GS corpuls3 - F Safety Information

User Manual corpuls
3
Appendix
ENG - Version 2.1 – P/N 04130.2 303
Precision of the Energy Released for Shock Spoons
Selected
energy
(in Joule)
Nominal energy released in comparison to patient
impedance
Accuracy:
Load impedance (in Ohm)
10
15
20
25
50
100
150
2
1.5
1.5
1.7
1.7
2.2
2.1
2.0
± 3J
5
4.0
4.2
4.5
4.9
5.6
5.5
5.2
± 3J
10
8.8
9.2
9.0
9.2
11.2
11
10.2
± 15 %
20
18.1
19.4
20.2
20.8
22.8
23.7
22.6
± 15 %
30
26.4
28.6
29.5
31.3
34.5
33.4
32.7
± 15 %
40
36.8
37.7
39.8
40.8
45.9
45.8
43.3
± 15 %
50
46.3
49.6
49.2
51.2
57.7
56.1
54.7
± 15 %
Table A-32 Precision of the energy released for shock spoons
F Safety Information
Warning
Failure to observe this safety information may result in injuries to the patient and
users.
General
• The corpuls
3
is not intended for operation in the vicinity of readily inflammable anaesthetics or
other flammable substances, particularly in an oxygen-rich environment.
• The corpuls
3
must not be stored or operated near a switched-on magnetic resonance imaging
(MRI) unit.
• The corpuls
3
must not be operated near ionising (radioactive) radiation intended for therapeutic
purposes.
• The corpuls
3
is not intended for operation in connection with a high frequency surgical device.
• To avoid stumbling or the patient, user or third parties being entangled in or strangled by cables,
they should be led around the patient, as all medical implements.
• When connecting intermediate cables and sensors, make sure there are no foreign objects
between the plug connections.
Alarm function
• Do not leave the patient unattended in the following cases:
- if the alarm function is deactivated or
- device is in defibrillation mode.
• In case of unsupervised monitoring of vital parameters, it is recommended that you monitor a
further vital parameter with another independent monitoring system.
• The option for monitoring measured values may be disabled when switching on the corpuls
3
(see chapter 7 Configuration, p. 137). Therefore make sure that the alarms are correctly
configured.
• Heart rate is only monitored when all electrodes of the ECG monitoring cable or the corPatch
electrodes are connected to the patient (see chapter 7 Configuration, p. 137).
• Check the settings of the alarm limits before each monitoring phase.
• Set the volume of the acoustic alarm so that it cannot be overheard in loud environments.