Vaxcel® Implantable Ports - Boston Scientific
Vaxcel® Implantable Ports - Boston Scientific
Vaxcel® Implantable Ports - Boston Scientific
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Vaxcel ® <strong>Implantable</strong> <strong>Ports</strong><br />
Ordering Information<br />
Vaxcel <strong>Implantable</strong> Port Kits<br />
Catheter Catheter Introducer<br />
Order Port Catheter O.D. I.D. Sheath<br />
UPN Number Material Material (F/mm) (mm) (F)<br />
Mini<br />
M001453030 45-303 Titanium Polyurethane 6/1.9 1.1 6<br />
M001453050 45-305 Titanium Polyurethane 7/2.2 1.3 7<br />
M001453100 45-310 Titanium Silicone 8/2.6 1.5 8<br />
Standard<br />
M001453400 45-340 Polysulfone Silicone 8/2.6 1.5 8<br />
M001453200 45-320 Titanium Silicone 8/2.6 1.5 8<br />
M001453600 45-360 Polysulfone Polyurethane 9/2.8 1.8 9<br />
M001453150 45-315 Titanium Polyurethane 9/2.8 1.8 9<br />
Each Kit Includes: Vaxcel <strong>Implantable</strong> Port with Attachable Thin Walled Catheter, 63cm Length; Twist-On Locking<br />
Collar Connector; 18 Gauge, 2.75" Introducer Needle; .038" “J” Guidewire with Tip Straightener;<br />
Peelable Introducer/Dilator Set; Tunneler; 0.5" Blunt Cannula; 12mL Slip Lock Syringe; 12mL Syringe;<br />
22 Gauge, 1" Straight Non-Coring Needle; 22 Gauge, 1" 90° Non-Coring Needle<br />
The <strong>Boston</strong> <strong>Scientific</strong> Commitment to Service…<br />
Technical support for this product and other <strong>Boston</strong> <strong>Scientific</strong> Venous Access Products<br />
is available 24 hours a day by calling the:<br />
Venous Access Products Reference Line: 1.800.513.6876<br />
INDICATIONS FOR USE<br />
The Vaxcel ® <strong>Implantable</strong> Port Systems are designed for long-term vascular access allowing for administration of IV fluids,<br />
blood products, medications, parenteral nutrition solutions and, in addition, for blood withdrawal.<br />
CONTRAINDICATIONS<br />
The device is contraindicated when: the presence of other device related infection, bacteremia, septicemia or peritonitis is known or<br />
suspected; severe chronic obstructive lung disease exists; past irradiation of prospective insertion site; previous episodes of venous<br />
thrombosis or vascular surgical procedures at the prospective placement site; local tissue factors will prevent proper device<br />
stabilization and/or access; anticipation or presence of other central venous intraluminal devices, including pacemakers, is expected;<br />
hypercoagulopathy condition exists, unless considerations are made to place the patient on anticoagulation therapy; presence or<br />
suspicion of allergic reaction to materials contained in this device is a potential risk; body size is insufficient to accommodate size<br />
of the portal or the catheter; demonstrated intolerance for an implanted device. Venous access to the upper torso may be<br />
contraindicated due to anatomical constraints, such as burns to the upper body, cervicothoracic trauma, planned radiation therapy<br />
to the mediastinum, bilateral neck dissection and infected median sternotomy incisions.<br />
CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.<br />
Refer to package insert provided with the product for complete Instructions for Use, Contraindications, Potential Adverse Effects, Warnings<br />
and Precautions prior to using this product.<br />
<strong>Boston</strong> <strong>Scientific</strong> Corporation<br />
Oncology<br />
100 <strong>Boston</strong> <strong>Scientific</strong> Way<br />
Marlborough, MA 01752-1234<br />
www.bostonscientific.com<br />
To order product or for more<br />
information, contact Customer<br />
Service at 1.800.225.3238<br />
© 2005 <strong>Boston</strong> <strong>Scientific</strong> Corporation<br />
or its affiliates. All rights reserved.<br />
ONCPS130 (Rev.1) / 5M / 09/05
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