darco GentleStep Guia De Inicio Rapido

Manufactured for:
DARCO® International, Inc.
810 Memorial Blvd.
Huntington, WV 25701, USA
Phone 304.522.4883
www.darcointernational.com
DARCO® (Europe) GmbH
Gewerbegebiet 18
82399 Raisting, Germany
Telefon +49 8807 9228 0
www.darco.de
Made in China GS-IFU-21_Rev0321
®
GentleStep™
Instructions For Use
EN
Indications
> Patients diagnosed with diabetes
> Peripheral neuropathy
> Bony abnormalities of the foot
Contraindications
> Open fractures
Cleaning Instructions/Maintenance
> When the shoe is slightly dirty, clean it with a damp cloth or a soft brush.
> For heavily soiled shoes, machine wash on gentle cycle or handwash in mild detergent.
> Allow the shoe to air dry only.
Instructions for use
The special fitting mark located on the side of the sole assists in the proper fitting of the
shoe. The ball of the foot or big-toe joint should be located at or just behind this marker. Correct
fitting is essential to receiving maximum benefit from this professionally-designed shoe.
1. Open the shoe by means of the closures.
2. Please ensure that the foot is properly positioned in the shoe.
3. Secure the foot in the shoe with the closures.
Caution
Please always follow these instructions for use. In case of pain or swelling, discontinue use and
consult your medical provider immediately. This device is designed to assist recovery and should
be used exclusively under the instruction of and in consultation with a healthcare professional.
DARCO® International Inc. does not assume any responsibility for misuse of the product. It is
advisable to wear dressings or socks with the shoe. Do not drive a vehicle while you are wearing
this device. Use extreme caution when walking on all surfaces when using this device. Walk
more slowly than normal. This shoe is designed to be worn in pairs. This device is for single-pa-
tient use only.
To the patient/user: This device has been designed and manufactured by DARCO® International,
Inc. to be state of the art for treatment of a specific medical condition. Should any serious incident
occur in relation to this device it should be reported to the manufacturer at the contact infor-
mation listed on this document and the proper authority of the country or state where you are
located. When treatment is complete, dispose of this device according to local laws and ordinances.