Angioplasty balloons
Coyote ES
by Boston Scientific Corporation
A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device.
Contact Boston Scientific Corporation ↗ Where to buy Compare similar devices
Find similar PTA balloons
Where to buy Coyote ES
Contact Boston Scientific Corporation directly; they can quote, ship, or point you to the distributor for your country.
From bostonscientific.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
Coyote ES 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 |
|---|---|---|---|
| H74939134152010 | — | Not stated | Available |
| H74939134202010 | — | Not stated | Available |
| H74939134203010 | — | Not stated | Available |
| H74939134204010 | — | Not stated | Available |
| H74939134252010 | — | Not stated | Available |
| H74939134253010 | — | Not stated | Available |
| H74939134254010 | — | Not stated | Available |
| H74939134302010 | — | Not stated | Available |
| H74939134303010 | — | Not stated | Available |
| H74939134304010 | — | Not stated | Available |
| H74939134352010 | — | Not stated | Available |
| H74939134353010 | — | Not stated | Available |
| H74939134354010 | — | Not stated | Available |
| H74939134402010 | — | Not stated | Available |
| H74939134403010 | — | Not stated | Available |
| H74939134404010 | — | Not stated | Available |
| H74939135152010 | — | Not stated | Available |
| H74939135202010 | — | Not stated | Available |
| H74939135203010 | — | Not stated | Available |
| H74939135204010 | — | Not stated | Available |
| H74939135252010 | — | Not stated | Available |
| H74939135253010 | — | Not stated | Available |
| H74939135254010 | — | Not stated | Available |
| H74939135302010 | — | Not stated | Available |
| H74939135303010 | — | Not stated | Available |
| H74939135304010 | — | Not stated | Available |
| H74939135352010 | — | Not stated | Available |
| H74939135353010 | — | Not stated | Available |
| H74939135354010 | — | Not stated | Available |
| H74939135402010 | — | Not stated | Available |
| H74939135403010 | — | Not stated | Available |
| H74939135404010 | — | Not stated | Available |
Procedures that use angioplasty balloons
Frequently asked questions
What is Coyote ES used for?
A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device.
Who makes Coyote ES?
Coyote ES is made by Boston Scientific Corporation. It is listed under peripheral angioplasty balloons in our device library.
What sizes does Coyote ES come in?
The FDA device database does not list sizes for Coyote ES. Check the instructions for use or ask a Boston Scientific Corporation representative.
Is Coyote ES MRI safe?
The FDA device database entry for Coyote ES does not state its MRI safety status. Check the labeling before MRI.
Is Coyote ES FDA cleared?
Coyote ES 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.