Side Effects - Juzo JUZOFLEX Epi Xtra Manual De Instrucciones

Material used
Details are provided on the label sewn into your wrist
support.
Storage information and shelf life
Store in a dry place and protect from sunlight. Sup-
ports have a maximum shelf life of 42 months. The
usage period of the medical product is printed on the
box with an hourglass symbol. Body measurements
may change based on the patient's condition and
individual circumstances. We therefore recommend
that medical specialists check body measurements
regularly.
Indications
tennis or golfer's arm (lateral / medial epicondylitis),
joint effusion / swelling due to joint degeneration or
inflammation (arthritis / arthrosis), sprained elbow
(elbow luxation), persistent soft tissue irritation fol-
lowing an injury / operation (chronic / posttraumatic /
postoperative), sprains / strains (distortions)
Contraindications
If the following symptoms exist, the support should
only be worn after consultation with the physician:
lymph drainage disorders, arterial flow impairment,
post-thrombotic conditions; arterial flow disorder,
post-traumatic conditions, skin disorders 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 of your specialist dealer immediately.
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 manu-
facturer 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 directly. Only
serious incidents that may lead to a major deterio-
ration of the patient's medical condition or to death
should be reported to the manufacturer and the rele-
vant authority in the Member State. Serious incidents
are defined in Article 2 (65) Regulation (EU) 2017/745
(MDR).
Disposal
Your support can be disposed of through normal
waste channels. No special waste disposal require-
ments apply.
EN