EN
Material composition
For precise details, please see the textile label sewn into
your compression garment.
Storage information and shelf life
Store in a dry place and protect from sunlight. Standard
products have a maximum shelf life of 36 months. The com-
pression garment then has a usage period of 6 months.
The usage period depends on correct handling (e.g. care,
donning and doffing) and normal use of the products. The
usage period of the medical product is printed on the box
with an hourglass symbol. Custom-made products are for
immediate use. Body measurements may change based on
the patient’s condition and individual circumstances. Cus-
tom-made products are therefore designed for a usage
period of 6 months. After the 6-month usage period, body
measurements must be re-checked by a medical special-
ist. In the event of significant changes in measurements
of the body part that is being treated (e.g. based on ther-
apeutic success, weight change), re-measurement and
supply of a new product may be required earlier, before
the 6-month usage period comes to an end.
Indications
·
treatment of Ulcus cruris venosum type ulcers as an
alternative or complement to compression bandages
following oedema reduction
·
prevention of recurrent Ulcera cruris venosa (recidive
prophylaxis).
Following burns and for scar treatment, we recommend
using our special scar therapy products.
Absolute contraindications
Peripheral artery disease (PAD) stage III/IV, decompensat-
ed heart failure, septic phlebitis, phlegmasia cerulea do-
lens, acute erysipelas, acute bacterial, viral or allergic in-
flammation, untreated or advanced skin diseases/contact
dermatitis, untreated open wounds, swelling of the ex-
tremity of unknown cause, untreated malignant tumours.
Relative contraindications
Pronounced weeping dermatoses, malignant lymphoede-
ma, peripheral artery disease (PAD) stage I/II, peripheral
neuropathy in association with diabetes mellitus, sensory
disorders of the extremities, compensated heart failure,
skin infections, skin diseases (e.g. blistering dermatoses),
intolerance to pressure or the ingredients of the product,
rheumatoid arthritis. If there are open wounds in the area
to be treated, the affected area must be covered with an
appropriate wound dressing or bandage before the com-
pression garment can be applied. Liability for failure to
comply with these contraindications cannot be accepted
by the Julius Zorn GmbH Group.
Side effects
There are no known side effects when used as directed.
However, if negative reactions (such as for example skin
irritations) should occur while the use of our products has
been prescribed, please go to your doctor or your spe-
cialist dealer immediately. If an incompatibility should be
known against one or several ingredients of this product,
please check back with your doctor before use. If your
medical condition deteriorates while using our products,
please go to your doctor immediately. The manufacturer 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 deterioration of the pa-
tient’s medical condition or to death should be reported to
the manufacturer and the relevant authority in the Member
State. Serious incidents are defined in Article 2 (65) Regu-
lation (EU) 2017/745 (MDR).
Disposal
You can dispose of your compression garments in the usu-
al way. There are no specific disposal instructions.
* The Juzo Ulcer System Add set (replacement set) contains only the
liner stockings and is available in medical supply stores.
Summary of Contents for Ulcer System
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