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USA / Product Areas / Interventional Go Browse our Interventional Cardiology/Radiology Products / United States ( change ) Bone Access Arrow ® OnControl ® Powered Bone Access System Cardiac Assist AC3 Optimus™ Intra-Aortic Balloon Pump Intra Aortic Balloon Catheters Cardiac Diagnostics Arrow ® Balloon Wedge Pressure Catheters Arrow ® Thermodilution Catheters Arrow ® Berman Angiographic Catheters Arrow ® Temporary Pacing Catheters and Kits Coronary Interventions Chocolate XD ® PTCA Balloon Catheter GuideLiner ® V3 Catheter TrapLiner ® Catheter Turnpike ® Catheters Twin-Pass ® Dual Access Catheters SuperCross ™ Microcatheters Venture ® 0.014″ Catheters Guidewires Minnie ® Support Catheter Micro Elite ™ Snare Guardian ® II Hemostasis Valve Pronto ® Extraction Catheters Drainage Arrow ® Diagnostic & Drainage Products Drainer ® Centesis Catheter Hemodialysis Arrow-Clark ™ VectorFlow ® Chronic Hemodialysis Catheter Arrow ® NextStep ® Chronic Hemodialysis Catheter Arrow ® Cannon ® II Plus Chronic Hemodialysis Catheter Arrow Edge ® Chronic Hemodialysis Catheter Arrow Simplicity ® Micro-Introducer Sets Hemostasis and Embolization D-Stat ® Dry & Thrombix ® Topical Hemostat D-Stat ® Flowable Hemostat D-Stat ® Rad-Band Topical Hemostat Gel-Bead ™ Embolization Spheres Gel-Block ™ 10X Embolization Pledgets Hunter ™ Biopsy Sealing Device ThrombiDisc ™ Topical Hemostat Peripheral Interventions Turnpike ® Catheter Guidewires Piggyback ® Wire Converter Minnie ® Support Catheter Elite ™ Snares Guardian ® II Hemostasis Valve Pronto ® Extraction Catheters Structural Heart Interventions Langston ® Dual Lumen Catheters Wattson™ Temporary Pacing Guidewire Thrombectomy Pronto ® Extraction Catheters Vascular Access and Closure MANTA ® Vascular Closure Device Super Arrow-Flex ® Sheaths Arrow ® Percutaneous Sheath Introducers Arrow ® Radial Access Sheath Kits GrebSet ® Micro-Introducer Kit VSI StraitSet ® Micro-Introducer Kit VSI Micro-Introducer Kits ™ VSI Micro-HV Introducer Kits ™ VSI Pedal Micro-Introducer Kit ™ OptiSeal ® Valved Peelable Introducer Vasc Band ™ Hemostat Accumed ™ Wrist Positioning Splint Spotlight Be in control with OnControl ® - the trusted powered biopsy solution MANTA ® Vascular Closure Device - designed for large bore closure Learn about TrapLiner ® , the guide extension catheter with trapping capabilities View the Interventional E-Commerce Site and Catalog Do you have a medical device idea? Let us know! Learn more about the Chocolate XD ® PTCA Balloon Catheter About Teleflex Interventional Innovations to Simplify Interventions. As the interventional cornerstone of Teleflex, we offer a growing portfolio of specialty-focused solutions to support interventionalists around the globe. Our products are known for their innovative ability to simplify complex procedures and common clinical challenges. Teleflex Interventional Ordering Catalog » Product Patents » Upcoming Events & OnDemand Webinars TCT 2023 October 23 – 26 San Francisco, CA SCAI 2023 Fellows Courses December 1 – 5 Miami, FLA Webinars OnDemand: 5/18/23 Teleflex Tackles Tough Cases with Dr. Rhian Davies and Dr. Brian Jefferson Watch Now 3/30/23 Teleflex Tackles Tough Cases with Dr. Saroj Neupane and Dr. Lorenzo Azzalini Watch Now Clinical Investigations A clinical investigation related to percutaneous coronary interventions is planned to be conducted under the exception from informed consent regulations in select cities. To learn more and provide feedback, please visit ringerinvestigation.com Clinical Support Hotlines IABP: USA: 800-447-IABP 24/7 (Current IABP Customers) International: 978-250-5177 All other products: 888-413-3104 General Customer Service and Support Email Customer Service Contact Us Form Product Orders (866) 246-6990 USA Product orders by FAX: (866) 804-9881 USA Please see the instructions for use for complete product information. CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician. Not all products are