PROTEOR MATIK Notice D'utilisation page 8

3. INTENDED USERS/INDICATIONS
This medical device is supplied to healthcare professionals (prosthetists/orthotists) who then instruct the patient in how to use it. The
prescription is drawn up by a doctor. The doctor works with a prosthetist/orthotist to assess whether the patient is suited to using the device.
This device should be used on ONE PATIENT ONLY. It must not be reused on other patients.
The maximum knee flexion is 170°. This flexion may, however, be limited by the volume of the socket or by the cosmetic covering.
4. CLINICAL BENEFITS
The device allows:
•
Everyday mobility with minimum maintenance
•
The patient to choose a lighter and smaller knee.
•
Flexion of up to 170° for sitting or kneeling.
•
Good clearance between the foot and the ground in the swing phase, to avoid contact.
•
High levels of stability and safety in the stance phase thanks to the 4-axis joint geometry.
5. ACCESSORIES AND COMPATIBILITIES
Ref.
Proximal adapter
Distal adapter
6. ASSEMBLY AND FITTING TO THE PATIENT
A. Aligning
Static alignment:
In the sagittal plane, the load line passes through the greater trochanter and between 0 and 10 mm in front of the axis of the
knee.
Align the foot in compliance with the manufacturer's instructions.
In the frontal plane, the load line passes through the middle of the socket, through the middle of the knee and between the
first and second toes.
This device is exclusively intended to be used as prosthetic equipment for patients who have undergone
transfemoral amputation, hip disarticulation or knee disarticulation. It is specifically recommended for
active or slightly active patients (L2/L3) and allows them to perform everyday activities.
Maximum weight (including carried load): 125 kg
Not suitable for children.
1K179+ 1K183
Anchor 1K173 or 1K176
1K177 (max. weight 100 kg)
Connectors 1K172 or 1K207-HD
Tube and
connector
INSTRUCTIONS FOR USE
1P200
1D41-HD and 1G01-HD
1D52-P6
1P200-KD
1K179
1K184
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