Dräger Fabius plus User Manual

For your safety and that of your patients
12 Instructions for use Fabius plus SW 3.n
Product-specific safety information
WARNING
Risk of misinterpretation
Misinterpretation of measured values or other
parameters or misdiagnosis can endanger
the patient.
Do not make therapeutic decisions based
solely on individual measured values and
monitoring parameters. Therapeutic
decisions must be made solely by the user.
WARNING
Risk of burns
Conductive breathing hoses or face masks
can cause burns during HF surgery.
Do not use this type of hose and mask
combined with HF surgery.
WARNING
Risk of malfunction
Device failure or user error can compromise
the correct functioning of the device. The
medical device does not react automatically
to certain changes in the patient condition,
operating errors, or failure of components.
Continuously monitor the medical device so
that corrective measures can be initiated
immediately.
WARNING
Risk of device failure
The device can fail if the power supply is
interrupted.
Always connect the device on an
uninterruptible power supply.
WARNING
Risk of patient injury
Every user has the obligation to assess
independently which components are
required corresponding to the specific
prerequisites for the anesthesia workstation.
In accordance with the general safety
standards for anesthesia systems, additional
monitoring of the concentrations of CO
2 and
anesthetic agent is required when operating
the device. To guarantee patient safety,
however, the following components must
always be used:
–O
2 monitor
– Pressure monitor
– Volume monitor
WARNING
Risk of malfunction
Unallowed modifications to the medical
device lead to malfunctions.
This medical device may not be changed
without permission from Dräger.
WARNING
Risk of accidental movement of the medical
device
During operation the medical device can
move accidentally.
Activate the castor brakes.

Dräger Fabius plus Specifications

General

Brand	Dräger
Model	Fabius plus
Category	Medical Equipment
Language	English