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ORTOTEK A.Ş.
Ziya Gökalp Cad. 68/21
Kolej/Ankara/TÜRKEI
Distributed by:
Uniprox GmbH & Co.KG, H.-Heine-Str.4, 07937 Zeulenroda-Triebes
Ein Unternehmen der Bauerfeind Gruppe – www.uniprox.de
Qualität und Funktion
Gebrauchsanweisung
Instruction Manual
Karbon-Füße
F120 Chopart
F125 Chopart Plus
F130 Symes-Tech Plus
F140 Pars X3
F150 Synergy® X3 LP
F160 Synergy® X3
Carbon-Feet
F120 Chopart
F125 Chopart Plus
F130 Symes-Tech Plus
F140 Pars X3
F150 Synergy® X3 LP
F160 Synergy® X3
unique prosthetic solutions
A company of the Bauerfeind Group
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Table of Contents
Related Manuals for uniprox F120 Chopart
Summary of Contents for uniprox F120 Chopart
- Page 1 F140 Pars X3 F150 Synergy® X3 LP F160 Synergy® X3 ORTOTEK A.Ş. Ziya Gökalp Cad. 68/21 Kolej/Ankara/TÜRKEI Distributed by: Uniprox GmbH & Co.KG, H.-Heine-Str.4, 07937 Zeulenroda-Triebes unique prosthetic solutions Ein Unternehmen der Bauerfeind Gruppe – www.uniprox.de A company of the Bauerfeind Group...
- Page 2 2.1 Foot category selection table Please read the IFU carefully before fitting. Only correct usage will To identify the applicable activity level, use the activity table. warrant the function. 1. Intended Use Impact level The carbon prosthetic foot is the basis for the modular design of a leg prosthesis. Activity Level Weight(kg) 2.
- Page 3 2.2.2 Spectra™ Socks If there is mechanical damage to the product, check its function, or contact the • manufacturer or Uniprox. For the highest possible safety and the longest possible service life, the • recommended assembly and usage procedures must be followed.
- Page 4 6.2 Installation Chopart 6.4 Dynamic Alignment The impact energy is stored in the heel spring (except Chopart and Chopart Plus), Position the socket on the sole plate as shown in the illustration, ensuring proper plantar/dorsal flexion and external rotation. The rear third of the Chopart plate must which thus supports the rolling motion.
- Page 5 The product satisfies the requirements of Regulation (EU) 2017/745 of the European Parliament and of the Council (MDR) and bears the CE mark. All major incidents related to the product needs to be informed to Uniprox and/or Ortotek as well as to the competence European Authority.
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