DJO Global ARTROMOT-E2 COMPACT, Operating Instructions Manual

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1.1 Fields of application
The ARTROMOT®-E2/-E2 compact is a
motor-operated C ontinuous P assive M o-
tion ( CPM ) device providing motion to the
elbow joint.
suitable for use in hospitals, clinics,
general practices and rental services, it is
an important supplement to medical and
therapeutic treatment.
1.2 Therapy objectives
CPM therapy with the ARTROMOT®-E2/-E2
compact is mainly used to prevent the
negative efects of immobilization, to allow
patients to regain painless mobility of joints
at an early stage and to promote healing and
achieve a positive functional result.
Other objectives of therapy include:
− improvement of joint metabolism
− prevention of joint stifness (arthroibrosis)
− promotion of the regeneration and healing
of cartilage and damaged ligaments
− faster hematoma/luid resorption
− improved lymph and blood circulation
− thrombosis and embolism prophylaxis
1.3 Indications
The CPM device is indicated in the treat-
ment of most injuries and postoperative
conditions and diseases of the elbow joint.
Examples:
− joint distortion and contusion
− arthrotomy and arthroscopy procedures
in combination with synovectomy,
arthrolysis or other intra-articular
interventions
− all types of arthoplasty
− mobilization of joints in anesthetized
patients
− exercise-stable fractures after surgery
and pseudoarthrosis
− endoprosthetic implants
− myoplasty
− corrective osteotomy
1.4 Contraindications
Do NOT use the ARTROMOT®-E2/-E2
compact on patients with:
− acute inlammatory processes in the
joints, unless on the order of a physician
− spastic paralysis
− unstable osteosynthesis
1. How to use the CPM device
Device description ARTROMOT®-E2 II
Figures ARTROMOT®-E2 IV
Symbol overview ARTROMOT®-E2/-E2 compact V
Figures ARTROMOT®-E2 compact VII
Device description ARTROMOT®-E2 compact VIII
1. How to use the CPM device 49
1.1 Fields of application 49
1.2 Therapy objectives 49
1.3 indications 49
1.4 Contraindications 49
2. Description of the ARTROMOT®-E2/-E2 compact 50
2.1 description of the ARTROMOT®-E2 device components 50
2.2 description of the ARTROMOT®-E2 compact device components 51
2.3 description of the programming unit 52
2.4 Explanation of symbols 55
2.5 Explanation of symbols (connections and nameplate) 56
3. Safety information 58
4. Device setup 62
Note: See device description on pages II / III and VIII / IX
4.1 Connecting the ARTROMOT®-E2/-E2 compact, performance check 62
4.2 Adjusting the device to the patient 63
5. Setting the treatment values 66
5.1 General information on programming the ARTROMOT®-E2/-E2 compact 66
5.2 Programming the ARTROMOT®-E2/-E2 compact 68
5.3 Therapy parameter details 69
5.4 Application and programming examples 77
6. Care, Maintenance, Transport, Conversion 79
6.1 Care 79
6.2 Maintenance (fuse replacement) 79
6.3 Transport 81
6.4 Conversion 84
7. Environmental Protection Statement 86
8. Specifications 86
9. IEC 60601-1-2:2007 and IEC 60601-1-11:2010 88
9.1 Electromagnetic emissions 88
9.2 Electromagnetic immunity 89
9.3 Recommended separation distances 91
10. Contact 92
11. Technical service 93
11.1 Technical hotline 93
11.2 shipment 93
11.3 spare parts 93
12. Declaration of conformity 94
Contents