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` Beyond Tried.
`True.
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`GuideLiner® V3 Catheter
`Guide Extension Catheter With Half-Pipe Technology
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`VWeleflex:
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`Beyond ‘Tried. True.
`In 2009, the GuideLiner® Catheter revolutionized the concept of guide extension, creating new
`possibilities in interventional cardiology. Now in its third generation, the GuideLiner® V3 Catheter
`continues to build on a history of innovation and performance—one that's been demonstrated with
`more than half a million catheters in cath labs around the world.’
`
`“The GuideLiner gives me the
`confidence to deliver my chosen
`balloon or stent to almost any
`location.”
`
`— Michael S. Lee, MD, FACC, FSCAI
`
`“The GuideLiner has become an
`indispensable part of my tool kit
`for complex PCI. Simply put, it's
`a game changer.”
`
`of the physician.
`
`Multiple Clinical Uses
`
`MatthewPrice, MD, FACC, FSCAI * These statements reflect the personal experience and opinion
`
`
`Coaxial alignment
`and backup support
`
`Deep-seating for distal
`device delivery
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`Selective delivery
`of contrast
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`1 Data on file.
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`Designed to Perform
`It's not just the proprietary half-pipe technology that sets the GuideLiner® V3 Catheter apart.
`The coil-reinforced extension is specifically designed to enable dependable deep-seating
`for the delivery of interventional devices to distal locations.
`
`Collar
`
`transition
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`
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`Half-pipe
`a
`channel
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`
`
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`Half-Pipe Technology
`The half-pipe channel is designed to minimize
`
`device/collar interaction by directing and aligning
`devices through the collar transition, facilitating
`smooth device entry and seamless delivery.
`
`Half a Million
`Catheters.
`
`0 Reported Collar
`Separations in PCI.’
`
`The half-pipe construction is also
`designed to minimize the opportunity
`for device separation by creating a
`17 cm polymer bond between the
`extension and push rod.
`
`3 Based upon a review of all device experience reports for coronary usage of
`GuideLiner® V3 Catheters from launch through February 13, 2018. Data on file.
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`‘Tortuosity Tested
`From challenging lesions to impossibly acute angles, percutaneous coronary interventions have
`grown more complex. Since being introduced, GuideLiner catheters have been recognized by
`interventionalists as essential tools for addressing difficult anatomies.
`
` Highly Flexible, Coil-Reinforced
`
`
`The GuideLiner® V3 Catheter's coil-reinforced guide extension provides excellent
`flexibility and kink resistance allowing delivery through tortuous vessels to reach -+---++-s++++++0++
`the target area.
`
`Guide Extension
`
`Coil-reinforced guide
`extension is designed to
`maintain luminal integrity
`
`Kink resistant*
`
`
`
`Proximal tab
`
`:
`
`strength and kink resistance
`
` anna Stainless steel push rod for
`
`Zeeseeneene Ribbon wire push rod height (6 Fr.) = 0.012"
`
`4 Data on file.
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`GuideLiner® V3 Catheter Dimensions
`
`
`150 cm
`<—_—_—_—_—_——————————iees
`17 cm Half-pipe |
`108 cm Push rod
`
`
`
`
`25 cm Rapid exchange section
`
`|2mm
`
`Radiopaque
`marker
`
`4mm
`Radiopaque marker
`
`Rapid exchange
`collar transition
`
`White positioning markers at 95 cm (single) & 105 cm (double)
`to assist in placement through the guide
`
`Added Backup Support
`
`With as little as 5 mm of extension, bench testing has shown that the GuideLiner® V3 Catheter
`significantly increases the backup support of a 6 Fr. guide catheter.
`
`200
`
`
`
`
`
`AverageBackupSupport(gf) 150
`
`
`
`i
`
`00
`
`50
`
`
`
`6 Fr. Guide
`
`6 Fr. GuideLiner
`6 Fr. GuideLiner 6 Fr. GuideLiner 6 Fr. GuideLiner
`5mm
`0mm
`10 mm 15 mm
`
`
`7 Fr. Guide
`
`8 Fr. Guide
`
`Testing completed by Vascular Solutions, Inc. Data on file. Comparative data may not be indicative ofclinical performance.
`
`Extension Distance
`
`GuideLiner® V3 Catheter
`GuideLiner® Catheters are intended to be used in conjunction with guide catheters to access discrete regions of the coronary and/or peripheral vasculature, and
`to facilitate placementof interventional devices.
`
`PRODUCT
`RAPID EXCHANGE
`WORKING
`
`
`
`NO. SIZE|REQUIRED GUIDE CATHETER I.D. PUSH ROD O.D.|GUIDE EXTENSION |.D. TIP O.D. LENGTH LENGTH
`
`
`
`5569
`5: Fitts
`5 Fr.
