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Idiomas disponibles
Idiomas disponibles
1Н08А
Articulated foot with shock absorber and heel adjustment
INSTRUCTIONS FOR USE AND MAINTENANCE
Dear Customer,
Please read the instructions carefully. Make sure that the user understands the instructions
for use, paying particular attention to the safety and maintenance warnings.
APPLICATION
The 1Н08А articulated foot has been designed for patients with unilateral or bilateral fem-
oral amputation at different levels or tibial proximal, transtibial or distal amputation. It can
also be used in prostheses after knee or hip disarticulation. The prosthesis is made for the
right and left foot. The foot has two fixed heel height positions.
TECHNICAL CHARACTERISTICS
Code
Foot dimensions
Foot length, mm
Articulated foot weight, g
Rigidity of the fitted shock
absorber
For patients weighing
Foot heel height (without shoes)
on the supporting surface
Temperature range for use
Angular adjustment of the whole
prosthesis on the frontal and
sagittal planes
Warranty period
DESCRIPTION OF THE STRUCTURE
The 1Н08A articulated foot consists (see Fig. 1) of support element 1, socket 2 with safety
12, limiter 9 and cosmetic cover 3 made from microcellular polyurethane, housing 7, joint 4,
washer 5, nut 6, nut 11 and disc 10.
1
5
Main body
Washer
2
6
Socket
Nut
3
7
Cosmetic cover
Housing
4
8
Joint
Shock absorber
ORLIMAN S. L. U.
C/ Ausias March, 3 - Pol. Ind. La Pobla-L´Eliana · Apdo. de correos 49
C.P.: 46185 - La Pobla de Vallbona Valencia - España (Spain)
Tel.: +34 96 272 57 04 - Fax: +34 96 275 87 00 - Exports Tel.: +34 96 274 23 33
E-mail: orto@orliman.com · Exports email: export@orliman.com - www.orliman.com
LB-I-1Н08А
EDITION: 05/2015
1H08A
22
23
24
25
26
27
28
220
230
240
250
260
270
280
527
557
587
617
667
697
717
±10
±10
±10
±10
±10
±10
±10
soft (S)
normal (N)
up to 100 kg
Position 1 - 25 mm
Position 2 - 10 mm
From -40 °C to +40 °C
not less than ±7.5°
2 years
9
Limiter
10
Disc
11
Nut
12
Safety
The kit for attaching the 2Н04А/1 articulated ankle joint includes a set of rubber shock
absorbers 8 with different degrees of rigidity (soft, normal and rigid), marked respectively
with the letters S, N and R.
The articulated ankle joint is attached through the hole in the prosthetic foot and fixed into
place using nut 6 and safety washer 5.
Prosthetic feet with sizes 22, 23 and 24 come with a soft (S) shock absorber 8; all other
feet come with normal (N) rigidity shock absorbers 8. Should the customer request the re-
placement of shock absorber 8 with one of different rigidity (S, N or R), it will be supplied
additionally. Ref 304242/2S (soft); Ref 304242/2H (hard).
The articulated foot is compatible with Orliman's modular lower-limb prosthetic systems.
OPERATION
During the stance phase (forward impulse) of the gait cycle and under the weight of the
body, shock absorber 8 is compressed and the forefoot drops onto the supporting surface.
This ensures a more stable gait with the prosthesis. During the gradual transition towards
29
30
the end of the stance phase (backward impulse), the deformation of the forefoot (tip of the
290
300
foot) takes place.
To change the heel height, shock absorber 8 should be compressed by removing the load of
757
817
limiter 9 and, through the foot's side holes, move limiter 9 to the stop in fixed position 1 or 2.
±10
±10
ADJUSTMENT
Adjustment of the articulated foot is carried out by putting limiter 9 into position 1.
Changing the rigidity of the heel is carried out by replacing shock absorbers 8 with others
that have a different rigidity. Depending on the patient's weight, it is recommended to use
the shock absorbers in the following way:
- up to 70 kg - soft (S) or normal (N)
- up to 100 kg - normal (N) or rigid (R)
To replace shock absorber 8, unscrew screw 11, replace the shock absorber, insert disc 10
and tighten nut 11 within the limits of dimension B.
It is also possible to adjust the rigidity of the heel. The degree of compression of shock ab-
sorber 8 can be adjusted by screwing or unscrewing screw 11 within the limits of dimension B.
MAINTENANCE
During use or cleaning, do not use talcum powder. Do not put the product into contact with
corrosive or abrasive elements such as fresh or salt water, acids, dust, sand or other sub-
stances.
At least once a year, have the product checked by an orthopaedic technician for proper op-
eration and wear. If you detect any unusual changes in the product's functioning or hear it
making noises, stop using it immediately and notify an orthopaedic technician.
RECOMMENDATIONS - WARNINGS
These products should not be used for purposes other than those described in these instruc-
tions. They should only be used by one person and under the conditions prescribed.
Before use, the product must be adapted by an orthopaedic technician.
When disposing of the product and packaging, strictly comply with the refuse disposal reg-
ulations of your community.
In knee joints, there is risk of entrapment, use caution.
As the product features metal components, use caution in the case of magnetic resonance.
WARRANTY
These products comply with European Medical Devices Directive 93/42/EEC (Spanish Royal
Decree 1591/2009). They have undergone tests in accordance with international standard
EN ISO 22523 for prostheses and orthoses and EN ISO 10328 for lower-limb prostheses.
ORLIMAN, S.L.U. guarantees all of its products, provided that they have not been tampered
with or altered from their original form. The company does not guarantee products whose
characteristics have been altered through any kind of misuse, breakage or defect. If you
notice any defect or abnormality, notify the supplier immediately in order for the product
to be replaced.
WARRANTY
years from purchase
Reference
Signature and stamp of the
orthopaedic establishment
Batch
Date of
no.
purchase
For the warranty to be valid, it is
necessary to complete these details.
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