Peripheral Products arşivleri - Aventin Health https://aventinhealth.com/en/ Cardiac Rhythm Management, Heart Failure Fri, 14 Jan 2022 08:44:03 +0000 en-US hourly 1 https://wordpress.org/?v=5.9.1 https://aventinhealth.com/wp-content/uploads/2022/01/cropped-aventin-favicon-02-32x32.png Peripheral Products arşivleri - Aventin Health https://aventinhealth.com/en/ 32 32 Protégé™ EverFlex™ | Biliary Stenting https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/protege-everflex-biliary-stenting/ https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/protege-everflex-biliary-stenting/#respond Fri, 14 Jan 2022 08:44:03 +0000 https://aventinhealth.com/urunler/uncategorized/protege-everflex-biliary-stenting/

When your job requires the 5mm size, choose the Protégé™ EverFlex™ self-expanding bile stent system to deploy the same reliable stent.

Protégé™ EverFlex™ | Biliary Stenting yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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PRODUCT DETAILS

DURABILITY

Durability of Protégé EverFlex Self-expanding Biliary Stent
  1. The spiral cell connection model increases flexibility.
  2. The three wave top design generates expansion force that resists compression and provides excellent wall conformation.
  3. Top-to-top tie knots help distribute the force evenly between the four struts.
  4. Tantalum markers for improved visibility and easier, more precise positioning.
  5. The flexible design increases fracture resistance and restores vessel patency.

PRECISE PLACEMENT

Precision Placement with Protégé EverFlex Self-expanding Biliary Stent
  1. Tantalum GPS markers increase visibility for easier and more precise positioning.
  2. Proprietary deployment system secures the stent to prevent premature deployment or “skip”.

EASE

  • The system has the widest stent lengths: 20 mm – 120 mm.
  • All series 6 F cases are compatible.

Protégé™ EverFlex™ | Biliary Stenting yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/protege-everflex-biliary-stenting/feed/ 0 Protégé™ GPS™ | Self-expanding Peripheral and Biliary Stenting https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/protege-gps-self-expanding-peripheral-and-biliary-stenting/ https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/protege-gps-self-expanding-peripheral-and-biliary-stenting/#respond Fri, 14 Jan 2022 08:41:28 +0000 https://aventinhealth.com/urunler/uncategorized/protege-gps-self-expanding-peripheral-and-biliary-stenting/

Choose the Protégé™ GPS™ self-expanding peripheral stent system if your job depends on precision, radial strength, and flexibility in the treatment of lesions in the common or external iliac arteries, subclavian arteries, or the biliary system.

Protégé™ GPS™ | Self-expanding Peripheral and Biliary Stenting yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MARKERS

ENVIRONMENTAL

The stent is indicated for use in the following types of occlusion or lesion:

  • Obstructions or lesions at high risk for sudden closure or threatened closure following percutaneous transluminal angioplasty (PTA)
  • Lesions in the common iliac, external iliac, or subclavian arteries appearing at high risk for restenosis following PTA

Stenting aims to improve and maintain the arterial lumen diameter.

BILIARY

The stent is intended as a palliative treatment of malignant neoplasms in the biliary tree.

Not all indications for the PROTÉGÉ GPS SELF EXPANDING PERIPHERAL AND BLADE STENT have been validated globally, please refer to the complete Directions for Use guide for the approved indication for Use in your geography.

PRODUCT DETAILS

LARGE DIAMETER / LOW PROFILE

  • Dimensions up to 14 mm allow you to overcome great challenges.
  • Low profile: Full line 6 F compatible.

PRECISE PLACEMENT

Precision Placement with Protégé GPS
  1. Tantalum GPS markers increase visibility for easier and more precise positioning.
  2. Proprietary deployment system secures the stent to prevent premature deployment or “skip”.

RADIAL STRENGTH AND FLEXIBILITY

  • Designed for radial strength without sacrificing flexibility.

Protégé™ GPS™ | Self-expanding Peripheral and Biliary Stenting yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/protege-gps-self-expanding-peripheral-and-biliary-stenting/feed/ 0 ParaMount™ Mini GPS™ | Balonla Genişletilebilir Periferik Stent Sistemi https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/paramount-mini-gps-balonla-genisletilebilir-periferik-stent-sistemi/ Fri, 14 Jan 2022 08:38:25 +0000 https://aventinhealth.com/urunler/uncategorized/paramount-mini-gps-balonla-genisletilebilir-periferik-stent-sistemi/

See the right stent placement path when you choose the ParaMount™ Mini GPS™ balloon expandable peripheral stent system with radiopaque markers that increase visibility before, during and after stent placement. The system's low profile is designed for flexibility and easy navigation to target lesions in the kidney anatomy and as a palliative therapy in the biliary tree.

