The dynamic alignment is performed in accordance with good professional practices.
B. Finishing
Comply with traditional good professional practices in terms of fitting the malleolar clip to cosmetic elements.
7. DETECTING ANY MALFUNCTIONING
If you notice that the device is behaving abnormally or if its characteristics feel different, or if it has been badly knocked, consult your
prosthetist/orthotist.
8. WARNINGS, CONTRAINDICATIONS, SIDE EFFECTS
A. Warnings
Using the foot in a way that goes against the advice given by your prosthetist/orthotist may damage or degrade the foot's components
(e.g. carrying heavy loads, excessive stresses, use after its service life has expired, etc.)
The device is only resistant to fresh water and to bad weather conditions, and requires compliance with the care instructions
specified in §9.A.
B. Contraindications
This foot is not intended to be used for activities associated with a risk of significant impact or excessive loading.
This foot is not resistant to salt water or chlorinated water.
C. Side effects
There are no side effects directly associated with the device.
Any serious incident that occurs which relates to the device must be reported to the manufacturer and to the competent authority
of the member state in which the incident occurred.
9. MAINTENANCE, STORAGE, DISPOSAL AND SERVICE LIFE
A. Maintenance/cleaning
Clean the foot shell with a damp cloth or sponge.
All work on the foot should be performed by the prosthetist/orthotist; no other operations, such as lubrication, work on the fastenings
or other work, need to be performed.
After being used in fresh water or in bad weather conditions
•
Rinse the foot with clean water
•
Dry thoroughly
The malleolar clip may need to be replaced (in the event of wear, loss, etc.)
B. Storage
Service and storage temperature: -20°C to +60°C
Relative humidity of the air: no restrictions
C. Disposal
The various components of the foot are considered as special waste: stainless steel, thermoplastic (polyamide, polyethylene),
polyurethane. They must be treated in accordance with current, applicable legislation.
INSTRUCTIONS FOR USE
Centre of
coxofemoral
joint
Centre of
knee joint
Knee fully
extended
Load
line
5 - 15 mm
Vertical axis
passing through the
centre of the socket
at the knee and the
pyramid
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