Ferno Customer Relations; Unique Device Identification (Udi) - Ferno iNSX Integrated Patient Transport & Loading System Instructions For Use Manual

Ferno Customer Relations

For ordering assistance or general information:
CANADA AND THE U.S.A.
Telephone (Toll-free)
Telephone
Fax (Toll-free)
Fax
Internet
ALL OTHER LOCATIONS
For assistance or information, please contact your Ferno distributor. If you do not
have a Ferno distributor, please contact Ferno Customer Relations:
Ferno-Washington, Inc., 70 Weil Way
Wilmington, Ohio 45177-9371, U.S.A.
Telephone
Fax
Internet
Disclaimer
This manual contains general instructions for the use, operation and care of this
product. The instructions are not all-inclusive. Safe and proper use of this product
is solely at the discretion of the user. Safety information is included as a service
to the user. All other safety measures taken by the user should be within and
under consideration of applicable regulations and local protocol. Training on
the proper use of this product must be provided before using this product in an
actual situation.
Retain this manual for future reference. Include it with the product in the event
of transfer to new users. Additional free copies are available upon request from
Customer Relations.
Proprietary Notice
The information disclosed in this manual is the property of Ferno-Washington,
Inc., Wilmington, Ohio, USA. Ferno-Washington, Inc. reserves all intellectual
property rights, proprietary design rights, manufacturing rights, reproduction
use rights, and sales use rights thereto, and to any article disclosed therein
except to the extent those rights are expressly granted to others or where not
applicable to vendor proprietary parts.
Limited Warranty Statement
The products sold by Ferno are covered by a limited warranty, which is printed
on all Ferno invoices. The complete terms and conditions of the limited warranty,
and the limitations of liability and disclaimers, are also available upon request by
calling Ferno at 1.800.733.3766 or 1.937.382.1451.
Adverse Event Notice
In the event of an adverse event or serious incident related to the use of this
device, the end user/operator must report the incident to Ferno-Washington,
Inc. at 70 Weil Way, Wilmington, Ohio 45177 USA, 1-877-733-0911, or via email at
tscoordinator@ferno.com. If the incident occurred in the European Union, report
it to Ferno's Authorized EU Representative and the competent authority of the
Member State in which the end user is established.
Battery Recycling
In the U.S.A., contact TerraCycle Regulated Waste to responsibly recycle and
dispose of the Ferno 36VDC Lithium-iron phosphate battery. Visit
tcrwusa.com/.
Outside the U.S.A., contact the government of your country for recycling
information. See "Recycling Notice" on page 39.
2
iN∫X®
1.877.733.0911
1.937.382.1451
1.888.388.1349
1.937.382.1191
www.ferno.com
Country Code +1.937.382.1451
Country Code +1.937.382.6569
www.ferno.com
https://
To request additional free users' manuals,
contact Ferno Customer Relations, your Ferno
distributor, or www.ferno.com.
Product Name/Model
Date of Manufacture
SN
Serial Number
Ferno-Washington Inc. | Wilmington, Ohio 45177 USA | +1.937.382.1451
Manufacturer

Unique Device Identification (UDI)

Ferno complies with the United States Food and Drug Administration's (FDA)
Unique Device Identification (UDI) regulation to identify medical devices.
The UDI label contains information in human- and machine-readable form.
Device information is online at the FDA's Global Unique Device Identification
Database (GUDID). The public can search and download information at
AccessGUDID at www.fda.gov.
The label is located on the under the battery, on the battery tray.
USERS' MANUALS
Serial Label
(01) Global Trade Item Number
(11) Date of Manufacture
(21) Serial Number
GS1 Data Matrix
© Ferno / 234-3622-09 / December 2022