In case of a product malfunction, safety mode makes restricted operation possible. Resistance
parameters that are predefined by the product are configured for this purpose (see Page 58).
The microprocessor-controlled hydraulic unit offers the following advantages
•
Stability while standing and walking
•
Smooth, harmonious, quiet initiation of the swing phase
•
Automatic recognition of sitting down. Manual unlocking of the joint not required.
•
Support while sitting down with individually adaptable resistance. This resistance remains
constant during the entire process of sitting down.
•
Support while standing up. The knee joint can be loaded even before reaching full extension.
•
Approximation of the physiological gait pattern
•
Adaptation of product characteristics to various surfaces, inclines, gait situations and walking
speeds
•
Manual locking of the knee joint for use of a wheelchair (see Page 57). This function makes it
possible to lock the knee joint in any extended position while sitting down. This is particularly
useful in order to keep the foot from dragging on the ground when the user is being transpor
ted in a wheelchair.
3 Application
3.1 Indications for use
The product is to be used solely for lower limb prosthetic fittings.
3.2 Area of application
Our components perform optimally when paired with appropriate components based upon weight
and mobility grades identifiable by our MOBIS classification information and which have appro
priate modular connectors.
This product is recommended for mobility grade 1 (indoor walker) and mobility
grade 2 (restricted outdoor walker). Approved for a body weight of max. 125 kg.
m°
kg
3.3 Conditions of use
The product was developed for everyday use and should not be used for walking speeds over
3 km/h or 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 60).
The prosthesis is intended for use exclusively on the user for whom the adjustment was made.
The manufacturer does not authorise use of the prosthesis on another person.
3.4 Indications
•
For users with knee disarticulation or transfemoral amputation
•
For unilateral or bilateral amputation
•
Dysmelia patients with residual limb characteristics corresponding to knee disarticulation or a
transfemoral amputation
•
The user must fulfil the physical and mental requirements for perceiving optical/acoustic sig
nals and/or mechanical vibrations
3.5 Qualification
The product may be fitted only by qualified personnel authorised by Ottobock after completing the
corresponding training.
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