Disclaimer Of Warranty And Limitation Of Remedy - Flex Vessel Prep FSC 4-120 Mode D'emploi

X. REFERENCES
The physician should consult recent literature on
current medical practice
preparation, arterial scoring, balloon dilatation and
PTA procedures.
XI. SAFE DISPOSAL INFORMATION
After use, discard the device in accordance with local
environmental regulations for biohazard material.
XII: REPORTABILITY
Report any serious incident that has occurred in
relation to the FLEX Vessel Prep System to
VentureMed Group via contact information specified
below and the authority having jurisdiction in locale.
Revision Details
P eCopy of IFU available on VentureMed website
Q Updated to include any residual risks per Regulation (EU) 2017/745 Annex I
Chapter III, 23.1 (g)
R Incorporate new 75cm length - orderable number FSC 4-75
100073 Revision R
XIII. DISCLAIMER OF WARRANTY AND LIMITATION
OF REMEDY
regarding vessel
There is no expressed or implied warranty, including
any implied warranty of merchantability or fitness for
a particular purpose, on the FLEX VP
described
circumstances shall VentureMed Group be liable for
any direct, incidental or consequential damages
other than as expressly provided by specific law. No
person has the authority to bind VentureMed Group
to any representation or warranty except as
specifically set forth herein.
Descriptions or specifications in VentureMed Group
printed material, including this publication, are
meant solely to generally describe the product at the
time of manufacture and do not constitute any
express warranties.
VentureMed Group, Inc., assumes no liability with
respect to instruments reused, reprocessed or re-
sterilized.
VentureMed Group, Inc.
2800 Campus Drive, Suite 50
Plymouth, Minnesota 55441
US
763-951-0280
www.venturemedgroup.com
MedNet EC-REP GmbH
Borkstraße 10
48163 Münster, Germany
Revision History
Date of Issue: 2022-06
in this publication.
Date
2022-02
2022-06
2022-06
Page 8 of 8
®
product(s)
Under no