`|.D. 20.056" (1.42 mm)
`0.070" (0.25 mm)
`0.046" (1.17 mm)
`4.0 Fr. (1.35 mm/ 0.053")
`25¢em
`150 em
`
`5570
`5.5) Fis
`6 Fr.
`|.D. 20.066" (1.68 mm)
`0.012” (0.30 mm)
`0.051" (1.30 mm)
`4.8 Fr. (1.60 mm/ 0.063")
`25cm
`150 em
`
`5571
`6 Fr.
`6 Fr. 1.D. 20.070" (1.78 mm)
`0.012" (0.30 mm)
`0.056" (1.42 mm)
`5.1 Fr. (1.70 mm// 0.067")
`25cm
`150 cm
`
`5572
`7 Et
`7 Fr. |.D. 20.078" (1.98 mm)
`0.012" (0.30 mm)
`0.062" (1.57 mm)
`5.7 Fr. 1.90 mm/ 0,075")
`25cm
`150 em
`5573
`8 Fr.
`8 Fr.
`|.D. 20.088" (2.24 mm)
`0.012" (0.30 mm)
`0.071" (1,80 mm)
`6.5 Fr. (216 mm/ 0.085")
`25cm
`150 cm
`
`Packaged in quantities of 1 unit per box.
`
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`Teleflex is a global provider of medical technologies designed to improve the health and quality of people’s lives. We apply
`purpose driven innovation —a relentless pursuit of identifying unmet clinical needs — to benefit patients and healthcare
`providers. Our portfolio is diverse, with solutions in the fields of vascular and interventional access, surgical, anesthesia,
`cardiac care, urology, emergency medicine and respiratory care. Teleflex employees worldwide are united in the under-
`standing that what we do every day makes a difference. For more information, please visit teleflex.com.
`
`Teleflex is the home of Arrow®, Deknatel®, Hudson RCI®, LMA®, Pilling®, Rusch®, and Weck® — trusted brands united by a
`common sense of purpose.
`
`Corporate Office
`Phone +1 610 225 6800, 550 E. Swedesford Road, Suite 400, Wayne, PA 19087, USA
`
`Regional Offices
`United States: Phone +1 919 544 8000, Toll Free 866 246 6990, cs@teleflex.com, 3015 Carrington Mill Boulevard,
`Morrisville, NC 27560, USA
`
`Latin America: Phone +1 919 433 4999, la.cs@teleflex.com, 3015 Carrington Mill Boulevard, Morrisville, NC 27560, USA
`
`International: Phone +353 (0)9 06 46 08 00, orders.intl@teleflex.com, Teleflex Medical Europe Ltd.,
`IDA Business and Technology Park, Dublin Road, Athlone, Co Westmeath, Ireland
`
`Australia 1300 360 226
`Austria +43 (0)1 402 47 72
`
`Belgium +32 (0)2 333 24 60
`Canada +1 (0)800 387 9699
`
`China (Shanghai) +86 (0)21 6163 0965
`China (Beijing) +86 (0)10 6418 5699
`Czech Republic +420 (0)495 759 111
`France +33 (0)5 62 18 79 40
`Germany +49 (0)7151 406 0
`Greece +30 210 6777717
`India +91 (0)44 2836 5040
`
`Italy +39 0362 58911
`Japan +81 (0)3 6632 3600
`
`Korea +82 2536 7550
`Mexico +52 55 5002 3500
`
`Netherlands +31 (0)88 00 215 00
`New Zealand 0800 601 100
`
`Poland +48 22 4624032
`Portugal +351 22541 90 85
`Singapore (SEA non-direct sales countries) +65 6439 3000
`Slovak Republic +421 (0)3377 254 28
`South Africa +27 (0)11 807 4887
`Spain +34 918 300 451
`Switzerland +41 (0)31 818 40 90
`
`United Kingdom +44 (0)1494 53 27 61
`For more information, please visit teleflex.com.
`
`Please see the Instructions for Use for a completelisting of the indications, contraindications, warnings and precautions.
`CAUTION: Federal Law (U.S.A.) restricts this device to sale by or on the order of a physician.
`
`Teleflex, the Teleflex logo, Arrow, Deknatel, GuideLiner®, Hudson RCI, LMA,Pilling, Rusch, and Weck are trademarks or registered trademarks of Teleflex
`Incorporatedor its affiliates, inthe U.S. and/or other countries.
`
`Information in this material is not a substitute for the product Instructions for Use. Notall products may be available in all countries. Please contact your
`local representative. Revised: 02/2018.
`
`© 2018 Teleflex Incorporated. All rights reserved. MC-003856 Rev 0.1
`
`‘VWeleflex:
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`VSIMDT00003670
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