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INSTRUCTIONS FOR USE
Symbol used
Document Number: 80028190
Version: E
Description
Indicates the need for the user to consult the
instructions for use for important cautionary
information such as warnings and precautions.
Indicates the device do not contain natural
rubber or dry natural rubber latex
Indicates the authorized representative in the
European Community
Indicates the Medical Device complies to
REGULATION (EU) 2017/745
Indicates a Warning
Indicates the need for the user to consult the
instruction for use
Medical Electrical Equipment Evaluated
Type B applied part
Degree of protection against the ingress of
water
Equipotential
Failure to Follow the Operating Instructions
Could Put the Patient or Operator at Risk.
Page 11
English
Reference
EN ISO 15223-1
EN ISO 15223-1
EN ISO 15223-1
MDR 2017/745
IEC 60601-1
EN ISO 15223-1
UL60601-1,
EN 60601-1,
IEC 60601-1,
IEC 60601-2-46,
IEC 60601-1-2
N/A
N/A
N/A
IEC 60601-1
Issue Date: 16 MAY 2022
Ref Blank Template: 80025117 Ver. F
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