pad with firm and comfortable com-
pression. If necessary, adjust the
band closest to the toes to firm and
comfortable compression. Adjust the
ankle band if any gaps or pressure
points occur. The ankle-band should
overlap with the circaid leg garment.
Note: The ankle band may pull from a
different side depending on which foot,
left or right, the garment is applied to.
• Readjust the bands as necessary
throughout the day to maintain a
firm and comfortable compression
level.
Individualisation
This product is not designed to be cut
or modified except as outlined in the
directions for use. The circaid juxtafit
premium ankle foot wrap can be tailo-
red to fit the patient´s foot size and
contour. The ankle foot wrap should be
fitted by a medical professional. Doing
other than instructed will void the
three month limited warranty. The fol-
lowing steps will permanently reduce
the foot-length of the circaid juxtafit
premium ankle foot wrap. The afw can
be trimmed by up to 1.25 in. (3 cm) (see
notches on both sides).
Foot-length
adjustment
circaid juxtafit premium ankle foot
wrap
• With the beige side facing up, mark
the desired length.
• Draw a straight line connecting the
notches.
• Carefully cut along the drawn line,
assuring that the reinforced seam
section of the Velcro material is not
cut.
Care instructions
The garment can be machine washed
using a gentle cycle and dried on a low
heat setting. We recommend using a
laundry bag. To extend the life of the
garment, hand wash and drip dry.
Delicates wash cycle
Do not bleach
Tumble dry, low heat
Do not iron
Do not dry clean
Do not wring
Storage instructions
Keep the product in a dry place and do
not expose to direct sunlight.
6
Lifespan
3 months - due to material wear-and-
tear the medical efficacy can only be
expected for a defined lifespan. This
assumes correct handling of the
garment (e.g. proper care, application,
and removal).
Material composition
Polyurethane, Nylon, Elastane, Polye-
thylene
Disposal
The product can be disposed
of in the domestic waste.
In the event of any complaints
regarding the product such as damage
to the fabric or a fault in the fit, please
report to your specialist medical retailer
directly. Only serious incidents which
could lead to a significant deterioration
in health or to death are to be reported
to the manufacturer or the relevant
authorities in the EU member state. The
criteria for serious incidents are defined
in Section 2, No. 65 of the Regulation
(EU) 2017/745 (MDR).
FRANCAIS / FRENCH
circaid
of
the
premium foot options
Utilisation prévue
Le système d'enveloppement du pied
est un dispositif prévu pour un seul pa-
tient, réutilisable, non invasif et non
stérile, destiné à assurer la compressi-
on du pied et de la cheville chez les pa-
tients atteints de troubles veineux et
lymphatiques.
Indications
• Lymphoedème
• Autres formes d'oedèmes
• Lipoedème
• Insuffisance veineuse chronique
• Varices
• Thrombose veineuse profonde/
• Thrombose veineuse profonde aiguë
• Syndrome post-thrombotique
• Ulcères veineux de stase
• Suites de sclérothérapie
• Lipodermatosclérose
Contre-indications
• Maladie artérielle périphérique sévère
• Insuffisance cardiaque congestive
• Phlébite septique
juxtafit
®
Prévention de la thrombose
non contrôlée
®