Manufacturer > Boston Scientific > Devices > FilterWire EZ™ Embolic Protection System for Carotid Arteries

FilterWire EZ™ Embolic Protection System for Carotid Arteries

Device-Type

Embolic Protection

Manufacturer

Boston Scientific


With its advanced technology designed for simplicity and effectiveness, the FilterWire EZ Embolic Protection System is designed to deliver efficient, predictable protection.




Features and Benefits

 

FilterWire EZ schematic

 

To view product information for the FilterWire EZ Embolic Protection System specific to use in SVGs, click here.


Product Information


Captures Debris Efficiently:

  • Uniform 110-micron-pore filter is designed to permit continuous blood flow while maintaining embolic capture efficiency.
  • Suspended nitinol filter loop is intended to provide 360° apposition in straight or tortuous anatomy.
  • Radiopaque loop allows full deployment verification with one angiographic view.

Enhanced Ease of Use for Delivery and Retrieval:

  • Pre-loaded rapid exchange protection wire with peel-away delivery sheath is intended to simplify device preparation.
  • Highly flexible system is designed to provide excellent tracking through tortuous anatomy.
  • 3.2F crossing profile, tapered nosecone and silicone-coated tip are designed to facilitate lesion crossing.
  • Retrieval sheath is designed to maximize filter coverage while withdrawing through deployed stent.

Simplifies Filter Sizing:

  • One size is intended to provide protection in vessels with 3.5mm to 5.5mm diameter landing zone.

FilterWire EZ System nitinol filter loop

The FilterWire EZ System has a confirming, nitinol filter loop.

Safety informations

INTENDED USE/INDICATIONS FOR USE

The Boston Scientific FilterWire EZ™ Embolic Protection System is indicated for use as a guidewire and embolic protection system to contain and remove embolic material (thrombus/debris) while performing angioplasty and stenting procedures in coronary saphenous vein bypass grafts and carotid arteries. The diameter of the vessel at the site of filter loop placement should be between 2.25 mm and 5.5 mm for coronary saphenous vein bypass graft procedures and between 3.5 mm and 5.5 mm for carotid procedures.

The safety and effectiveness of this device as an embolic protection system have not been established in the cerebral vasculature, peripheral vessels other than carotid arteries, or in treating native coronaries, including acute myocardial infarction.


CONTRAINDICATIONS

  • Patients with severe allergy to heparin
  • Patients with bleeding diathesis or other disorders that limit the use of anticoagulant therapy


WARNINGS

  • Only physicians thoroughly trained in percutaneous intravascular techniques and procedures should use the FilterWire EZ Embolic Protection System (refer to Physician Training section).
  • The safety and effectiveness of coronary drug-eluting stents (DES) when used with embolic protection devices have not been established.
  • The safety and effectiveness of the FilterWire EZ Embolic Protection System have not been demonstrated with carotid stents other than the Carotid WALLSTENT® Monorail® Endoprosthesis and Delivery System (Carotid WALLSTENT Endoprosthesis) and the NexStent® Carotid Stent and Monorail Delivery System (NexStent Carotid Stent).
  • The appropriate antiplatelet and anticoagulation therapy should be administered pre- and post-procedure to minimize the risk of embolism and thrombosis.
  • Filter safety and effectiveness has not been tested with power injection.
  • Failure to follow recommended device preparation and delivery instructions may result in air embolism or other adverse reaction.

Potential adverse events

Possible adverse events associated with FilterWire EZ Embolic Protection System use and application procedure include, but are not limited to, the following:

  • Angina
  • Bleeding complications
  • Bradycardia or arrhythmias, including ventricular fibrillation or tachycardia
  • Congestive heart failure
  • Damage to or dislocation of the implanted stent(s)
  • Death
  • Detachment and/or implantation of a component of the system
  • Drug reaction, allergic reaction to contrast media, medications or device materials
  • Embolization of air, tissue, thrombus or other embolic debris
  • Emergent surgery
  • End organ ischemia/infarction
  • Headache
  • Hypotension/hypertension
  • Infection (local or systemic)
  • Myocardial infarction
  • No-reflow resulting from reduced blood flow through the FilterWire EZ System filter
  • Pain
  • Puncture site complications (i.e., vessel occlusion, hemorrhage, hematoma, pseudoaneurysm or arteriovenous fistula)
  • Renal insufficiency, kidney failure, hematuria
  • Stroke/cerebrovascular accident (CVA), transient ischemic attack (TIA) or seizure
  • Vessel damage, dissection, occlusion, aneurysm, perforation, rupture, injury, thrombosis, or spasm

Device Documents

Related Device SKUs

* Select 2 or more (upto 4) SKUs to compare.
SKU Name Device SKUs Model Crossing Profile Reference Vessel Diameter
EZ Bent Tip Retrieval Sheath
H749 50100-150 0 4.0F (1.3mm, 0.052") -
FilterWire EZ System, 190cm
H749 20100-190 0 3.2F (1.1mm, 0.042") 3.5mm-5.5mm
FilterWire EZ System, 300cm
H749 20100-300 0 3.2F (1.1mm, 0.042") 3.5mm-5.5mm
  • Model : H749 50100-150 0
  • Procedure : -
  • Crossing Profile : 4.0F (1.3mm, 0.052")
  • Model : H749 20100-190 0
  • Procedure : -
  • Crossing Profile : 3.2F (1.1mm, 0.042")
  • Reference Vessel Diameter : 3.5mm-5.5mm
  • Model : H749 20100-300 0
  • Procedure : -
  • Crossing Profile : 3.2F (1.1mm, 0.042")
  • Reference Vessel Diameter : 3.5mm-5.5mm

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