DJO 79-97757 Procare Plantar Fasciitis Splint Instructions
- June 12, 2024
- DJO
Table of Contents
79-97757 Procare Plantar Fasciitis Splint
Instructions
BEFORE USING THE DEVICE, PLEASE READ THE FOLLOWING INSTRUCTIONS COMPLETELY AND CAREFULLY. CORRECT APPLICATION IS VITAL TO THE PROPER FUNCTIONING OF THE DEVICE.
INTENDED USER PROFILE:
The intended user should be a licensed medical professional, the patient, the
patient’s caretaker, or a family member providing assistance. The user should
be able to read, understand and be physically capable to perform all the
directions, warnings and cautions provided in the information for use.
INDICATIONS: Helps alleviate pain associated with plantar fasciitis.
Soft-good/semi-rigid designed to restrict motion through elastic or semi-rigid
construction.
CONTRAINDICATIONS: Do not use if you are allergic to any materials
contained in this product.
WARNINGS AND PRECAUTIONS:
- It is recommended to have the device fitted by a suitably qualified healthcare professional. If you develop an allergic reaction and/or experience itchy, red skin after coming into contact with any part of this device, please stop using it and contact your healthcare professional immediately.
- If pain, swelling, changes in sensation or other unusual reactions occur while using this product, you should contact your doctor immediately.
- Do not use over open wounds.
- Do not use this device if it was damaged and/or package has been opened.
NOTE: Contact manufacturer and competent authority in case of a serious incident arising due to usage of this device.
APPLICATION INSTRUCTIONS:
A) The splint should be applied with the patient seated.
B) Loosen the upper and lower straps and place foot into splint. Ensure
that the heel is securely seated at the back of the splint. (Figure 1)
C) Secure the lower strap first by threading it through the D-ring on the
opposing side of the splint and attach with the contact closure. Secure the
upper strap the same as the lower strap. (Figure 2) Straps should be snug but
not tight. If numbness or tingling occurs while wearing splint, contact your
physician.
D) Both upper and lower straps may be trimmed if necessary for proper
fit. Release the strap from the Y-tab on one side of splint, trim strap to
desired length and reposition for proper fit. Strap pad may be repositioned
for optimum comfort.
E) An athletic sock may be worn on foot for additional comfort.
F) Side straps may be gradually tightened to increase flexion of foot for
rehabilitation.
Toe wedge may be placed at forefoot between liner and boot to provide
additional stretch.
NOTE: This product is not designed for the patient in a weight bearing
situation or everyday ambulation.
USE AND CARE:
- Liner may be removed and hand washed in cold water (86°F/30°C). AIR DRY.
- Shell may be wiped down with damp cloth.
MATERIAL CONTENTS:
Shell – Polypropylene
Pads – Nylon/Polyurethane foam
Binding – Polyester
Hook & Loop – Nylon
Wedge – Polyethylene foam
Sole – EVA textured rubber
WARRANTY: DJO, LLC will repair or replace all or part of the unit and its
accessories for material or workmanship defects for a period of six months
from the date of sale.
FOR SINGLE PATIENT USE ONLY.
NOT MADE WITH NATURAL RUBBER LATEX.
NOTICE: WHILE EVERY EFFORT HAS BEEN MADE IN STATE-OF-THE-ART TECHNIQUES TO
OBTAIN THE MAXIMUM COMPATIBILITY OF FUNCTION, STRENGTH, DURABILITY AND
COMFORT, THERE IS NO GUARANTEE THAT INJURY WILL BE PREVENTED THROUGH THE USE
OF THIS PRODUCT.
CAUTION: FEDERAL LAW (U.S.A.) RESTRICTS THIS DEVICE TO SALE BY OR ON THE
ORDER OF A LICENSED HEALTH CARE PROFESSIONAL.
MDSS GmbH
Schiffgraben 41
30175 Hannover, Germany
DJO, LLC
1430 Decision Street
Vista, CA 92081-8553 • USA
©2020 DJO, LLC
13-1965-0-00000 REV G – 2020-12-02
Read User Manual Online (PDF format)
Read User Manual Online (PDF format) >>