Peripheral stents

Zilver Flex

by Cook Ireland Ltd

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.

Contact a rep Compare similar devices

Zilver Flex models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
G03796β€” MR ConditionalAvailable
G03797β€” MR ConditionalAvailable
G03799β€” MR ConditionalAvailable
G03800β€” MR ConditionalAvailable
G03801β€” MR ConditionalAvailable
G03802β€” MR ConditionalAvailable
G18237β€” MR ConditionalAvailable
G18238β€” MR ConditionalAvailable
G18239β€” MR ConditionalAvailable
G18241β€” MR ConditionalAvailable
G18243β€” MR ConditionalAvailable
G18244β€” MR ConditionalAvailable
G18245β€” MR ConditionalAvailable
G18246β€” MR ConditionalAvailable
G18247β€” MR ConditionalAvailable
G18249β€” MR ConditionalAvailable
G18250β€” MR ConditionalAvailable
G18251β€” MR ConditionalAvailable
G18253β€” MR ConditionalAvailable
G18254β€” MR ConditionalAvailable
G18255β€” MR ConditionalAvailable
G18258β€” MR ConditionalAvailable
G18260β€” MR ConditionalAvailable
G18262β€” MR ConditionalAvailable
G18264β€” MR ConditionalAvailable
G18265β€” MR ConditionalAvailable
G18266β€” MR ConditionalAvailable
G18268β€” MR ConditionalAvailable
G18271β€” MR ConditionalAvailable
G18272β€” MR ConditionalAvailable
G18274β€” MR ConditionalAvailable
G18275β€” MR ConditionalAvailable
G18277β€” MR ConditionalAvailable
G18278β€” MR ConditionalAvailable
G18281β€” MR ConditionalAvailable
G18282β€” MR ConditionalAvailable
G18284β€” MR ConditionalAvailable
G18287β€” MR ConditionalAvailable
G18288β€” MR ConditionalAvailable
G18293β€” MR ConditionalAvailable
G18296β€” MR ConditionalAvailable
G18297β€” MR ConditionalAvailable
G18301β€” MR ConditionalAvailable
G18302β€” MR ConditionalAvailable
G18303β€” MR ConditionalAvailable
G18304β€” MR ConditionalAvailable
G18306β€” MR ConditionalAvailable
G18307β€” MR ConditionalAvailable
G18310β€” MR ConditionalAvailable
G18311β€” MR ConditionalAvailable
G18312β€” MR ConditionalAvailable
G18313β€” MR ConditionalAvailable
G18314β€” MR ConditionalAvailable
G18315β€” MR ConditionalAvailable
G18316β€” MR ConditionalAvailable
G18317β€” MR ConditionalAvailable
G18318β€” MR ConditionalAvailable
G18319β€” MR ConditionalAvailable
G18320β€” MR ConditionalAvailable
G18321β€” MR ConditionalAvailable
G23751β€” MR ConditionalAvailable
G23752β€” MR ConditionalAvailable
G23753β€” MR ConditionalAvailable
G23754β€” MR ConditionalAvailable
G23755β€” MR ConditionalAvailable
G23756β€” MR ConditionalAvailable
G23757β€” MR ConditionalAvailable
G23758β€” MR ConditionalAvailable
G23759β€” MR ConditionalAvailable
G23760β€” MR ConditionalAvailable
G23761β€” MR ConditionalAvailable
G23762β€” MR ConditionalAvailable
G61167β€” MR ConditionalAvailable
G61168β€” MR ConditionalAvailable
G61169β€” MR ConditionalAvailable
G61170β€” MR ConditionalAvailable
G61171β€” MR ConditionalAvailable
G61172β€” MR ConditionalAvailable
G61173β€” MR ConditionalAvailable
G61174β€” MR ConditionalAvailable
G61175β€” MR ConditionalAvailable
G61176β€” MR ConditionalAvailable
G61177β€” MR ConditionalAvailable
G61178β€” MR ConditionalAvailable
G61179β€” MR ConditionalAvailable
G61180β€” MR ConditionalAvailable
G61181β€” MR ConditionalAvailable
G61182β€” MR ConditionalAvailable
G61183β€” MR ConditionalAvailable
G61184β€” MR ConditionalAvailable
G61185β€” MR ConditionalAvailable
G61186β€” MR ConditionalAvailable
G61187β€” MR ConditionalAvailable
G61188β€” MR ConditionalAvailable
G61189β€” MR ConditionalAvailable
G61190β€” MR ConditionalAvailable
G61191β€” MR ConditionalAvailable
G61192β€” MR ConditionalAvailable
G61193β€” MR ConditionalAvailable
G61194β€” MR ConditionalAvailable
G61195β€” MR ConditionalAvailable
G61196β€” MR ConditionalAvailable
G61197β€” MR ConditionalAvailable
G61198β€” MR ConditionalAvailable

Procedures that use peripheral stents

Frequently asked questions

What is Zilver Flex 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 Zilver Flex?

Zilver Flex is made by Cook Ireland Ltd. It is listed under peripheral artery stents and covered stents in our device library.

What sizes does Zilver Flex come in?

The FDA device database does not list sizes for Zilver Flex. Check the instructions for use or ask a Cook Ireland Ltd representative.

Is Zilver Flex MRI safe?

The FDA device database lists Zilver Flex as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is Zilver Flex FDA cleared?

Zilver Flex is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Cook Ireland Ltd sales representative?

Cook Ireland Ltd has not listed representatives on LA Vascular yet. Visit the Cook Ireland Ltd 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.

πŸ“¬ The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you