Ottobock 1C66 Triton smart ankle Instructions D'utilisation page 30

8 Maintenance
► The prosthetic components should be inspected after the first 30 days of use.
► Following an individual period for the patient to get accustomed to the prosthesis, check the
settings of the prosthesis and adapt them to the patient's requirements again as needed.
► Inspect the entire prosthesis for wear during normal consultations.
► Conduct annual safety inspections.
8.1 Applying/removing the footshell
INFORMATION
Pull the Spectra sock over the prosthetic foot to prevent noises in the footshell.
Inserting the foot into the footshell
Recommended tools: 2C100 or 2C101 changing device for footshell
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1) Slide the prosthetic foot into the footshell (see fig. 5).
2) Press the heel of the prosthetic foot into the footshell until it engages.
3) Pull the textile material of the footshell up to the groove in the ankle cover and insert it in the
groove (see fig. 6, see fig. 7).
Removing the footshell
Recommended tools: 2C100 or 2C101 changing device for footshell
>
1) Loosen the textile material of the footshell from the groove in the ankle cover.
2) Push the lock of the footshell to the rear and pull up the heel of the prosthetic foot.
3) Remove the prosthetic foot from the footshell.
9 Disposal
In some jurisdictions it is not permissible to dispose of these products with unsorted
household waste. Disposal that is not in accordance with the regulations of your country
may have a detrimental impact on health and the environment. Please observe the
instructions of your national authority pertaining to return and collection.
10 Legal Information
All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.
10.1 Liability
The manufacturer will only assume liability if the product is used in accordance with the descrip­
tions and instructions provided in this document. The manufacturer will not assume liability for
damage caused by disregard of this document, particularly due to improper use or unauthorised
modification of the product.
10.2 CE Conformity
This product meets the requirements of the European Directive 93/42/EEC for medical devices.
This product has been classified as a class I device according to the classification criteria out­
lined in Annex IX of the directive. The declaration of conformity was therefore created by the man­
ufacturer with sole responsibility according to Annex VII of the directive.
This product meets the requirements of the European Directive 1999/5/EC for radio equipment
and telecommunications terminal equipment. The conformity assessment was drawn up by the
manufacturer in accordance with Annex III of the directive.
The product meets the requirements under the RoHS Directive 2011/65/EU of the European Par­
liament and of the Council of 8 June 2011 on the restriction of the use of certain hazardous sub­
stances in electrical and electronic equipment.
30 | Ottobock