Peripheral stents
WALLSTENT RP Endoprosthesis
by Boston Scientific Corporation
A non-bioabsorbable tubular device intended to be implanted in the common and/or external iliac artery(ies) to maintain arterial patency and luminal diameter in patients with symptomatic atherosclerotic disease. It is made of metal [e.g., stainless steel, nickel-titanium alloy (Nitinol)] and may be inserted with a balloon catheter which causes the device to expand when inflated, or it may self-expand after insertion with a delivery device. It may be a continuous tube or a mesh structure in tubular form and is available in a variety of lengths and diameters. Disposable devices associated with implantation may be included.
WALLSTENT RP Endoprosthesis models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| M001711240 | — | MR Conditional | Available |
| M001711260 | — | MR Conditional | Available |
| M001711280 | — | MR Conditional | Available |
| M001711300 | — | MR Conditional | Available |
| M001711340 | — | MR Conditional | Available |
| M001711360 | — | MR Conditional | Available |
| M001711380 | — | MR Conditional | Available |
| M001712000 | — | MR Conditional | Available |
| M001712010 | — | MR Conditional | Available |
| M001712020 | — | MR Conditional | Available |
| M001712030 | — | MR Conditional | Available |
| M001712040 | — | MR Conditional | Available |
| M001712050 | — | MR Conditional | Available |
| M001712060 | — | MR Conditional | Available |
| M001712070 | — | MR Conditional | Available |
| M001712080 | — | MR Conditional | Available |
| M001712090 | — | MR Conditional | Available |
| M001712100 | — | MR Conditional | Available |
| M001712110 | — | MR Conditional | Available |
| M001712120 | — | MR Conditional | Available |
| M001712130 | — | MR Conditional | Available |
| M001712140 | — | MR Conditional | Available |
| M001712150 | — | MR Conditional | Available |
| M001712160 | — | MR Conditional | Available |
| M001712170 | — | MR Conditional | Available |
| M001712180 | — | MR Conditional | Available |
| M001712190 | — | MR Conditional | Available |
| M001712200 | — | MR Conditional | Available |
| M001712210 | — | MR Conditional | Available |
| M001712220 | — | MR Conditional | Available |
| M001712230 | — | MR Conditional | Available |
| M001712240 | — | MR Conditional | Available |
| M001712250 | — | MR Conditional | Available |
| M001712260 | — | MR Conditional | Available |
| M001712270 | — | MR Conditional | Available |
| M001712280 | — | MR Conditional | Available |
| M001712290 | — | MR Conditional | Available |
| M001712300 | — | MR Conditional | Available |
| M001712310 | — | MR Conditional | Available |
| M001712320 | — | MR Conditional | Available |
| M001712330 | — | MR Conditional | Available |
| M001712340 | — | MR Conditional | Available |
| M001712350 | — | MR Conditional | Available |
| M001712360 | — | MR Conditional | Available |
| M001712370 | — | MR Conditional | Available |
| M001712380 | — | MR Conditional | Available |
| M001712390 | — | MR Conditional | Available |
FDA clearances
- PMA P940019 October 2005
Procedures that use peripheral stents
Frequently asked questions
What is WALLSTENT RP Endoprosthesis used for?
A non-bioabsorbable tubular device intended to be implanted in the common and/or external iliac artery(ies) to maintain arterial patency and luminal diameter in patients with symptomatic atherosclerotic disease. It is made of metal [e.g., stainless steel, nickel-titanium alloy (Nitinol)] and may be inserted with a balloon catheter which causes the device to expand when inflated, or it may self-expand after insertion with a delivery device. It may be a continuous tube or a mesh structure in tubular form and is available in a variety of lengths and diameters. Disposable devices associated with implantation may be included.
Who makes WALLSTENT RP Endoprosthesis?
WALLSTENT RP Endoprosthesis is made by Boston Scientific Corporation. It is listed under peripheral artery stents and covered stents, biliary drainage catheters, tips stent grafts and access sets in our device library.
What sizes does WALLSTENT RP Endoprosthesis come in?
The FDA device database does not list sizes for WALLSTENT RP Endoprosthesis. Check the instructions for use or ask a Boston Scientific Corporation representative.
Is WALLSTENT RP Endoprosthesis MRI safe?
The FDA device database lists WALLSTENT RP Endoprosthesis as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is WALLSTENT RP Endoprosthesis FDA cleared?
WALLSTENT RP Endoprosthesis is covered by FDA submission P940019.
How do I contact a Boston Scientific Corporation sales representative?
Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.