42
1. How to use the CPM device
43
1.1 Fields of application
43
1.2 Therapy objectives
43
1.3
Indications
43
1.4
Contraindications 43
2. ARTROMOT®-S3 description
44
2.1 Description of the device components
45
2.2 Description of the programming unit
46
2.3 Explanation of symbols
49
2.4 Explanation of symbols (connections and nameplate)
50
3. Safety information
52
4. Device setup
55
4.1 Connecting the device, performance check
55
4.2 Adjusting the device to the patient
56
5. Setting the treatment values
58
5.1 General information on programming ARTROMOT®‑S3 58
5.2 Programming ARTROMOT®‑S3 Standard
60
5.3 Treatment value details – Standard models
60
5.4 Programming ARTROMOT®‑S3 Comfort
64
5.5 Protocol details – Comfort model
65
5.6 Examples of use/sample protocols
69
6. Care, Maintenance, Transport, Conversion
71
6.1 Care/re‑use
71
6.2 Maintenance (fuse replacement)
71
6.3 Transport
73
6.4 Conversion
74
7. Environmental Protection Statement
75
8. Specifications
75
9. Contact
77
10. Technical Service
78
10.1 Technical hotline
78
10.2 Shipment
78
10.3 Spare parts
78
11. -Declaration of Conformity
79
Contents
Device description ARTROMOT®-S3
ΙΙΙ
Figures ARTROMOT®-S3
VΙΙΙ
Symbol overview ARTROMOT®-S3
V
12. IEC 60601-1-2 and IEC 60601-1-11
248
12.1 Electromagnetic emissions
248
12.2 Electromagnetic immunity
249
12.3 Recommended separation distances
251
Summary of Contents for ARTROMOT-S3
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