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.

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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.SizeMRIStatus
H74938046102070β€” MR ConditionalAvailable
H74938046104070β€” MR ConditionalAvailable
H74938046106070β€” MR ConditionalAvailable
H74938046620750β€” MR ConditionalAvailable
H74938046630750β€” MR ConditionalAvailable
H74938046640750β€” MR ConditionalAvailable
H74938046660750β€” MR ConditionalAvailable
H74938046720750β€” MR ConditionalAvailable
H74938046730750β€” MR ConditionalAvailable
H74938046740750β€” MR ConditionalAvailable
H74938046760750β€” MR ConditionalAvailable
H74938046820750β€” MR ConditionalAvailable
H74938046830750β€” MR ConditionalAvailable
H74938046840750β€” MR ConditionalAvailable
H74938046860750β€” MR ConditionalAvailable
H74938046920750β€” MR ConditionalAvailable
H74938046940750β€” MR ConditionalAvailable
H74938046960750β€” MR ConditionalAvailable
H74938047120130β€” MR ConditionalAvailable
H74938047140130β€” MR ConditionalAvailable
H74938047160130β€” MR ConditionalAvailable
H74938047620130β€” MR ConditionalAvailable
H74938047630130β€” MR ConditionalAvailable
H74938047640130β€” MR ConditionalAvailable
H74938047660130β€” MR ConditionalAvailable
H74938047720130β€” MR ConditionalAvailable
H74938047730130β€” MR ConditionalAvailable
H74938047740130β€” MR ConditionalAvailable
H74938047760130β€” MR ConditionalAvailable
H74938047820130β€” MR ConditionalAvailable
H74938047830130β€” MR ConditionalAvailable
H74938047840130β€” MR ConditionalAvailable
H74938047860130β€” MR ConditionalAvailable
H74938047920130β€” MR ConditionalAvailable
H74938047940130β€” MR ConditionalAvailable
H74938047960130β€” MR ConditionalAvailable

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.

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