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SpiderFX® Embolic Protection Device

Filter the Risk

The SpiderFX® Embolic Protection Device allows the use of any 0.014" - 0.018" guidewire for initial lesion cross and SpiderFX delivery catheter placement. The SpiderFX filter is deployed and recovered through a dual-ended and low-profile catheter compatible with a guide catheter/sheath minimum ID of 0.066" (typically a 6F guide catheter or 5F access/long sheath). All components of the device are delivered in a single hoop, with Capture Wire/Nitinol braid Filter pre-loaded in the Delivery End of the SpiderFX Catheter.

Guidewire of Choice
  • The SpiderFX Device allows atraumatic lesion crossing with YOUR CHOICE of any 0.014" or 0.018" guidewire

Superior trackability

6F guide/5F sheath compatible RX delivery catheter with low 3.2F crossing profile
  • New Flexible Hypotube Connector reduces maximum force required to push filter by an average of 40% compared to SpideRX®
  • 320 cm / 190 cm snapwire and 190 cm wire length options for OTW and RX device interventions

Enhanced Visibility
  • Clearly visible radiopaque markers enable fast filter positioning
  • New direct mouth indicator provides enhanced visualization of filter mouth opening

    FXangio

Excellent Stability

Controlled filter positioning throughout the intervention and during device exchanges:
  • Braided nitinol design provides full wall apposition
  • Capture Wire is designed to rotate and move longitudinally independent of the filter

    FXstability
Size and Indication

SpiderFX offers a broad size range of filter sizes (3 mm - 7 mm) — select the most appropriate filter for Carotid Interventions
SpiderFX - NEURO
Component CAPTURE WIRE DELIVERY END RECOVERY END GUIDE CATHETER / SEATH
Model Number Filter Size (mm) Lumen Size (mm) Wire Length OTW/RX (cm) Wire Diameter (inch/mm) Crossing Profile (F) Diameter (F) Minimun ID (inch)
SPD2-US-030-190 3 3.0 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-030-320 3 3.0 320/190 0.014/0.36 3.2 4.2 0.066
SPD2-US-040-190 4 3.1-4.0 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-040-320 4 3.1-4.0 320/190 0.014/0.36 3.2 4.2 0.066
SPD2-US-050-190 5 4.1-5.0 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-050-320 5 4.1-5.0 320/190 0.014/0.36 3.2 4.2 0.066
SPD2-US-060-190 6 4.5-6.0 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-060-320 6 4.5-6.0 320/190 0.014/0.36 3.2 4.2 0.066
SPD2-US-070-190 7 5.5-6.0 SVG / 5.5-7.0 Carotid 190 0.014/0.36 3.2 4.2 0.066
SPD2-US-070-320 7 5.5-6.0 SVG / 5.5-7.0 Carotid 320/190 0.014/0.36 3.2 4.2 0.066
Carotid Indication: The SpiderFX Embolic Protection Device 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 carotid arteries. The diameter of the artery at the site of the filter basket placement should be between 3.0 mm and 7.0 mm.
CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician. Indications, contraindications, warnings and instructions for use can be found in the product labeling supplied with each device.