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FOREWORD
Foreword
Thank You for Purchasing Arjo Equipment.
Your Arjo Strap Stretcher is part of a series of quality products designed especially for your health care facility.
We are dedicated to serving your needs and providing the best products available along with training that will
bring your staff maximum bene
¿
t from every Arjo product. Contact us if you have any questions about the use
or maintenance of your Arjo product.
Customer Contact Information
For questions regarding this product, supplies, maintenance, or additional information about Arjo products and
service, please contact Arjo or an Arjo authorized representative, or visit www.arjo.com.
Please Read and Fully Understand the Instructions for Use (IFU) before Using
the Arjo Strap Stretcher
The information in this manual is crucial to the proper operation and maintenance of the Arjo Strap Stretcher.
It will help protect your product as well as make sure that the equipment performs to your satisfaction. Lifting
and transferring a person always presents a potential risk. Some of the information in this manual is important
for your safety and must be read and understood to help prevent injuries.
A service routine must be performed on your Arjo Strap Stretcher by quali
¿
ed service personnel. This will
ensure the safety and good function of your product. See “Care and Maintenance” section in this manual.
Please contact your local Arjo agent if you need more information, notice any changes in the performance of
your ceiling lift, want to report an unexpected event or need any help in setting up, using or maintaining your
Arjo Strap Stretcher. The agent can offer comprehensive support and service programs to maximize the long-
term reliability, safety and value of the product.
Additional copies of this manual can be provided by your local Arjo agent. When ordering, include the
Instructions For Use manual, product number Arjo Strap Stretcher.
Report Unexpected Operations or Events
Contact your local Arjo representative if any unexpected operations or events occur. The contact information
appears on the last page of this IFU.
Serious Incident
If a serious incident occurs in relation to this medical device, affecting the user, or the resident then the user
or resident should report the serious incident to the medical device manufacturer or the distributor. In the
European Union, the user should also report the serious incident to the Competent Authority in the member
state where they are located.
