The Boston Scientific Coyote Balloon Catheter (REF H74939186350690) is a low-profile, over-the-wire percutaneous transluminal angioplasty (PTA) catheter engineered for navigating tortuous and small-vessel peripheral anatomy. Configured with a 3.5 mm balloon diameter and a 60 mm working length, the Coyote platform supports controlled dilatation in challenging access cases where deliverability and crossing profile are critical.
Key Features
Low-profile balloon design intended to facilitate crossing of tight or calcified lesions
Over-the-wire configuration compatible with 0.014 in guidewires (verify in current IFU)
Hydrophilic coating on the distal shaft to enhance trackability
Two radiopaque markers defining balloon working length under fluoroscopy
Semi-compliant balloon material for predictable inflation behavior
Engineered for use through low-French introducer sheaths to support minimally invasive access
Clinical Applications
Peripheral transluminal angioplasty of stenotic lesions in the peripheral vasculature
Treatment of small-vessel and below-the-knee anatomy where low crossing profile is required
Post-dilatation following stent deployment, when clinically indicated
Navigation of tortuous peripheral arterial segments
Refer to the manufacturer's current Instructions for Use (IFU) for indications, contraindications, warnings, and patient selection criteria.
Product Information
Brand: Boston Scientific
Product Family: Coyote Balloon Catheter
Category: Peripheral Balloon Catheters (PTA)
Balloon Diameter: 3.5 mm
Balloon Length: 60 mm
Catheter Type: Over-the-wire PTA balloon catheter
Guidewire Compatibility: 0.014 in (confirm with current IFU)
Working Length: Not specified in the located sources
Rated Burst Pressure: Not specified in the located sources
Nominal Pressure: Not specified in the located sources
Sheath Compatibility: Not specified in the located sources
REF/UPN: H74939186350690
Sterility: Supplied sterile; single-use device
Storage: Store per manufacturer labeling
Specifications are provided for procurement reference only; always verify against the current Boston Scientific product labeling and IFU prior to clinical use.