Storage Information - Juzo Pro Manu Xtec Palmar Manual De Instrucciones

Materials used
For full details, please refer to the label on the inside
of the product.
Notes for the orthopaedic technician
The integrated stabilising splints have been anatom-
ically preshaped and can be reshaped if necessary.

Storage information

Store in a dry place and protect from sunlight.
Indications
∙ sprains / strains (medium to severe distortions)
∙ injuries of joints / tendons (luxations)
∙ tendinous synovitis (medium to severe tendo-
vaginitis)
∙ paralysis / wrist drop (radial paresis)
∙ carpal canal syndrome
∙ chronic irritative conditions (arthrosis and rheuma-
toid arthritis)
∙ plaster cast substitute (posttraumatic / post-opera-
tive 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 using this
product correctly. However, if you notice any adverse
changes (e.g. irritation of the skin) during the pre-
scribed use, please consult your doctor or medical
retailer immediately. If you know that you are allergic
to one or more of the product ingredients, please
consult your doctor before using the product. The
manufacturer does not accept any liability for dam-
age/injuries resulting from improper use 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.
EN