Peripheral stents
Express LD Iliac / Biliary
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.
Express LD Iliac / Biliary 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 |
|---|---|---|---|
| H74938046102070 | β | MR Conditional | Available |
| H74938046104070 | β | MR Conditional | Available |
| H74938046106070 | β | MR Conditional | Available |
| H74938046620750 | β | MR Conditional | Available |
| H74938046630750 | β | MR Conditional | Available |
| H74938046640750 | β | MR Conditional | Available |
| H74938046660750 | β | MR Conditional | Available |
| H74938046720750 | β | MR Conditional | Available |
| H74938046730750 | β | MR Conditional | Available |
| H74938046740750 | β | MR Conditional | Available |
| H74938046760750 | β | MR Conditional | Available |
| H74938046820750 | β | MR Conditional | Available |
| H74938046830750 | β | MR Conditional | Available |
| H74938046840750 | β | MR Conditional | Available |
| H74938046860750 | β | MR Conditional | Available |
| H74938046920750 | β | MR Conditional | Available |
| H74938046940750 | β | MR Conditional | Available |
| H74938046960750 | β | MR Conditional | Available |
| H74938047120130 | β | MR Conditional | Available |
| H74938047140130 | β | MR Conditional | Available |
| H74938047160130 | β | MR Conditional | Available |
| H74938047620130 | β | MR Conditional | Available |
| H74938047630130 | β | MR Conditional | Available |
| H74938047640130 | β | MR Conditional | Available |
| H74938047660130 | β | MR Conditional | Available |
| H74938047720130 | β | MR Conditional | Available |
| H74938047730130 | β | MR Conditional | Available |
| H74938047740130 | β | MR Conditional | Available |
| H74938047760130 | β | MR Conditional | Available |
| H74938047820130 | β | MR Conditional | Available |
| H74938047830130 | β | MR Conditional | Available |
| H74938047840130 | β | MR Conditional | Available |
| H74938047860130 | β | MR Conditional | Available |
| H74938047920130 | β | MR Conditional | Available |
| H74938047940130 | β | MR Conditional | Available |
| H74938047960130 | β | MR Conditional | Available |
Procedures that use peripheral stents
Frequently asked questions
What is Express LD Iliac / Biliary 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 Express LD Iliac / Biliary?
Express LD Iliac / Biliary is made by Boston Scientific Corporation. It is listed under peripheral artery stents and covered stents in our device library.
What sizes does Express LD Iliac / Biliary come in?
The FDA device database does not list sizes for Express LD Iliac / Biliary. Check the instructions for use or ask a Boston Scientific Corporation representative.
Is Express LD Iliac / Biliary MRI safe?
The FDA device database lists Express LD Iliac / Biliary as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Express LD Iliac / Biliary FDA cleared?
Express LD Iliac / Biliary 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.