DJO 80.00.035, Руководство по эксплуатации

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38
1. How to use the CPM device 39
1.1 Fields of application 39
1.2 Therapy objectives 39
1.3 Indications 39
1.4 Contraindications 39
2. Description of the ARTROMOT®-SP3 40
2.1 Description of the device components 41
2.2 Description of the control pendant 42
2.3 Explanation of symbols 45
2.4 Explanation of symbols (connections and nameplate) 46
3. Safety information 48
4. Device setup 52
4.1 Connecting the device, performance check 52
4.2 Adjusting the device to the patient 53
5. Setting the treatment values 54
5.1 General information on programming the ARTROMOT®-SP3 54
5.2 Programming the ARTROMOT®-SP3 Standard models 55
5.3 Treatment value details – Standard models 56
5.4 Programming the ARTROMOT®-SP3 Comfort models 59
5.5 Protocol details – Comfort model 60
6. Care, Maintenance, Transport, Conversion 64
6.1 Care / re-use 64
6.2 Maintenance (fuse replacement) 65
6.3 Transport 67
6.4 Conversion 68
7. Environmental protection statement 69
8. Specifications 69
9. Contact 71
10. Technical service 72
10.1 Technical hotline 72
10.2 Shipment 72
10.3 Spare parts 72
11. -Declaration of Conformity 73
Contents
Description of the ARTROMOT®-SP3 ΙΙΙ
ARTROMOT®-SP3 setup illustrations VΙΙΙ
Symbol overview ARTROMOT®-SP3 V
12. IEC 60601-1-2 and IEC 60601-1-11 226
12.1 Electromagnetic emissions 226
12.2 Electromagnetic immunity 227
12.3 RF (Radio Frequency) Interference 229