Go the Distance Without CompromiseRAPIDTRANSIT® Microcatheter

M I C R O C AT H E T E R S

• Small Profile (2.3F) / Large Inner Diameter (0.021 in.)

• Proximal Stainless Steel Braid Providing Controlled Pushability and Kink Resistance

• Distal Platinum Coil for Flexibility and Lumen Integrity

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Usable Distal Flexible Tip

Catalog No. Length (cm) Length (cm) Markers

601-210 70 30 1601-251 150 50 1601-251X 150 50 2601-271 170 50 1

RAPIDTRANSIT® Microcatheters

ordering information:

Designed for fast and smooth accessthrough tortuous vasculature

•ProprietaryBraid/CoilConstruction•OuterDiameter(proximal):2.8F•OuterDiameter(distal):2.3F• InnerDiameter:0.021in.•Guidewire:≤0.018in.•GuidingCatheter:

Minimum0.042in.ID (shouldaccept0.038in.guidewire)•OuterCoating:Hydrophilic• InnerCoating: PTFELiner

SpecificationS compatibility

•CompatiblewiththeTRUFILL® DCS ORBIT®DetachableCoilSystem

•PVA:1,000micronsmax.

Clear,NylonHub Strain Relief 2.8FProx.OD

Coiled Distal Section Radiopaque Marker

2.3FDistalOD

DistalFlexibleLength(cm)30/50

60cm/150cm/170cm

0.021”ID

BraidedBody

RAPIDTRANSIT® Essential Prescribing Information (EPI)Caution: Federal (USA) law restricts this product to sale by or on the order of a physician. INDICATIONS: The Codman Neurovascular Infusion Catheters are intended to be used as a mechanism for the infusion of various diagnostic, embolic, and therapeutic agents into the vascular systems and for superselective angiography of the peripheral and coronary vasculatures. All agents must be used in accordance with manufacturer’s “Instructions for Use.” It is recommended that the Codman Neurovascular Infusion Catheters be used with a guiding catheter, a compatible catheter sheath introducer and a steerable guidewire. CONTRAINDICATIONS: None known. WARNINGS: THIS DEVICE IS INTENDED FOR ONE USE ONLY. Discard the infusion catheter after one procedure. Structural integrity and/or function may be impaired through reuse or cleaning. Catheters are extremely difficult to clean after exposure to biological materials and may cause adverse patient reactions if reused. Never advance or withdraw an intraluminal device against resistance until the cause of resistance is determined by fluoroscopy. If the cause cannot be determined, withdraw the catheter. Movement against resistance may result in damage to the vessel. The infusion pressure should not exceed the maximum listed pressure for each catheter, as indicated in the flowrate charts. Pressure in excess of the recommended range may result in catheter rupture or tip severance. PRECAUTIONS: Store in a cool, dark, dry place. Do not use if package is open or damaged. Use prior to the “Use By” date. Read and follow the “Instructions for Use” of all agents or contrast media used with the infusion catheters. COMPLICATIONS: Procedures requiring percutaneous catheter introduction should not be attempted by physicians unfamiliar with the possible complications, which may occur during or after the procedure. Possible complications include, but are not limited to, the following: embolism; hematoma at the punctured site; infection; dissection; perforation of vessel wall; and/or distal embolization.Other Important Information: Prior to use, please read full “Instructions for Use” supplied with these devices for more detailed product and use information.

Codman Neurovascular is a business unit of Codman & Shurtleff, Inc.RAPIDTRANSIT®,TRUFILL®andORBIT®areregisteredtrademarksofCodman&Shurtleff,Inc.©2009Codman&Shurtleff,Inc.AllRightsReserved. VC/SECNV-13-000

USACodman & Shurtleff, Inc.325 Paramount DriveRaynham,MA02767 www.codman.com

Toplaceanorder,call1-800-255-2500.

Fortechnical/productquestions,call1-800-225-0460.

Forproductavailability,pleasecontactyourCodmanNeurovascularrepresentative.

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