Entsorgung
Im Regelfall ist das Produkt nach Nutzungsende über
den herkömmlichen Entsorgungsweg zu vernichten.
Bitte beachten Sie dabei die geltenden örtlichen /
nationalen Vorgaben.
EN
Intended purpose
The JuzoPro Cervical Collar Supports stabilise the
cervical spine thanks to their contours and potential
reinforcing elements.
This is how to put on your
JuzoPro Cervical Collar Support correctly:
1. Open the orthosis fully and place it around your
neck so that the fastener (velcro strap) is located at
the back of your neck. When it is positioned correct
ly, your chin should be embedded in the opening
(recess) provided for it.
2. The orthosis is especially designed for easy adjusta
bility so you can accommodate the right tightness to
help stabilise the neck, and prevents restriction. You
can readjust it at any time if necessary. Caution:
rough, unfiled finger nails or sharpedged rings etc.
may damage the material.
Please note:
Only wear your orthosis when prescribed by your
physician. Medical aids should only be dispensed by
suitably trained staff of a medical products supplier.
The orthosis can only be fully effective when it has
been put on correctly and is being worn in accordance
with treatment recommendations. The orthosis is
largely resistant to oils, creams, skin moisture and
other environmental influences. Certain combinations
may negatively impact on the durability of the fabric.
We therefore recommend that it gets examined
regularly by the medical products supplier. Should
the product become damaged, please consult your
specialist supplier. Do not repair the orthosis yourself –
this could compromise its quality and medical efficacy.
For hygienic reasons, the orthosis is not suitable for
treating more than one patient. The sewnin textile
label is important for the identification and traceability
of the product. We therefore ask you not to remove the
label under any circumstances.
Washing and care instructions
Please observe the care instructions on the textile label
attached to your orthosis. Wash the orthosis separately
the first time (the colour might come out). Close the
touch fastener and handwash the orthosis with laundry
detergent for delicate fabrics every day or between uses
at approx. 30 °C. We recommend using the mild
Juzo Special Detergent for this. Afterwards, please
rinse out the orthosis well and allow it to dry at room
temperature. To reduce the drying time, you can place
the orthosis on a thick terry towel and pat it dry. Do not
leave in the towel and do not place on a heater or in the
sun to dry. The orthosis is not suitable for tumble drying.
This Juzo product must not be cleaned chemically.
Material composition
The exact details can be found on the textile label on
your orthosis.
Storage information and usage duration
Store in a dry place and protect from sunlight. The
medical retailer or doctor prescribing the orthosis will
advise on exactly how long it can be used for.
Indications
Cervical syndrome, whiplash, torticollis, posttraumatic
pain, osteochondrosis (degenerative change), spondy
larthrosis (wear of the cervical spine)
Contraindications
If the following symptoms exist, the orthosis should
only be worn after consultation with the physician:
tracheostomy, hypersensitivity in the neck area,
severe swelling, skin disorders or skin irritations; Open
wounds in the treated area should be kept sterile.
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
directed. However, if negative alterations (such as for
example skin irritations) should occur whilethe 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 symptoms worsen
during the time you are wearing the product, please
take off the orthosis and consult a medical specialist
immediately. The manufacturer is not liable for dam
ages / injuries which have been caused by improper
handling or misuse.
In the event of complaints related to this product,
such as damage to the material or problems with the
fit, please contact the medical retailer directly. Only
serious 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 authori
ty in the Member State. Serious incidents are defined in
Article 2 (65) Regulation (EU) 2017 / 745 (MDR).
Disposal
As a rule, the product is to be destroyed via the con
ventional disposal route after the end of use. Please
observe the applicable local / national regulations.