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
2.3 Combination possibilities
This product can be combined with the following Ottobock components:
Adapters
•
4R104=60 double adapter, sliding
•
4R104=75 double adapter, sliding
•
Rotation adapter: 4R57, 4R57=*
•
4R41 lamination anchor with pyramid receiver
•
4R43 lamination anchor with threaded connector
•
4R89 lamination anchor with pyramid adapter
•
4R111=N lamination anchor with threaded connect
or
•
4R111 lamination anchor with pyramid receiver
•
4R116 lamination anchor with pyramid adapter
•
Lamination anchor with pyramid receiver and
angled arm: 4R119
•
4R40 torsion adapter
•
4R118 adapter plate
•
Quickchange: 4R10
Tube adapter
•
AXON tube adapter: 2R20
•
AXON tube adapter with torsion unit: 2R21
Cosmetic cover/protector
•
Foam cover: 3S26
•
4X880=* Genium Protective Cover
Prosthetic feet
The maximum allowable patient weight depends on the foot size.
•
1M10 Adjust
•
1A30 Greissinger plus
•
1C30 Trias
•
1D35 Dynamic Motion
•
1C10 Terion
•
1C40 C-Walk
•
1C60 Triton
•
1C61 Triton Vertical Shock
•
1C62 Triton Harmony
•
1C63 Triton Low Profile
•
1C66 Triton smart ankle
•
1C64 Triton Heavy Duty
•
Triton side flex: 1C68
•
1E56 Axtion
•
1E57 Lo Rider
•
Challenger: 1E95
•
1B1 Meridium
•
Meridium: 1B1-2
•
Empower: 1A1-1
The
1C63 Triton Low Profile
prosthetic foot may only be combined with
this knee joint
in the ranges listed below
(see table).
Please contact Ottobock customer service if you would like a combination outside the approved ranges.
Body weight
Tube adapter
Approved foot size [cm]
up to 125 kg (up to 275 lbs)
2R20, 2R21
21 to 30
126 kg to 150 kg (276 lbs to 330 lbs)
2R20
21 to 28
2.3.1 Combination with an osseointegrated implant system
Only valid for the products 3B1-2/3B1-2=ST
This product can be connected to a socket or to an osseointegrated, percutaneous implant system.
In case of connection to an implant system, verify that the manufacturer of the implant system and the manufactur
ers of the corresponding exoprosthetic components/adapters also permit this combination. It must be ensured that
all indications/contraindications, the field of application, the conditions of use and all safety instructions are com
plied with for the implant system, corresponding exoprosthetic components, corresponding adapters and for the
knee joint.
Among other things, this relates to the body weight, mobility grade, type of activity, load capacity of the implant and
bone anchoring, freedom from pain under functional load and compliance with the permissible ambient conditions
(see Page 103).
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Product description
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