical equipment – Part 1-11: General requirements for basic safety and
essential performance – Collateral standard: Requirements for medical electrical equipment and medical
electrical systems used in the home healthcare environment
Equipment with type BF applied parts Keep it dry
Operating temperature
Storage temperature
See instruction for use
Internally Powered Equipment
Continuous Operation
IP20: Protected against solid foreign objects of 12.5 mm diameter and greater.
MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC.
For detailed description of EMC requirements please contact Consumer Relations.
Portable and mobile RF communications equipment can a ect MEDICAL ELECTRICAL EQUIPMENT.
Remove the battery from the instrument if it is not required for extended periods of time in order to avoid
damage to the thermometer resulting from a leaking battery.
Please do not dispose of the product in the household waste at the end of its useful life.
To protect the environment, dispose of empty batteries at appropriate collection sites according
to national or local regulations.
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