Contraindications - Juzo Pro Lumbal Xtec Strong Gebrauchsanweisung

Material composition
Details are provided on the label sewn into your
orthosis.
Notes for the orthopaedic technician
The stabilisation rods can be adjusted to the indivi-
dual requirements of the patient.
JuzoPro Lumbal Xtec Strong: To shape the rods or,
depending on the indication, remove them comple-
tely, simply take them out of the pockets.
JuzoPro Lumbal Xtec Plus: The orthosis can be
dismantled simply by detaching the pad and strap
element.
Storage information
Store in a dry place and protect from sunlight.
Indications
JuzoPro Lumbal Xtec Strong:
joint wear (facet joint arthrosis), severe pain and
irritation in the lumbar region (lumbalgia / lumboi-
schialgia), painful bulging of the discs in the lumbar
region (protruded / prolapsed disc), pain in the lum-
bosacral junction, breaking of the connection bet-
ween two vertebrae (spondylolysis) guarantee since
above-average product quality has always been a
tradition at Juzo, degenerative vertebral slippage
(degenerative spondylolisthesis/1st degree with lum-
balgia), deterioration in posture (myostatic muscular
insufficiency / segment instability), sudden onset of
pain followed by restriction in movement (lumba-
go / with sacroiliac joint involvement), constriction of
the spinal canal (lumbar spinal canal stenosis)
JuzoPro Lumbal Xtec Plus:
severe persistent / recurrent pain in the lumbar regi-
on (chronic, recurrent lumbalgia / ligamentosis), joint
wear (osteochondrosis / spondylosis / spondylar-
throsis), mild pain and irritation in the lumbar region
(lumboischialgia / radiculopathy), breaking of the
connection between two vertebrae (spondylolysis),
mild to moderate malformation in the lumbar region
(lumbar deformity)

Contraindications

In case of the following syndromes or clinical pic-
tures, the orthosis should only be worn after prior
consultation with the treating physician:
∙ skin diseases or skin irritations;
Wounds in the treatment area are to be covered
with sterile dressings.
The Julius Zorn GmbH Group assumes no liability as
a result of any contraindicated use of this product.
Side effects
There are no known side effects when used as di-
rected. However, if negative alterations (such as for
example skin irritations) should occur while the use
of our products has been prescribed, please go to
your physician or your specialist dealer immedia-
tely. If an incompatibility should be known against
one or several ingredients of this product, please
check back with your physician before use. If your
medical condition deteriorates while the use of our
products, please go to your physician immediately.
The manufacturer is not liable for damages / injuries
which have been caused by improper handling or
misuse.
In the case of complaints related to this product,
such as damage to the knitted fabric or problems
with the fit, please contact the medical retailer di-
rectly. Only serious incidents that may lead to a ma-
jor deterioration of the patient's medical condition
or to death should be reported to the manufacturer
and the relevant authority in the Member State. Seri-
ous incidents are defined in Article 2 (65) Regulation
(EU) 2017/745 (MDR).
Disposal
Your orthosis can be disposed of through normal
waste channels. No special waste disposal require-
ments apply.
EN