Safety Precautions - Blancone ARCUS+ Instrucciones De Uso

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III. SAFETY PRECAUTIONS
GENERAL WARNINGS:
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BLANCONE ARCUS
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ments of the Medical Devices Regulation - MDR (EU) 2017/745. In order to be used safely for staff
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and patients, the following rules must be observed:
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Unique Device Identifier
Indicates a carrier that contains Unique Device Identifier information.
Catalogue number
Indicates the manufacturer's catalogue number so that the medical device can be identified.
Serial number
Indicates the manufacturer's serial number so that a specific medical device can be iden-
tified.
Batch code
Indicates the manufacturer's batch code so that the batch or lot can be identified.
Applied part type B according to electric safety classification.
Temperature limit
Indicates the temperature limits to which the medical device can be safely exposed.
Humidity limitation
Indicates the range of humidity to which the medical device can be safely exposed.
Waste Electrical and Electronic Equipment (WEEE)
According to Directive 2012/19/EU, this symbol indicates that the product
should not be disposed of as urban waste at the end of its operating life.
Fragile
Indicates a medical device that can be broken or damaged if not handled carefully.
European Conformity
Indicates conformity with local laws and regulations within the European Economic Area.
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is a Class I accessory to a medical device and it meets the strict require-
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