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Refer to the Instructions for Use for a complete listing of the indications, contraindications, warnings and precautions. Information in this material is not a substitute for the product Instructions for Use.

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.
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 peripheral vascular disease, as evidenced by 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 or infection of the target site is suspected.
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 1) anchor catching on the bifurcation or being positioned incorrectly, and/or 2) 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 depth 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 (BMI >40 kg/m2 or <20 kg/m2).
Do not use if the patient has post-procedure blood pressure >180 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 or nickel.

PRECAUTIONS:
The MANTA Device should only be used by a licensed physician or healthcare provider trained in the use of this device.

This device contains a small radiopaque stainless-steel lock that is implanted in the puncture tract. See MRI information in these instructions for use and patient implant card. In the event that bleeding from the femoral access site persists after the use of the MANTA Device, the physician should assess the situation. Based on the physician assessment of the amount of bleeding, use manual or mechanical compression, application of balloon pressure from a secondary access site, placement of a covered stent, and/or surgical repair to obtain hemostasis. 

ADVERSE EVENTS:
The following potential adverse events related to the deployment of Vascular Closure Devices have been identified:
Ischemia of the leg or stenosis of the femoral artery.
Local trauma to the femoral or iliac artery wall, such as dissection.
Retroperitoneal bleeding, and its consequences, as a result of failed closure in the setting of an access above the inguinal ligament or the most inferior border of the epigastric artery (IEA).
Perforation of iliofemoral arteries, causing bleeding/hemorrhage.
Thrombosis formation or embolism.
Adjacent nerve damage or neuropathy.
Other access site complications leading to bleeding, hematoma, pseudoaneurysm, or arterio-venous fistula, possibly requiring blood transfusion, surgical repair, and/or endovascular intervention.

Potential Adverse Events associated with any large bore intervention, including the use of the MANTA Vascular Closure Device, include but are not limited to:
Arterial damage
Arterio-venous fistula
Bradycardia
Compartment syndrome
Death related to the procedure
Deep vein thrombosis
Ecchymosis
Edema
Infection at the puncture site which may require antibiotics or extended hospitalization
Inflammatory response
Late arterial bleeding
Oozing from the puncture site
Pressure in groin/access site region
Vessel laceration or trauma
Wound dehiscence

The Ringer™ Perfusion Balloon Catheter (PBC) is indicated for balloon dilatation of coronary artery or coronary bypass graft stenoses where the physician desires distal blood perfusion during balloon inflation for the purpose of improving myocardial perfusion.

The GuideLiner™  Catheters are intended to be used in conjunction with guide catheters to access discrete regions of the coronary and/ or peripheral vasculature, to facilitate placement of interventional devices, and to assist in crossing de novo coronary chronic total occlusions (CTO). GuideLiner™ V3 Catheters are indicated for CTO in the US only. The GuideLiner™ Coast™ Catheter is indicated for CTO in the US and Canada. The GuideLiner™ Catheters are contraindicated in vessels less than 2.5mm in diameter and in vessels in the neurovasculature or the venous system.

The Turnpike™ Catheters are intended to be used to access discrete regions of the coronary and/or peripheral vasculature. They may be used to facilitate placement and exchange of guidewires and to subselectively infuse/deliver diagnostic and therapeutic agents, and to assist in crossing de novo coronary chronic total occlusions (CTO).

Refer to the Instructions for Use for a complete listing of the indications, contraindications, warnings and precautions. Information in this material is not a substitute for the product Instructions for Use.

CAUTION: Federal (USA) law restricts these devices to sale or use by or on the order of a physician.

Teleflex, the Teleflex logo, Coast, GuideLiner, MANTA, Ringer, and Turnpike are trademarks or registered trademarks of Teleflex Incorporated or its affiliates in the U.S. and/or other countries. Other names are the trademarks or registered trademarks of their respective owners. Refer to the Instructions for Use for a complete listing of the indications, contraindications, warnings, and precautions. Information in this material is not a substitute for the product Instructions for Use. Not all products may be available in all countries. Please contact your local representative. 

© 2025 Teleflex Incorporated. MC-010767 Rev 0. Revised 05/2025.