The Boston Scientific Coyote Balloon Catheter (REF H74939134152010) is a low-profile, over-the-wire percutaneous transluminal angioplasty (PTA) balloon dilatation catheter featuring a 1.5 mm balloon diameter and a 20 mm balloon working length. Engineered for trackability and crossability, the Coyote platform is designed to support procedures in tortuous, small-vessel and distal peripheral anatomy where a low crossing profile and flexible shaft are advantageous.
Key Features
Balloon diameter: 1.5 mm
Balloon working length: 20 mm
Low-profile, semi-compliant balloon designed for predictable inflation
Over-the-wire (OTW) design compatible with 0.014" guidewires (confirm with current IFU)
Hydrophilic-coated distal shaft to support trackability through tortuous anatomy
Tapered, flexible distal tip intended to enhance crossability
Radiopaque markers to assist balloon placement under fluoroscopy
Sterile, single-use device
Clinical Applications
Intended for use by trained interventional clinicians during endovascular procedures involving the peripheral vasculature. Typical use cases referenced for the Coyote platform include dilatation of stenoses in small and distal peripheral arteries and post-dilatation in select peripheral interventions. Clinicians should consult the current Boston Scientific Instructions for Use (IFU) for the complete list of indications, contraindications, warnings and precautions applicable in their region.
Product Information
Brand: Boston Scientific
Product line: Coyote Balloon Catheter
Category: Peripheral Balloon Catheters
REF / UPN: H74939134152010
Balloon size: 1.5 mm x 20 mm
Catheter working length: Not specified in the located sources
Guidewire compatibility: Not specified in the located sources
Minimum sheath/guide compatibility: Not specified in the located sources
Rated burst pressure (RBP) and nominal pressure: Not specified in the located sources
Sterilization: Sterile, single-use (refer to IFU)
Packaging: Individually packaged unit (refer to manufacturer labeling)
Regulatory status and indications vary by country; verify local clearance and IFU before procurement.