Gima STICK User guide

PROFESSIONAL MEDICAL PRODUCTS
STICK WITH SEAT
ENGLISH
All serious accidents concerning the medical device supplied by us must be reported to the manufacturer and compe­tent authority of the member state where your registered ofce is located.
INTRODUCTION
Stick with seat, made of aluminium which is light and resistant. The tip is covered with non-slip rubber.
SAFETY RULES
Always contact your specialist dealer to learn how to use it appropriately.
Do not store outdoors, do not expose it to prolonged periods of sunlight. Always move slowly, taking small steps to ensure that the weight distribution is even and that the posi-
Do not use on slippery surfaces (wet oors, snow, ice) or on stairs.
Do not use for purposes other than those for which this product has been designed. Always comply with the weight limits indicated on the label or in the instructions. Use only original tips for repairs.
Only qualied personnel are authorised to repair this item. Should you not use the device for long periods of time, have it checked by your specialist dealer.
Use caution when using on unstable and uneven ground. Check the wear of the non-slip rubber and replace it if necessary.
USE
To sit down, slide the chair from top to bottom.
MAINTENANCE
The product must be cleaned regularly with a clean and dry cloth. The handle must be cleaned with a neutral detergent (do not use corrosive products). The ends must be checked and changed regularly in case of wear.
GIMA WARRANTY TERMS
The Gima 12-month standard B2B warranty applies.
Product code Consult instructions for use Manufacturer
Lot number
Keep in a cool,
dry place
Keep away from sunlight
FS911L (43060)
Foshan Dongfang Medical Equipment Manufactory (LTD.)
5 Xingfu Road, Zone A, Shishan Industrial Park, Nanhai District, Foshan City, China, 528000
Made in China
MedNet EC-Rep GmbH
Borkstrasse 10. 48163 Muenster. Germany
Importato da / Imported by:
Gima S.p.A.
Via Marconi, 1 - 20060 Gessate (MI) Italy gima@gimaitaly.com - export@gimaitaly.com
www.gimaitaly.com
M43060-M-Rev.1-10.21
Medical Device compliant
with Regulation (EU) 2017/745
Caution: read instructions
(warnings) carefully
Authorized representative
in the European community
Medical Device
Date of manufacture
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