24
Contents
1. How to use the CPM device
25
1.1 Fields of application
25
1.2 Therapy objectives
25
1.3 Indications
25
1.4 Contraindications
25
2. Description of the ARTROMOT®-K1 classic
26
2.1 Description of the device components
26
2.2 Description of the control pendant
27
2.3 Explanation of symbols
29
2.4 Explanation of symbols (connections and nameplate)
30
3. Safety information
32
4. Device setup
35
4.1 Connecting the device, performance check
35
4.2 Adjusting the device to the femur length
35
4.3 Adapting the leg support assemblies/footplate
36
4.4 Connecting the potential equalization conductor (SN > 35,000)
37
5. Setting the treatment values
37
5.1 General information on programming ARTROMOT®-K1 classic
37
5.2 Therapy parameter details for the ARTROMOT®-K1 classic
38
6. Care, maintenance, transport
39
6.1 Care/re-use
39
6.2 Maintenance (fuse replacement)
40
6.3. Transport
41
7. Environmental Protection Statement
42
8. Specifications
42
9. Contact
44
10. Technical service
45
10.1 Technical hotline
45
10.2 Shipment
45
10.3 Spare parts
45
11. -Declaration of Conformity
46
Description of the ARTROMOT®-K1 classic
III
ARTROMOT®-K1 classic setup illustrations
VI
12. IEC 60601-1-2:2014 and IEC 60601-1-11:2010
146
12.1 Electromagnetic emissions
146
12.2 Electromagnetic immunity
147
12.3 RF (Radio Frequency) Interference
149
Summary of Contents for 80.00.040
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