These sensor data are updated and evaluated 100 times per second. As a result, the behaviour of
the product is adapted to the current motion situation (gait phase) dynamically and in real time.
Thanks to the microprocessor-controlled stance and swing phase, the system can be individually
adapted to your needs.
For this purpose, the product is adjusted by qualified personnel using adjustment software.
The product features MyModes for special motion types (e.g. cross-country skiing, ...). These are
pre-configured by the prosthetist using the adjustment software and can be activated with special
motion patterns, the cockpit app and the remote control (optional accessory) (see Page 27).
In case of a system malfunction, safety mode makes restricted operation possible. Predefined
resistance parameters are configured in the product for this purpose (see Page 38).
Empty battery mode permits safe walking when the battery is drained. Resistance parameters that
are predefined by the product are configured for this purpose (see Page 38).
The microprocessor-controlled hydraulic unit offers the following advantages
•
Approximation of the physiological gait pattern
•
Stability while standing and walking
•
Adaptation of product characteristics to various surfaces, inclines, gait situations and walking
speeds
4 Application
4.1 Indications for use
The product is to be used solely for lower limb exoprosthetic fittings.
4.2 Area of application
Area of application according to the MOBIS mobility system:
The product is recommended for mobility grade 3 (unrestricted outdoor walker)
and mobility grade 4 (unrestricted outdoor walker with particularly high demands).
m°
Approved for a body weight of up to 125 kg (275 lbs).
kg
4.3 Conditions of use
The product was developed for everyday use and must not be used for unusual activities. These
unusual activities include, for example, extreme sports (free climbing, parachuting, paragliding,
etc.).
Permissible ambient conditions are described in the technical data (see Page 48).
The product is intended exclusively for use on one user. Use of the product by another person is
not approved by the manufacturer.
4.4 Indications
•
For users with knee disarticulation, transfemoral amputation and hip disarticulation (users
with hip disarticulation or hemipelvectomy have to be fitted with the 7E10=* Helix
•
For unilateral or bilateral amputation
•
Dysmelia patients with residual limb characteristics corresponding to knee disarticulation,
transfemoral amputation or hip disarticulation
•
The user must fulfil the physical and mental requirements for perceiving optical/acoustic sig
nals and/or mechanical vibrations
4.5 Qualification
The product may be fitted only by qualified personnel authorised by Ottobock after completing the
corresponding training.
8 | Ottobock
3D
hip joint).