available in all regions. Please contact customer service to confirm availability in your region. MANTA VASCULAR CLOSURE DEVICE INDICATIONS FOR USE: The MANTA Vascular Closure Device is indicated for closure of femoral arterial access sites while reducing time to hemostasis following the use of 10-20F devices or sheaths (12-25F OD) in endovascular catheterization procedures. CONTRAINDICATIONS: There are no known contraindications to the use of this device. WARNINGS: Do not use if the puncture site is proximal to the inguinal ligament or above the most inferior border of the epigastric artery (IEA), as this may result in retroperitoneal bleeding. Do not use in patients with severe calcification of the access vessel and/or common femoral artery stenosis resulting in a vessel 5mm in diameter for the 14F MANTA or 6mm in diameter for the 18F MANTA, or 50% diameter femoral or iliac artery stenosis. Do not use if the target common femoral artery lumen is 5mm for the 14F MANTA or 6mm for the 18F MANTA, whether due to intrinsic vessel size or stenosis from any cause. Do not use in the presence of an ipsilateral femoral or iliac artery stenosis resulting in 50% diameter reduction. Do not use in patients with severe peripheral vascular disease, as evidenced by severe claudication when ambulating 100 feet, weak or absent pulses in the affected limb, or ABI 0.5 at rest. Do not use if the temperature indicator dot on package has changed from light gray to dark gray or black. Do not use if the package is damaged or any portion of the package has been previously opened. Do not use if the items in the package appear damaged or defective in any way Do not REUSE or RESTERILIZE. The MANTA Device is single use only. The MANTA Device contains bioresorbable materials that cannot be reused or re-sterilized. Reuse or re-sterilization may cause degradation to the integrity of the device, leading to device failure which may result in patient injury, illness, or death. Do not use the MANTA Device where bacterial contamination of the procedure sheath or surrounding tissues may have occurred, as this may result in infection. Do not use if there is substantial bleeding around the Depth Locator at the access site during the Depth Location procedure, as this may result in an inaccurate measurement. Do not use if the MANTA delivery system becomes kinked. Do not inflate a contralateral balloon in the femoral or iliac artery during MANTA Sheath exchange or the MANTA Closure procedure. Do not use MANTA if there has been a femoral artery puncture in same vessel within the prior 30 days, recent femoral artery puncture in same groin that has not healed appropriately, and/or recent (30 days) vascular closure device placement in same femoral artery. Do not use if the puncture site is at or distal to the bifurcation of the superficial femoral and profunda femoris artery, as this may result in the (a) anchor catching on the bifurcation or being positioned incorrectly, and/or (b) collagen deposition into the vessel. Do not use if there is difficult dilation from initial femoral artery access (e.g., damaging or kinking dilators) while step dilating up to the large-bore device. Difficult dilation of the puncture tract due to scar tissue may lead to swelling of surrounding tissue, thus compromising the accuracy of the puncture depth determined during the puncture location procedure. Do not use if sheath insertion is in a vessel other than the femoral artery. Do not use if there is marked tortuosity of the femoral or iliac artery. Do not use if the patient has marked obesity or cachexia (BMI40 kg/m 2 or 20 kg/m 2 ). Do not use if the patient has post-procedure blood pressure180 mmHg that cannot be lowered prior to access site closure. Do not use in patients who cannot be adequately anticoagulated for the procedure. Do not use the MANTA Device in patients with known allergies to bovine products, collagen and/or collagen products, polyglycolic or polylactic acid polymers, stainless steel...