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INSTRUCTIONS FOR USE
Symbol used
Document Number: 80028198
Version: F
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
NOTE: Components of the Lateral-to-Prone
configuration manufactured prior to August
2017 may not be CE marked. Check individual
product for details. See page 23.
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
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
Issue Date: 03 FEB 2023
Ref Blank Template: 80025117 Ver. F
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