Proprietary Notice - Ferno Viper Stretcher Instructions For Use Manual

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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 your local Ferno distributor
or 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.
2
VIPER
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
To request additional free users' manuals,
contact Ferno Customer Relations, your Ferno
distributor, or www.ferno.com.
Product Name/Model
Date of Manufacture
Unique Device Identification (UDI)
Ferno complies with the United States Food and Drug Administration's
(FDA), MDA & CE Unique Device Identification (UDI) regulation to
identify medical devices. The UDI label contains information in human-
and machine-readable form, which includes the serial number, date of
manufacture and Product name. The label is located on the stretcher
as per the photo above
frame
MEDIROL s.r.o.
Na Strži 126/4
140 00 Prague, Czech Republic
USERS' MANUALS
Manufacturer
Date
Serial Number
© Ferno / May 2023, Rev 1

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