VISUSCOUT 100-GA-GB-031219
5
Symbol
Description
0598
The CE mark with notified body identification
number on this product indicates it has been
tested and conforms to the provisions noted
within the 93/42/EEC Medical Device Directive.
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 the VISUSCOUT 100
that in normal use necessarily comes into
physical contact with the patient.
9V, 1.1 A
Charger polarity symbol, voltage and power
Interference may occur in the vicinity of
equipment.
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.
Caution: Federal law restricts this device to sale
by or on the order of a physician or licensed
practitioner.
Summary of Contents for VISUSCOUT 100
Page 1: ...VISUSCOUT 100 Mobile Retinal Camera User Manual...
Page 2: ...VISUSCOUT 100 GA GB 031219...
Page 57: ...VISUSCOUT 100 GA GB 031219 55...
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