Braun 6021 Thermometer User Manual


 
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Product specifications
Displayed temperature range: 68–108 °F (20–42.2 °C)
Operating ambient temperature range: 50–104 °F (10–40 °C)
Display resolution: 0.1 °F or °C
Accuracy for displayed temperature range: ±0.4 °F (95.9–107.6 °F) (35.5 °C–42 °C)
±0.5 °F (outside this temperature range)
Long term storage ranges
Temperature: –4 °F to 122 °F (–20 °C to 50 °C)
Humidity: 95% non condensing
Shock: withstands drop of 3 feet
Measurement time: 3–7 seconds
Automatic «power down»: 60 seconds
Battery life: 6 months/1000 measurements
Battery type: 2 x MN 1500 or 1.5 V AA (LR6)
Thermometer dimension: 6˝ x 1.7˝ x 1.3˝ (152 mm x 44 mm x 33 mm)
Thermometer weight: 3.6 oz (100 g) without batteries
This infrared thermometer meets requirements established in ASTM Standard E 1965-98 (for the
thermometer system [thermometer with probe cover]). Full responsibility for the conformance of
the product to the standard is assumed by Braun GmbH, 61476 Kronberg, Germany.
ASTM laboratory accuracy requirements for the thermometer only (not including a probe cover)
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).
A clinical summary is available upon request.
This device conforms to the following standards:
DIN EN 60601-1: 3/96 «Medical electrical equipment» –
Part 1: General requirements for safety
DIN EN 12470-5: 2003 «Clinical thermometers» –
Part 5: Performance of infrared ear thermometers (with maximum device)
The Braun ThermoScan thermometer has been proven to be safe. To ensure the best results,
please take the time to read this manual completely and keep it handy for future reference. In the
unlikely event you experience any difficulty using the Braun ThermoScan thermometer, simply
call Welch Allyn toll free at: 1-800-535-6663 (in Canada:1-800-561-8797).
This products conforms to the provisions of the EC directive 93/42/EEC
(Medical Device Directive).
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