DJO Global ARTROMOT-K1 Modo De Empleo página 40

Contents
Device description ARTROMOT®-K1
Symbol overview ARTROMOT®-K1
Figures ARTROMOT®-K1
1. How to use the CPM device
1.1 Fields of application
1.2 Therapy objectives
1.3 Indications
1.4 Contraindications
2. ARTROMOT®-K1 description
2.1 Description of the device components
2.2 Description of the programming unit
2.3 Explanation of symbols
2.4 Explanation of symbols (connections and nameplate)
3. Safety information
4. Adjusting the device
4.1 Connecting the device, performance check
4.2 Connecting the external muscle stimulator ¹
4.3 Adjusting the device to the femur length
4.4 Adapting the leg support assemblies/footplate
5. Setting the treatment values
5.1 General information on programming ARTROMOT®-K1
5.2 Programming ARTROMOT®-K1 standard models
5.3 Treatment value details - standard models
5.4 Programming ARTROMOT®-K1 Comfort models
5.5 Protocol details - Comfort models
6. Care, Maintenance
6.1 Care
6.2 Maintenance (fuse replacement)
6.3. Transport
7. Environmental protection statement
8. Specifications
9. IEC 60601-1-2:2007 and IEC 60601-1-11:2010
9.1 Electromagnetic emissions
9.2 Electromagnetic immunity
9.3 Recommended separation distances
10. How to reach us
11. Technical Service
11.1 Technical Hotline
11.2 Shipment
11.3 Spare parts
12. Declaration of conformity
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