TIPS devices
WALLSTENT Endoprosthesis
by Boston Scientific Corporation
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
WALLSTENT 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 |
|---|---|---|---|
| H965402110 | — | MR Conditional | Available |
| H965402120 | — | MR Conditional | Available |
| H965402130 | — | MR Conditional | Available |
Procedures that use tips devices
Frequently asked questions
What is WALLSTENT Endoprosthesis used for?
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
Who makes WALLSTENT Endoprosthesis?
WALLSTENT Endoprosthesis is made by Boston Scientific Corporation. It is listed under tips stent grafts and access sets in our device library.
What sizes does WALLSTENT Endoprosthesis come in?
The FDA device database does not list sizes for WALLSTENT Endoprosthesis. Check the instructions for use or ask a Boston Scientific Corporation representative.
Is WALLSTENT Endoprosthesis MRI safe?
The FDA device database lists WALLSTENT Endoprosthesis as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is WALLSTENT Endoprosthesis FDA cleared?
WALLSTENT Endoprosthesis is registered in the FDA's Global Unique Device Identification Database (GUDID).
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.