USER MANUAL 16-2040N / 16-2041N / 16-2042N
Rev. 07/2016
2.3 MEDICAL DEVICE VIGILANCE
Like any medical device, this unit is subject to the provisions related to medical device vigilance; therefore
any serious malfunction must be promptly reported to the proper authority and to us, giving as much detailed
information as possible. Please refer to the second page for our contact details.
2.4 END OF LIFE
This device carries the recycling symbol in accordance with European directive 2002/96/CE on Waste
Electrical and Electronic Equipment (DEEE or WEEE).
By following the correct procedures for disposing of this device you will be contributing to the prevention of
any consequences that could be harmful to the environment or human health.
The symbol to be found on the device and/or in the accompanying documentation indicates that this
product may on no account be treated as household waste. It must therefore be delivered to a waste
collection point for the recycling of electrical and electronic equipment. For disposing of the device, please
observe the standards applied in the country of installation. To obtain complete details about the treatment,
recovery and recycling of this appliance, please contact your closest dealer to know how to proceed.
3. DESCRIPTION OF THE FRONT AND BACK PANEL
FRONT
Description
BACK
Description
A
5.7-inch LCD screen
1
CO
2
Input
B
Warning light
2
On/Off switch
C
Tubing connector for patient
insufflation
3
Fuse housing
D
Tubing connector for external
desufflation
4
Mains socket
E
Low/high flow selector button
5
Equipotential socket
F
Start/stop insufflation
6
Labeling
G
Selection and validation thumbwheel
H
Start/standby button
I
Start/standby LED
FRONT PANEL
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