EN
Contraindications
If the following symptoms exist, the orthosis should
only be worn after consultation with the physician:
pronounced varus or valgus deformity, lymph drain-
age disorders, arterial flow impairment, post-throm-
botic syndromes, all forms of varicosity, ulceration,
recent or recurring flebothrombosis, permanent
oedema of the lower leg, skin diseases or skin irrita-
tions; Wounds in the treatment area are to be covered
with sterile dressings, a below-knee compression
stocking (AD) should also be worn by elderly patients
with a tendency towards swelling and in conjunction
with varicosity.
The Julius Zorn 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 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 orthosis can be disposed of through normal
waste channels. No special waste disposal require-
ments apply.