PROTEOR ShockWave F20 Notice D'utilisation page 8

category. If necessary, move the bumpers anteriorly (stiffer) or posteriorly (softer) to get the desired stiffness. For permanent
placement, clean off the pre-applied adhesive with acetone and adhere bumpers using cyanoacrylate glue.
Distance from the rear
Foot size (A)
end of the sole (B)
23-25 cm 29 mm / 1.1''
26-28 cm 35 mm / 1.4''
29-30 cm 48 mm / 1.9''
11. TROUBLESHOOTING
CONCERN
• Foot flat occurs too rapidly
• Toe feels excessively stiff
Heel too soft
• Knee hyperextension
• Rapid knee flexion, instability
• Heel to toe progression too fast
Heel too hard
• Lack of energy return sensation
Foot module too
• Flat spot in rollover motion at slow cadences
stiff
• Clicking noise at initial contact
Foot module too
• Excessive toe deflection with high impact
soft
12. WARNINGS
In case of damaged packaging, check the integrity of the device.
Never use the foot without a foot shell and a Spectra sock.
Never loosen the pyramid fastening screws.
The patient must inform their prosthetist if they gain or lose significant weight.
Always use the foot with a sock and shoe. Failure to adhere to this advice may cause product failure, as well as serious
injury.
Make sure that the foot and inside of the foot shell are free of impurities (e.g., sand). The presence of impurities causes
the graphite parts to wear out. Clean the foot according to the instructions (see §16).
After swimming, using in water or if splashed by a liquid, the foot must be cleaned (see §16).
If the patient notices any abnormal behavior or feel any changes in the characteristics of the device (noise, play, excessive
wear...), or if the device has received a severe impact, they should stop using the device and consult their prosthetist.
Failure to follow the instructions for use is dangerous and will void the warranty.
13. CONTRAINDICATIONS
Do not use for a patient whose maximum weight (load carrying included) may exceed 147 kg / 325 lbs.
Do not use for activities associated with a risk of significant impact or excessive overloading.
Do not use for a patient who do noy meet the requirements of a Medicare functional level of K3 or higher.
SYMPTOM
activity
INSTRUCTIONS FOR USE
• Shift socket anteriorly in relation to the foot
• Attach stiffening bumpers. See section 10 above
• Shift socket posteriorly in relation to the foot
• Verify appropriate foot module category
• Consider a lower category foot module
• Consider a higher category foot module
SOLUTION
for installation details
Page 3 of 4
IFU-01-097