Coils

Coil Pusher-16

by Boston Scientific Corporation

A long, thin, manual surgical device intended to advance an embolization implant (e.g. an embolic coil) through the length of an appropriate catheter so that the implant is ready for discharge (implantation) when the catheter has been surgically positioned at the target site in an artery or vein. The inserter, also known as a pusher, is removed prior to discharge of the implant. This is a single-use device.

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Where to buy Coil Pusher-16

Contact Boston Scientific Corporation directly; they can quote, ship, or point you to the distributor for your country.

From bostonscientific.com, checked October 2026.

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Procedures that use coils

Frequently asked questions

What is Coil Pusher-16 used for?

A long, thin, manual surgical device intended to advance an embolization implant (e.g. an embolic coil) through the length of an appropriate catheter so that the implant is ready for discharge (implantation) when the catheter has been surgically positioned at the target site in an artery or vein. The inserter, also known as a pusher, is removed prior to discharge of the implant. This is a single-use device.

Who makes Coil Pusher-16?

Coil Pusher-16 is made by Boston Scientific Corporation. It is listed under embolization coils in our device library.

What sizes does Coil Pusher-16 come in?

The FDA device database does not list sizes for Coil Pusher-16. Check the instructions for use or ask a Boston Scientific Corporation representative.

Is Coil Pusher-16 MRI safe?

The FDA device database entry for Coil Pusher-16 does not state its MRI safety status. Check the labeling before MRI.

Is Coil Pusher-16 FDA cleared?

Coil Pusher-16 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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