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Cordis PRECISE Gebrauchsanleitung Seite 8

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d. Select an appropriate size PTA balloon catheter and
dilate the stricture with conventional technique. The
inflation diameter of the PTA balloon used for post
dilatation should approximate the diameter of the
reference biliary duct. Remove the PTA balloon from the
patient.
7.
Post Stent Placement
a. Remove the guidewire and sheath from the body.
b. Close entry wound as appropriate.
c. Discard the delivery system, guidewire and sheath.
NOTE: Physician experience and discretion will
determine the appropriate drug regimen for each
patient.
IX. MRI Compatibility
The stent is MRI safe and does not interfere with, nor is affected
by, the operation of an MRI device.
X.
How supplied
The Cordis PRECISE Nitinol Stent Transhepatic Biliary System is
supplied sterile (by ethylene oxide gas) and is intended for ONE
USE ONLY.
References
1
"MRI Imaging Artifacts, Ferromagnetism, and Magnetic Torque of Intravascular Filters Standard Coils," Radiology 1988 166:657-664
8
1
DISCLAIMER OF WARRANTY AND LIMITATION OF
REMEDY
THERE IS NO EXPRESS OR IMPLIED WARRANTY,
INCLUDING WITHOUT LIMITATION ANY IMPLIED
WARRANTY OF MERCHANTABILITY OR FITNESS FOR A
PARTICULAR PURPOSE, ON THE CORDIS PRODUCT(S)
DESCRIBED IN THIS PUBLICATION. UNDER NO
CIRCUMSTANCES SHALL CORDIS BE LIABLE FOR ANY
DIRECT, INCIDENTAL, OR CONSEQUENTIAL DAMAGES
OTHER THAN AS EXPRESSLY PROVIDED BY SPECIFIC
LAW. NO PERSON HAS THE AUTHORITY TO BIND
CORDIS TO ANY REPRESENTATION OR WARRANTY
EXCEPT AS SPECIFICALLY SET FORTH HEREIN.
Descriptions or specifications in Cordis printed matter,
including this publication, are meant solely to generally
describe the product at the time of manufacture and do
not constitute any express warranties.
Cordis Corporation will not be responsible for any direct,
incidental, or consequential damages resulting from
reuse of the product.
Protected under one or more of the following U.S. Patents:
5,843,244; 6,019,778; 6,129,755 and other U.S. and foreign
patents pending.

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