Embarc™ Microcatheter - Navilyst medical

Embarc MicrocatheterExperience the new standard.

Embarc MicrocatheterMultiple-Layer Braided Construction• Engineered tapered transition offers proximaladvancement with distal fl exibility forsuperselective access in tortuous anatomy• Platinum Iridium and stainless steel braided shaftfor enhanced visibility, kink resistance and optimalcatheter stability in embolic delivery and powerinjection• Extruded PTFE liner for smoothguidewire and embolic interface• 1000 psi injection pressureGLYCE Hydrophilic Coating• Ultra-durable hydrophilic coated outersurface increases trackability andenhances vessel navigationStrain Relief and OvermoldedClear Hub• Inner coiled strain relief for improvedkink resistance• Unique hub design with contouredwing for precise catheter controlAtraumatic Distal Tip• Formed distal tip designedfor improved trackability andvessel selectionRadiopaque Lumenand RO Marker• Platinum Iridium provideshigh visibility under fl uoroscopy• Swaged RO marker for dimensionalcontrol and navigation• Hub facilitates smooth delivery andconfi rmation of embolic material andchemotherapeutic agentsOrdering Information(Consult your local representative for product availability outside the United States.)UPN Proximal OD Distal OD Distal ID Working Length TypeH965452040 3.0 F 2.4 F 0.021 in 105 cm StandardH965452100 3.0 F 2.4 F 0.021 in 135 cm StandardH965452160 3.0 F 2.4 F 0.021 in 150 cm StandardH965452220 3.0 F 2.8 F 0.027 in 105 cm High FlowH965452280 3.0 F 2.8 F 0.027 in 135 cm High FlowH965452340 3.0 F 2.8 F 0.027 in 150 cm High FlowEmbarc, Glyce and Navilyst Medical are trademarks and/or registered trademarks of Navilyst Medical, Inc.EMBARC MICROCATHETERINTENDED USE/INDICATIONS FOR USE: The Embarc Microcatheter with Glyce Hydrophilic Coating is intended for use in small vessels and superselective anatomyduring diagnostic and interventional procedures in the peripheral vasculature. Upon access of the desired region, the microcatheter can be used for the controlled andselective infusion of diagnostic, therapeutic and embolic materials. All products delivered through the microcatheter must be used in accordance with the originalmanufacturer’s instructions for use. The catheter is not intended for use in coronary or neuro vasculature.CONTRAINDICATIONS: None known.WARNINGS: Do not exceed the dynamic infusion pressure listed. Infusion pressure in excess of the indicated maximum may result in catheter rupture and patientinjury. The maximum dynamic infusion pressure for the Embarc Microcatheter with Glyce Hydrophilic Coating O.D: 2.8 F (0.93 mm) - 1000 psi (6895 kPa) and 2.4 F(0.81 mm) - 1000 psi (6895 kPa). Static pressure should not exceed 300 psi (2068 kPa). Exceeding indicated pressure may result in microcatheter rupture andpatient injury.PRECAUTIONS: The Glyce Hydrophilic Coating must be kept hydrated in order to be lubricious. This can be accomplished by attaching the rotating hemostatic valve toa continuous saline drip. Excessive tightening of the rotating hemostatic valve may result in damage to the microcatheter. The guidewire insertion tool, torque deviceand shaping mandrel are not intended to enter the body. This product is intended for use by physicians trained and experienced in small vessel access andinterventional procedures. Standard techniques for placement of percutaneous catheters should be employed.Refer to Directions for Use provided with the product for complete instructions, warnings and precautions.CAUTION: Federal Law (USA) restricts this device to sale by or on the order of a physician.Navilyst Medical, Inc.26 Forest StreetMarlborough, MA 01752www.navilystmedical.comFor more information, call800.833.9973 in the United States800.268.0184 in Canada© 2012 Navilyst Medical, Inc., or its affi liates.All rights reserved.NAVPS250NA (Rev. 1) / 02/12