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Baylis RFP-100A - ALERT CODES

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© 2012-2019 Baylis Medical Company Inc. 36 of 48 DMR RFP-100A 3.3 V-13 29-May-2020_EN.docx
9.4. ALERT CODES
Summary of Alert Codes, Displayed Text, and Description
Alert Code
Displayed Text
Description
A005
High Impedance Detected.
Check device and all cable
connections
Greater than 6000 ohm measured during
RF energy delivery. May indicate poor
connection between Device and connector
cable or poor patient contact with
dispersive electrode.
A006
Low Impedance Detected
Less than 100 ohm measured during RF
energy delivery. Device may be in contact
with a metal object.
A007
Check ground pad contact
with patient. Replace
grounding pad if necessary.
Impedance between the conductors of a
dual foil dispersive electrode is greater
than 150 ohm. This may indicate poor
patient contact.
A008
Check ground pad contact
with patient. Replace
grounding pad if necessary.
Impedance between the conductors of a
dual foil dispersive electrode is greater
than 150 ohm. This may indicate poor
patient contact.
A009
Check ground pad contact
with patient. Replace
grounding pad if necessary.
Impedance between the conductors of a
dual foil dispersive electrode is greater
than 150 ohm. This may indicate poor
patient contact.
A010
Check all ground pad
connections and ground pad
contact with patient.
Open circuit between conductors of
dispersive electrode connection. May
indicate faulty dispersive electrode or
poorly connected dispersive electrode.
A011
Device ID has changed.
Error with connector cable may have
altered Device specific settings. The
connector cable should be checked for any
problems.
A012
Invalid device detected.
Record alert code and contact
Baylis Clinical Support.
Invalid or broken connector cable
connected to the Generator.
A013
Unsupported device detected.
Record alert code and contact
Baylis Clinical Support.
Device does not have supported output
parameters.
A014
Device connection lost.
Connector cable was disconnected or
failed during RF energy delivery.
A017
The connected device
conflicts with the current
channel configuration.
Device parameters have been corrupted.
Contact Baylis Clinical Support.
A018
Device not connected
Either connector cable is not functioning
or not connected when attempting to

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