1708000
Bard PowerPort Ti Implantable Port 8F, Silicone-Filled, Attachable Polyurethane, Intermediate
$211.00
eaches
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Description
PowerPort Implantable Port
1708000
- Single Lumen, Titanium, Full Size Profile
- Intermediate Kit
- Attachable Radiopaque Polyurethane Open-Ended Single-Lumen Venous Catheter 8F x 45cm
- PowerPort Titanium Implantable Port, Max Power Injection Flow Rate (5 mL/s with 19G PowerLoc Safety Infusion Set)
- Non-Coring Needle, 22G x 25mm, Straight
- Non-Coring Needle, 22G x 25mm, Right Angle
- Syringe, 12ml
- Introducer Needle, 18G x 70mm
- PowerLoc Safety Infusion Set, 20G x 25mm
- Tunneler
- Vein Pick
- Catheter Lock
- Guidewire, J-Tip (3mm Radius) with Straightener, 0.035" x 45cm
- AirGuard Valved Introducer, Peel-Apart Sheath, 8F x 15cm with Vessel Dilator (1.0mm ID)
Additional information
| Size | 8.0F |
|---|---|
| Arms | N/A |
| Manufacturer | |
| Unit | eaches |
- FDA Product Code: LJT
- FDA Product Code Name: PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR
- GMDN Term Code: 61494
- GMDN Term Name: Vascular port/catheter
- GMDN Term Description: A fully-implantable device assembly intended to provide access to arteries/veins (excludes coronary and intracerebral circulation) for infusion (e.g., chemotherapeutic agents, blood transfusions) and/or drainage (e.g., blood). It consists of: 1) a subcutaneous chamber, with a self-sealing puncturable septum for percutaneous insertion of a hypodermic needle; and 2) an attached catheter which passes into the arteries/veins. It may consist of two chambers attached to a dual-lumen catheter for simultaneous infusion. It is made of metal [e.g., titanium (Ti)] and/or synthetic polymers (e.g., silicone); disposable devices associated with implantation may be included.
