Bebe Confort No touch thermometer User Manual
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9 - REPLACING BATTERIES
A / Monitoring battery voltage
• • When the batteries are low, the battery symbol appears at
the bottom of the screen. You should therefore keep a set of new
AAA - 1.5 v batteries to replace the old ones as soon as possible
(Figure 5).
However the thermometer can continue to work normally until both
Lo and
symbols are displayed at the same time (Figure 6)
B / Taking out and replacing the batteries
• Take the old batteries out of their housing and put in two new AAA batteries, preferably alkaline ones,
just as when first operating the thermometer (Chapter 2), observing the polarities indicated.
• Keep dead batteries out of the reach of children and observe the regulations in force for disposing
of them.
10 - TECHNICAL FEATURES
1 Type
Infrared no touch thermometer
2 Measurement ranges
Body temperatures 10°C to 50°C
Household temperatures 0°C to 100°C
3 Accuracy
Body temperatures ± 0.3°C between 22°C and 40°C
Household temperatures 20°C ± 1°C / > 20°C ± 5%
4 Measurement scale
Degrees Celsius
5 Resolution
0,1°C
6 Optimal measurement distance
4 to 8cm
7 Memory
10
8 Switch off
Automatic after 30 seconds
9 Power
Two AAA – 1.5 v alkaline batteries
10 Operating conditions
Ambient temperature 16°C to 35°C with maximum
relative humidity of 95% (without condensation)
11 Storage conditions
- 25°C to + 55°C with maximum humidity of 95%
(without condensation)
12 Control signals
«Lo» and «Hi»: temperatures outside ranges
low battery
13 Dimensions
141mm x 42mm x 55.5mm
14 Weight
120 grams with batteries
11 - WARRANTY
This product is guaranteed for two years from the date of purchase. Damage caused by incorrect handling
is not covered by the warranty. The batteries and packaging are also excluded from the warranty. All other
damage is excluded. Always attach the proof of purchase to any claim and send to Dorel at one of the
addresses listed in these instructions.
Reference to ASTM (E1965-98), EN 980: 2003, IEC/EN 60601-1-2, ISO 14971 standard.
This device meets the requirements of Directive 93/42/CEE concerning medical devices.
Figure 6
Figure 5
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