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Idiomas disponibles
7Н08А
Hole lock
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 hole lock is used in tibial and femoral prostheses and is designed to fix the silicone liner
to the socket, ensuring secure fastening of the prosthesis to the patient's stump without any
additional fastening.
TECHNICAL CHARACTERISTICS
Code
Housing material
Bushing and grooved pin material
Item weight
For patients weighing
Temperature range for use
Distance between the two pairs of rows of
M6 holes for fastening the DCR
Warranty period
DESCRIPTION OF THE STRUCTURE
The hole lock consists of housing 1 (Fig. 1), pin 2, bushing 3, extension 8 and the locking
mechanism. The locking mechanism consists of mechanism housing 4, gear axis 5, free
coupling 9, spring 6 and bushing 7.
To prevent the hole lock from unscrewing from housing 1, it features installation screw 11.
The hole lock kit also includes screws 10 for fastening to the socket.
Socket 8 has an M10 thread for connection to the other components of the hole lock.
The hole lock features four M6 holes for fastening the socket support to other compatible
lower-limb prosthetic systems made by other manufacturers.
2
3
1
1
Housing
2
Grooved pin
3
Bushing
4
Locking mechanism housing
5
Gear axis
6
Spring
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-7H08A
EDITION: 05/2015
7Н08А
Aluminium
Stainless steel
185 g
up to 125 kg
From -40 °C to +40 °C
36 mm
2 years
11
5 9
4
6
7
10
7
1 unit
Bushing
8
1 unit
Extension
9
1 unit
Free coupling
10
1 unit
Screw
11
1 unit
Installation screw
1 unit
FITTING THE ITEM TO THE PROSTHESIS
The fitting of the hole lock is carried out with the 4 screws 10. Screw tightening torque - 6
Nm.
When fitting the hole lock to the prosthesis, it is possible to shorten extension 8 to the area
free of grooves.
OPERATION
To fit the prosthesis, it is necessary to insert the stump with the silicone liner (and pin 2
fastened to it) into the socket. In this case, fixing is automatic when pin 2 attaches to gear
axis 5.
If pin 2 has to be adjusted, it is necessary to turn extension 8 clockwise.
To remove the prosthesis, it is necessary to press extension 8 to the stop, which releases pin
2 from its connection to gear axis 5, and then remove the stump from the liner.
If it is necessary to loosen the locking mechanism, unscrew installation screw 11 with the
2.5 mm Allen key.
ADJUSTMENT AND MAINTENANCE
During the period of use, no adjustment is necessary. All settings are carried out at the
factory.
In order for the lock to function reliably for a long time, it is desirable to prevent it from be-
coming dirty, particularly clogging by sand or other particles, which causes increased wear.
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.
8
1 unit
1 unit
1 unit
4 unit
1 unit
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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