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miniland thermokit Bedienungsanleitung Seite 15

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6. Do not bend or bite or pull the unit.
7. Do not attempt to disassemble the unit except to replace the battery.
8. The measurement reading maybe incorrect when the body temperature is lower than ambient
temperature.
9. Suitable for measuring children's body temperatures.
10. It is designed and manufactured complying with relevant requirements in ISO80601-2-56: Per-
formance of Compact electrical thermometers (non-predictive and predictive) with maximum device.
11. It has passed EMC emission test, immunity test according to EN60601-1-2 and biocompatibili-
ty test according to MDD annex 1.
12. According to the degree of protection against electric shock, it is classified to BF, in accordance
with EN60601-1.
13. This product meets the basic safety and essential performance requirements indicated in the
IP22 conditioning test (IP22: Protection level against solid foreign objects and dripping water)
14. Never allow chemical solutions to come into contact with the thermometer and keep away from
direct sunlight or heat sources as well as strong electromagnetic sources to avoid interference.
15. Dispose of the product and battery according to relevant national regulations.
16. Please take out the battery if the unit is going to be used for a long time.
17. This thermometer is designed and manufactured in compliance with the relevant requirements
in EN12470-3: Compact electrical thermometers (comparison and extrapolation) with maximum
device.
18. This thermometer should be used in an environment with a temperature between 10ºC to 35ºC
and a humidity of 40% to 80%. During storage, the temperature should be between -10ºC to 40ºC
and the humidity between 30% to 90%.
19. Please replace the battery before claiming replacement with a new product.
Battery Warning: Use only the batteries indicated.
Caution! Be sure that both the battery and the thermometer are kept away from children.
3.6. NORMALIZED SYMBOLS
Attention: Read the operating Instructions for use!
Applied part of type BF
Disposal in accordance with Directive 2012/19/EU (WEEE)
Complies with the European Medical Device Directive (93/42/EEC) and
amended by directive 2007/47/EC requirements.
2460
Notified body 2460: DNV GL Nemko Presafe AS
Batch code
The name and the address of the manufacturer.
Authorized Representative in the European Community
15
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89511-289511-189511-3

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