
7
DISClAIMER OF WARRANTY
BARD PERIPHERAl VASCUlAR, INC. WARRANTS TO THE FIRST PURCHASER OF THIS PRODUCT, THAT THIS PRODUCT
WIll BE FREE FROM DEFECTS IN MATERIAlS AND WORKMANSHIP FOR A PERIOD OF ONE YEAR FROM THE DATE OF FIRST
PURCHASE AND lIABIlITY UNDER THIS lIMITED PRODUCT WARRANTY WIll BE lIMITED, TO REPAIR OR REPlACEMENT
OF THE DEFECTIVE PRODUCT, IN BARD‘S SOlE DISCRETION, OR REFUNDING YOUR NET PRICE PAID. WEAR AND TEAR
FROM NORMAl USE OR DEFECTS RESUlTING FROM MISUSE OF THIS PRODUCT IS NOT COVERED BY THIS lIMITED
WARRANTY.
TO THE EXTENT AllOWABlE BY APPlICABlE lAW, THIS lIMITED PRODUCT WARRANTY IS IN lIEU OF All OTHER
WARRANTIES, WHETHER EXPRESS OR IMPlIED, INClUDING, BUT NOT lIMITED TO, ANY IMPlIED WARRANTY OF
MERCHANTABIlITY OR FITNESS FOR A PARTICUlAR PURPOSE. IN NO EVENT WIll BARD PERIPHERAl VASCUlAR, INC.
BE lIABlE TO YOU FOR ANY INDIRECT, INCIDENTAl OR CONSEQUENTIAl DAMAGES RESUlTING FROM YOUR HANDlING
OR USE OF THIS PRODUCT.
Some countries do not allow an exclusion of implied warranties, incidental or consequential damages. You may be entitled to
additional remedies under the laws of your country.
• With the distal end of the stent apposing the vessel wall, final deployment can be continued, depending on user
preference, with rotating the small (labeled 3 on the system grip) or the large thumbwheel (Figure 12).
Figure 12:
Overview of large and small thumbwheels
• Deployment of the stent is complete when the proximal stent radiopaque markers appose the vessel wall.
DO NOT
attempt to recapture the stent.
F. Post Stent Placement
• Remove the delivery system from the body.
Note:
If resistance is met while retracting the delivery system over a guidewire, remove the delivery system and
guidewire together.
• Post stent expansion with a balloon dilatation catheter is recommended. If performed, select a balloon catheter that
matches the size of the reference vessel, but that is not larger than the stent diameter itself.
• Remove the guidewire and introducer sheath from the body.
• Close entry wound as appropriate.
• Discard the delivery system, guidewire and introducer sheath following institutional procedures.
Note:
Physician experience and discretion will determine the appropriate antithrombotic drug regimen for each
individual patient.
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