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English
Type: BFH175US Infrared Forehead Thermometer
Measuring range: 93.2°-109.4°F (34°-43°C)
Resolution: 0.1 °F or °C
Accuracy (Laboratory): 0.4 °F for 95 °F – 107.6 °F
(0.2 °C for the range 35 °C – 42 °C)
outside that range ±0.5°F/0.3°C
(Ambient Temperature: 59 °F to 104 °F
(15 °C to 40 °C)
This thermometer displays a
calculated oral equivalent estimate.
Display: Liquid Crystal Display, 4 digits plus special icons
Acoustic: Audio:
Normal temp range=1 long beep for 0.4 second
duration
Fever=10 short beeps for 0.2 second duration
Operating temperature: 59°F- 104°F (15°C- 40°C)
Automatic Switch-off: Approx. 30 seconds after last measurement has
been taken
Weight: 3.32 oz. (with batteries), 2.52 (without batteries)
Long term storage ranges
Storage/transport temperature: –13 °F to 131 °F (–25 °C to 55 °C)
Humidity: 15–95% non condensing
Battery: (2) AAA Batteries - at least 500 measurements
Pressure: 70kPa-106kPa(0.7atm-1.06atm)
This thermometer is an adjusted mode thermometer that provides an oral equivalent reading.
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 USA, Inc., a
Helen of Troy Company, Health & Home, 400 Donald Lynch Blvd., Suite 300, Marlborough, MA 01752
ASTM laboratory accuracy requirements, for the thermometer only in the display range of 96.8 °F to 102.2 °F
(36 °C to 39°C) for infrared thermometers is ±0.5 °F (±0.3 °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 device conforms to the following standards:
EN 60601-1:2014 Medical electrical equipment. General requirements for basic safety and essential
performance
ISO 80601-2-56:2017 Particular requirements for basic safety and essential performance of clinical
thermometers for body temperature measurement
ASTM E1965-98:2016 - Standard Specification for Infrared Thermometers for Intermittent
Determination of Patient Temperature
IEC 60601-1-2:2014: 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 specified in IEC 60601-1-2.
ISO 15223-1:2016: Symbols for use in labeling of medical devices
EN 1041: 2008 Information supplied by the manufacturer of medical devices
IEC 60601-1-11:2015 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
Product specifications
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