Fault, Cause, Remedy - Dräger AGS Gebrauchsanweisung

English/English US
WARNING
Risk of personal injury
When using the AGSS without ejector, a re-
ceiving system complying with the EN ISO
9170-2 standard must be used.
WARNING
Risk of personal injury
Make sure to install the hoses without loops
and kinks.
CAUTION
Risk of patient injury
Check the flow tube for cracking before every use.
Replace flow tube if damaged.
D
A
B
 The upper edge of the float (A) in the flow tube
(B) muss stay within the two marks (C).
WARNING
Risk of patient injury
Do not cover the side openings (D) of the re-
ceiving system. Otherwise there may be a
shortage of fresh gas in the breathing system.
Shut-down
A
1 Disconnect the connector of the scavenging
hose (A) on the terminal unit of the disposal sys-
tem (B).
10

Fault, Cause, Remedy

Fault Cause
Upper edge of Particle filter
the float is be- blocked.
low the lower
mark
Insufficient suc-
tion power of
the ejector in
the AGSS ter-
minal unit.
C
Upper edge of No particle fil-
the float is float- ter.
ing above the
upper mark.
Suction power
of the ejector in
the AGSS ter-
minal unit is too
B
high.
Float is stuck in Faulty flow
the flow tube, tube.
position does
not change
during startup
Reprocessing
Safety information
WARNING
Risk due to inappropriately reprocessed prod-
ucts
Reusable products must be reprocessed, oth-
erwise there is an increased risk of infection.
– Follow the infection prevention policies and
reprocessing regulations of the health-care
facility.
– Follow the national infection prevention
policies and reprocessing regulations.
– Use validated procedures for reprocessing.
– Reprocess reusable products after every
use.
– Follow the manufacturer's instructions for
cleaning agents, disinfectants, and repro-
cessing devices.
CAUTION
Risk due to faulty products
Signs of wear, e.g., cracks, deformation, discolor-
ation, or peeling, may occur with reprocessed
products.
Check the products for signs of wear and replace
them if necessary.
Information on reprocessing
Follow the national infection prevention policies and
Remedy
reprocessing regulations.
Replace parti-
Follow the infection prevention policies and repro-
cle filter,
cessing regulations of the health-care facility (e.g.,
page 12.
concerning the reprocessing cycles).
Ask DrägerSer-
Classifications for reprocessing
vice or special-
ized service
Classification of medical devices
personnel to set
the suction
The classification depends on the intended use of
power to the
the medical device. The risk of infection transmis-
working range
sion through the application of the product to the pa-
of the anesthet-
tient without proper reprocessing is the basis of the
ic gas receiving
Spaulding classification.
system AGS.
Classification Explanation
Ask DrägerSer-
vice or special- Non-critical
ized service
personnel to re-
Semi-critical
place the ejec-
tor in the AGSS
terminal unit.
Ask DrägerSer-
Critical
vice or special-
ized service
personnel to
check the di-
Categorization and classification
posal line in re-
The following classification is a recommendation
gard to ram
from Dräger.
pressure
(length, diame-
Category
ter, pressure
conditions in
Flow tube
the climate ex-
Container for buf-
haust air chan-
fer volume
nel).
Transfer hoses
Fit particle filter,
and scavenging
page 12.
hoses
Ask DrägerSer-
vice or special-
ized service
personnel to set
the suction
Plugs
power to the
working range
of the anesthet-
Adapters
ic gas receiving
system AGS.
Replace flow
AGS header
tube, page 12.
Before reprocessing
The patient-specific accessories and consumables
must be removed from the device and, if necessary,
disassembled.
 Reprocess the reusable products in accordance
with the instructions given in these instructions
for use.
 Dispose of the disposable products.
Removing the accessories
 Disconnect the transfer hose, possible second
transfer hose, scavenging hose and optional
sample gas return line from receiving system
and basic device.
 Disconnect receiving system from basic device.
 Rotate buffer volume container to the left and re-
move.
 Remove flow tube and filter if the AGS header is
to be reprocessed in a washer-disinfector.
Instructions for use Anesthetic gas receiving system AGS
Components that come into con-
tact only with skin that is intact
Components that carry breathing
gas or come into contact with
mucous membranes or patho-
logically altered skin
Components that penetrate skin
or mucous membranes or come
into contact with blood
Classifica- Part number
tion
Non-critical M33293
Semi-critical M33292
Semi-critical M35016
M33955
M33295
M33296
M35015
M33297
M33298
M33299
M36746
Semi-critical G60440
G60495
G60580
Semi-critical M36048
8413433
M29430
Semi-critical MX08627