Indications
sprains / strains (medium to severe distortions), inju-
ries of joints / tendons (luxations), tendinous synovitis
(medium to severe tendovaginitis), paralysis / wrist
drop (radial paresis), carpal canal syndrome, chronic
irritative conditions (arthrosis and rheumatoid arthri-
tis), plaster cast substitute (posttraumatic / post-oper-
ative immobilisation)
Contraindications
If the following symptoms exist, the orthosis should
only be worn after consultation with the physician:
lymph drainage disorders, arterial flow impairment,
post-traumatic conditions, skin disorders or skin irri-
tations; Wounds in the treatment area are to be cov-
ered with sterile dressings.
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 doctor immediately. The manufac-
turer 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 fabric or problems with the fit,
please contact the medical retailer directly. Only se-
rious incidents that may lead to a major deterioration
of the patient's medical condition or to death should
be reported to the manufacturer and the relevant au-
thority in the Member State. Serious incidents are de-
fined 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