SPD2-US-030-320
ev3 SpiderFX Embolic Protection Device: 3.0mm x 320/190cm x 0.014″
Original price was: $230.00.$57.50Current price is: $57.50.
box of 1
In Stock: 94 Eaches
Expiration:
Expired
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The item listed above is expired and may be used for educational, training, and non-clinical research purposes only. Any product information appearing below, including the product indication statement, pertains to an in-date item only.
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Description
Medtronic ev3 SpiderFX™ Embolic Protection Device
Embolic protection devices are used to capture and remove debris that becomes dislodged during an interventional procedure. Embolic debris may flow downstream and block smaller vessels, resulting in procedural complications or poor patient outcomes.
Debris Matters
Debris can occur with any endovascular procedure and may lead to complications or poor patient outcomes.
Choice Matters
The SpiderFX Embolic Protection Device can be delivered over any 0.014” or 0.018” guidewire or through any 0.035” catheter, allowing physicians to choose their method of delivery for successful placement even in challenging access situations.
Design Features
SpiderFX has a unique braided Nitinol filter that conforms to the vessel wall and maintains full-wall apposition during the intervention. Flow is directed into the filter’s conical design, effectively capturing debris while maintaining blood flow.
A gold Tungsten loop around the mouth of the filter and radiopaque markers allow for precise positioning and verification of apposition before proceeding with the intervention.
The capture wire (available in 190cm and 320cm) rotates and moves longitudinally independent of the filter for enhanced stability during the procedure.
Additional information
| Size | 3.00mm |
|---|---|
| Arms | N/A |
| Manufacturer | |
| Unit | box of 1 |
- FDA Product Code: NTE
- FDA Product Code Name: Temporary Carotid Catheter For Embolic Capture
- GMDN Term Code: 44841
- GMDN Term Name: Embolic protection filtering guidewire
- GMDN Term Description: A steerable wire with a filter at its distal end intended to be used to facilitate the placement of diagnostic/interventional vascular devices (e.g., angioplasty balloons, intravascular stents) in the lumen of a blood vessel (coronary, carotid, peripheral), and to provide embolic protection by capturing emboli that may result from the procedure. The filter is deployable (expandable) once inserted distal to the vascular lesion (e.g., atherosclerotic plaque). It typically includes devices for introduction/removal of the guidewire (e.g., deployment/removal sheath), which are not intended to be used as working channels for other interventional devices. This is a single-use device.
