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> > > SpideRX® Embolic Protection Device

SpideRX® Embolic Protection Device

General Information

Vendor		ev3, Inc.
Item		SpideRX® Embolic Protection Device
Features		Pre-Loaded Filter/Capture Wire - Ready to flush and deploy with no stylet or introducer needed Fully Rapid Exchange - For quick delivery and recovery 6 Fr Guide Catheter Compatible (minimum 0.066" I.D.) - To use with desired interventional devices Use of Separate Preferred 0.014" - 0.018" Guidewire - Reliable access and tight lesion crossing in straight and tortuous anatomy Single Dual-Ended Low-Profile Catheter - Fewer components to manage during procedure Low 3.2 Fr Crossing profile - Minimal interaction with the lesion during catheter placement Unique Nitinol Filter Design - Provides full body wall apposition, and the ability to capture debris Multiple Filter Sizes (3.0, 4.0, 5.0, 6.0, 7.0 mm) - Optimal matching of the filter to the vessel size Longitudinal/Rotational Wire Movement - Filter designed to remain stationary during the intervention and device exchanges Radiopaque Gold Proximal Marker - Visualization of filter apposition throughout intervention 4.2 Fr Recovery Catheter - Easily accommodates filter with debris Rapid Exchange Recovery Catheter - For easy recovery after intervention
Approval		Inquire
Product Number		Inquire
Shaft O.D. (inches)		Inquire
Total Length (cm)		Inquire
Pricing		Inquire

Product Description

The SpideRX® Embolic Protection Device features the ability to use a separate, preferred guidewire to cross the lesion and a pre-loaded nitinol filter with a dual-ended catheter for delivery and recovery. Offering a fully rapid exchange system, the SpideRX Device is easy to use in the indicated applications:

Carotid Indication - The SpideRX 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 filter basket placement should be between 3.0 mm and 7.0 mm.

SVG Indication - The SpideRX Embolic Protection Device is indicated for use as an embolic protection system to contain and remove embolic material (thrombus/debris). The device also acts as the guidewire while performing percutaneous transluminal coronary angioplasty or stenting procedures in coronary saphenous vein bypass grafts with reference vessel diameters of 3.0 to 6.0 mm. The safety and effectiveness of this device as an embolic protection system has not been established in the cerebral and peripheral vasculature.

NOTE: Medcompare disclaims any information on this site. The information found on Medcompare (Drug Guide, Product Listings and otherwise) is intended for use by medical professionals. This information is not intended to replace the information, advice or instructions from a medical doctor. Pricing information is approximate, actual prices may vary.