DJO Procare Posterior Tibia/Fibular Splint Femoral Leg Splint Instructions

DJO Procare Posterior Tibia/Fibular Splint 
Femoral Leg 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.

INTENDED USE/INDICATIONS:

The Procare Posterior Tibia/Fibular splint and Femoral Leg Splint are designed to provide support and immobilization to the lower leg, ankle and foot. It may be suitable for use following a knee injury, soft tissue injury, ankle fracture or lateral ankle sprain. Providing immobilization or controlled movement of the limb or body segment.

CONTRAINDICATIONS: None.

WARNINGS AND PRECAUTIONS:

It is recommended to have the device fitted by a suitably qualified health care 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 packaging has been opened.

NOTE: Contact manufacturer and competent authority in case of a serious incident arising due to usage of this device.

APPLICATION INFORMATION:

A) Place splint on the leg in the desired position and secure with an elastic wrap, wrapping distal to proximal.

USE AND CARE:

The splint is malleable and can be molded if desired.
The splint is autoclavable.

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.