Braun ThermoScan RT 3020 Manual Del Usuario página 7

Calibration
The thermometer is initially calibrated at the time of manufacture .
If this thermometer is used according to the use instructions, periodic
readjustment is not required . If at any time you question the accuracy of
temperature measurements, please contact an authorized Kaz Service
Center .
Manufacturing date is given by the LOT number located in the battery
compartment . The first three (3) digits represent the Julian date that the
product was manufactured and next two (2) digits represent the last
two numbers of the calendar year the product was manufactured . The
last identifier are the letters that represent the manufacture .
An example: LOT 15603RAD
this product has been manufactured June 5, 2003 at RAD .
NOTE: the letter(s) at the end of the LOT number represent the
manufacturer name .
Product specifications
Model:
Displayed temperature range:
Operating ambient
temperature range:
Display resolution:
Accuracy for displayed
temperature range:
Clinical repeatability:
Humidity:
Battery life:
If device is not used within specified temperature and humidity ranges
the technical accuracy cannot be ensured .
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IRT 3020
34 °C – 42 .2 °C
(93 .2 °F – 108 °F)
10 °C – 40 °C
(50 °F – 104 °F)
0 .1 °C or °F
± 0 .2 °C (35 .5 – 42 °C)
(95 .9 – 107 .6 °F)
± 0 .3 °C (outside this
temperature range)
± 0 .25 °C (± 0 .45 °F)
≤ 95% non-condensing
2 years /
1000 measurements
Type BF equipment
Subject to change without notice .
Standard Reference Edition Title
EN 12470-5 2003 Clinical Thermometers – Part 5:
Performance of Infrared Ear
Thermometers (with maximum device) .
EN 60601-1 2006 Medical electrical equipment – Part 1:
General requirements for basic safety
and essential performance .
EN ISO 14971 2007 Medical devices – Application of risk
management to medical devices .
EN ISO 10993-1 2009 Biological evaluation of medical devices
– Part 1: Evaluation and Testing .
EN 60601-1-2 2007 Medical electrical equipment – Part1-2:
General requirements for basic safety
and essential performance
– Collateral standard:
Electromagnetic compatibility –
Requirements and tests .
This product conforms to the provisions of the EC directive
93/42/EEC (Medical Device Directive) .
MEDICAL ELECTRICAL EQUIPMENT needs special precautions
regarding EMC . For detailed description of EMC requirements please
contact an authorized local Service Centre .
(See Guarantee Card) .
Portable and mobile RF communications equipment can affect
MEDICAL ELECTRICAL EQUIPMENT .
Please do not dispose of the product in the household
waste at the end of its useful life . Disposal can take place at
your local retailer or at appropriate collection points provided
in your country .
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