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1. How to use the physiotherapy unit
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1.1 Fields of application
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1.2 Therapy objectives
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1.3 Indications
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1.4 Contraindications
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1.5 Secondary effects
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2. Description of the ARTROMOT® ACTIVE-K
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2.1 Description of the device components
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2.2 Description of the control pendant
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2.3 Explanation of symbols
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2.4 Explanation of symbols (connections and rating plate)
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3. Safety information
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4. Device setup
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4.1 Connecting the unit, performance check, Equipment supplied
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4.2 Connecting the external muscle stimulator
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4.3 Adjusting the unit to the femur length
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4.4 Adapting the leg support assemblies/footplate
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5. Setting the treatment values
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5.1 General information on programming ARTROMOT® ACTIVE-K
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5.2 Therapy parameter details
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5.3 Other functions/settings
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6. Operating mode details
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6.1 Passive operating mode (CPM)
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6.2 Active operating mode (CAM)
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6.3 Coordination mode
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7. Care, Maintenance, Transport
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7.1 Care
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7.2 Maintenance (fuse replacement)
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7.3 Transport
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8. Environmental Protection Statement
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9. Specifications
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10. IEC 60601-1-2:2007 and IEC 60601-1-11:2010
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10.1 Electromagnetic emissions
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10.2 Electromagnetic immunity
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10.3 Recommended separation distances
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11. Contact
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12. Technical service
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12.1 Technical hotline
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12.2 Shipment
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12.3 Spare parts
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13. Accessories and Parts for Use with the Device
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14. Declaration of conformity
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Content
Supplied by EME Services Ltd