Solid Foundationfor Access Support

ENVOY® and ENVOY® XB Guiding Catheters

G U I D I N G C AT H E T E R

• Available in Standard and Extra-Backup Support

• Hybrid Braid Delivers Maximum Flow Rates While Maintaining Catheter Support and Flexibility

Straight

Multipurpose C

Multipurpose D

Modified

Simmons 2

Headhunter 1

Available in 6 Shapes

12657 CNV Bro Envoy Codman BG.indd 1 4/17/09 11:28:20 AM

ENVOY® Guiding Catheters

ENVOY® and ENVOY® XB Guiding Catheters provide treatment options for procedural versatility. Soft radiopaque tip enables less traumatic vessel placement.

ENVOY® and ENVOY® XB Essential Prescribing Information (EPI) INDICATION: The ENVOY® Guiding Catheter is intended for use in the peripheral, coronary, and neurovasculature for the intravascular introduction of interventional/diagnostic devices. CONTRAINDICATIONS: None known. WARNINGS: Discard the guiding 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. Do not use with Ethiodol or Lipiodol* contrast media, or other such contrast media which incorporates the components of these agents. PRECAUTIONS: Store in a cool, dark, dry place. Do not use open or damaged packages. Use prior to the “Use By” date. Exposure to temperatures above 54º C (130º F) may damage the catheter. Do not expose to organic solvents. Inspect the guiding catheter before use to verify that its size, shape, and condition are suitable for the specific procedure. If strong resistance is met during manipulation, discontinue the procedure and determine the cause for the resistance before proceeding. If the cause of the resistance cannot be determined, withdraw the catheter. Extreme care must be taken to avoid damage to the vasculature through which the catheter passes. The guiding catheter may occlude smaller vessels. Care must be taken to avoid complete blood flow blockage. Torquing the catheter excessively while kinked may cause damage which could result in possible separation along the catheter shaft. Should the guiding catheter shaft become severely kinked, withdraw the entire system (guiding catheter, guidewire, and catheter sheath introducer). Advancement, manipulation, and withdrawal of the guiding catheter should always be performed under flouroscopic guidance.COMPLICATIONS: Procedures requiring percutaneous catheter introduction should not be attempted by physicians unfamiliar with the possible complications. Complications may occur at any time during or after the procedure. Possible complications include, but are not limited to the following: air embolism; hematoma at the puncture site; infection; and/or perforation of the heart or vessel wall. * Ethiodol and Lipiodol are trademarks of Guerbet S.A.Caution: Federal (USA) law restricts this product to sale by or on the order of a physician. Prior to use, please read full “Instructions for Use” supplied with these devices for more detailed product and use information.

ordering information:

ConStrUCtion

•LubriciousPTFEinnerlinerprovides smooth device passage

•Nylon/polyurethaneandstainlesssteel braidshaftmaterials

ComPatiBiLitY with mULtiPLe in-dweLLing deviCeS

Codman Neurovascular is a business unit of Codman & Shurtleff, Inc.ENVOY®,PROWLER®,andPROWLER®SELECT® are registered trademarks of Codman & Shurtleff, Inc.©2009Codman&Shurtleff,Inc.AllRightsReserved. VC/SECNV-07-000

USACodman & Shurtleff, Inc.325ParamountDriveRaynham,MA02767 www.codman.com

Toplaceanorder,call1-800-255-2500.

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

Forproductavailability,pleasecontactyourCodman Neurovascular representative.

Usable Catalog No. Length (cm) Shape

ENVOY® 5F - 0.056 in. ID (1.4mm)

556-26090 90 Straight 556-26000 100 Straight 556-25690 90 MultipurposeC 556-25600 100 MultipurposeC 556-25890 90 MultipurposeD556-25800 100 MultipurposeD 556-25090 90 ModifiedCerebral(Burke) 556-25000 100 ModifiedCerebral(Burke) 556-25490 90 Headhunter1 556-25400 100 Headhunter1

Usable Catalog No. Length (cm) Shape

ENVOY® 6F - 0.070 in. ID (1.8mm)

670-26090 90 Straight 670-26000 100 Straight 670-25690 90 MultipurposeC 670-25600 100 MultipurposeC 670-25890 90 MultipurposeD 670-25800 100 MultipurposeD 670-25090 90 ModifiedCerebral(Burke) 670-25000 100 ModifiedCerebral(Burke) 670-25490 90 Headhunter1 670-25400 100 Headhunter1 670-25290 90 Simmons2 670-25200 100 Simmons2

Usable Catalog No. Length (cm) Shape

ENVOY® XB 6F - 0.070 in. ID (1.8mm)

670-26090B 90 Straight 670-26000B 100 Straight 670-25690B 90 MultipurposeC 670-25600B 100 MultipurposeC 670-25890B 90 MultipurposeD 670-25800B 100 MultipurposeD 670-25090B 90 ModifiedCerebral(Burke) 670-25000B 100 ModifiedCerebral(Burke) 670-25490B 90 Headhunter1 670-25400B 100 Headhunter1 670-25290B 90 Simmons2 670-25200B 100 Simmons 2

The6FENVOY®or6FENVOY® XBiscompatiblewithaPROWLER® SELECT®PLuS or PROWLER®PLuS microcatheter and an additional devicewithamaximumouterdiameterof2.4Forless.

• Microcatheter 2.3F (.030”) PROWLER® SELECT® LPES PROWLER® 14 PROWLER® 10

• Additional Device with a maximum outer diameter of 2.9F (.038”) or less

• Microcatheter 2.8F (.037”) PROWLER® SELECT® Plus PROWLER® Plus

• Additional Device with a maximum outer diameter of 2.4F (.031”) or less

ENVOY® ID = .070”ENVOY® ID = .070”

Addl

Dev

ice

2.9F

(.0

38”)

or

less

Mic

roca

thet

er

2.3F

(.0

30”)

The6FENVOY®or6FENVOY® XBiscompatiblewithaPROWLER® SELECT®LPES, PROWLER®14 or PROWLER® 10 microcatheter and an additional device with a maximum outer diameter of 2.9F or less.

Addl

Dev

ice

2.4F

(.0

31”)

or

less

Mic

roca

thet

er

2.8F

(.0

37”)

12657 CNV Bro Envoy Codman BG.indd 2 4/17/09 11:28:21 AM