European certificate of conformity
CE marking with notified body identification numbering indicates
the conformity of 93/42/EEC Medical Device Directive for class IIa
devices and CE marking without notified body identification
numbering indicates the conformity of 93/42/EEC Medical Device
Directive for class I devices.
Read accompanying user documentation indicates that important
operating instructions are included in this User’s and Maintenance
Manual. Failure to follow these instructions could place the patient
or operator at risk.
Type BF applied parts.
Applied part is a part of Smartscope that in normal use necessarily
comes into physical contact with the patient.
Charger polarity symbol, voltage and power
Interference may occur in the vicinity of equipment (in case device
has WLAN functionality).
Prepare the device for reuse or separate collection as specified by
Directive 2002/96/EC of the European Parliament and Council of the
European Union on Waste Electronic and Electrical Equipment
(WEEE). If this product is contaminated, this directive does not
apply.
WARNING
Indicates a hazardous situation which could result in patient injury,
harm or death if the appropriate safety precautions are not
followed.
CAUTION
Indicates a situation which could result in device harm, damage or
mal-function if the appropriate cautions / precautions are not
followed.
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