ParaMount™ Mini GPS™ | Balonla Genişletilebilir Periferik Stent Sistemi yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MARKERS

ENVIRONMENTAL

The ParaMount Mini GPS balloon expandable peripheral stent is indicated for use in occlusions, lesions at high risk of sudden closure or threatened closure after percutaneous transluminal angioplasty (PTA), or lesions believed to be at high risk of stenosis following PTA in the renal arteries. Stenting aims to improve and maintain the arterial lumen diameter.

BILIARY

The ParaMount Mini GPS balloon expandable peripheral stent is indicated for use as the palliative treatment of malignant neoplasms in the biliary tree.

Not all indications for the PARAMOUNT MINI GPS BALLOON EXPANDABLE PERIPHERAL AND BALLAIY STENT have been validated globally, please refer to the complete Directions for Use guide for approved Use indication in your geography.

PRODUCT DETAILS

HIGH VISIBILITY

  • GPS radiopaque tantalum markers are embedded at each end of the stent for improved procedural accuracy and visibility.
  • GPS marks define the near and far edges as the stent expands.
  • GPS technology ensures that the stent remains visible under fluoroscopy to confirm stent placement.
Location of GPS radiopaque markers on the end of a Paramount Mini GPS stent.

GPS Markers

Position of GPS radiopaque markers at the end of the ParaMount Mini GPS stent.

LOW PROFILE SYSTEM

  • Available on a 0.014″ and 0.018″ guidewire compatible balloon catheter.
  • Compatible with 6 F or 7 F guide catheter.
  • It is designed for flexibility when traveling to a target lesion.

STRENGTH AND FLEXIBILITY

  • The unique cell geometry provides greater radial strength and support.

SENSITIVE

  • Medtronic’s proprietary Micro-Grip™ technology ensures proper centering of the stent prior to expansion.
  • Stent shows minimal shortening at recommended expansion diameters

ParaMount™ Mini GPS™ | Balonla Genişletilebilir Periferik Stent Sistemi yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> IN.PACT™ Admiral™ | Paclitaxel and Drug Coated Balloon https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/in-pact-admiral-paclitaxel-and-drug-coated-balloon/ Fri, 14 Jan 2022 08:32:09 +0000 https://aventinhealth.com/urunler/uncategorized/in-pact-admiral-paclitaxel-and-drug-coated-balloon/

The IN.PACT™ Admiral™ drug-coated balloon (DCB) is a clinically proven, primary endovascular therapy that treats femoropopliteal disease, reducing reinterventions and preserving future treatment options. IN.PACT Admiral DCB is indicated for de novo restenotic. or in-stent restenotic lesions up to 360 mm with a reference vessel diameter of 4 to 7 mm in the superficial femoral or popliteal arteries.

IN.PACT™ Admiral™ | Paclitaxel and Drug Coated Balloon yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MEDICATION COATED BALLOON

For the treatment of femoropopliteal disease in which 75% of patients do not require re-intervention at 5 years. This is more important now than ever.†

IN.PACT Admiral drug-coated balloon shown in 150, 200, and 250 mm lengths

NOW SUPPORTED BY 5-YEAR AND GLOBAL WORKING DATA

For treatment of femoropopliteal disease with 75% of patients reintervention-free at 5 years.1 This matters now more than ever.†

Maintain long-term patency with the IN.PACT Admiral drug-coated balloon (DCB); this provides durable, consistent and safe results across multiple clinical trials as well as complex patient and lesion types. With more than 3,500 patients enrolled in 21 clinical trials and more than 500,000 patients treated worldwide, the IN.PACT Admiral balloon is the market-leading DCB for the treatment of femoropopliteal disease.
IN.PACT Admiral DCB is a clinically proven primary endovascular therapy that treats femoropopliteal disease, reducing interventions and preserving future treatment options.

DURATION OF PACLITAXEL IN TISSUE

Only IN.PACT Admiral DCB releases drug into tissue through the restenotic window.

Only the IN.PACT Admiral drug-coated balloon releases drug into the tissue through the restenotic window

Feature Features
Paclitaxel Drug Dosage 3.5 µg/mm 2
Excipient Urea
Balloon Diameters 4.0 to 7.0 mm
Balloon Sizes 40, 60, 80, 120, 150, 200, and 250 mm ll
Balloon Fold Configurations 4.0 mm: 3 folds; 5.0, 6.0, and 7.0 mm: 6 folds
Catheter Design Over-the-wire (OTW)
Catheter Lengths 80 and 130 cm
Guidewire Compatibility 0.035 in

IN.PACT™ Admiral™ | Paclitaxel and Drug Coated Balloon yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> Visi-Pro™ | Balloon Expandable Peripheral and Biliary Stenting https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/visi-pro-balloon-expandable-peripheral-and-biliary-stenting/ Fri, 14 Jan 2022 08:28:02 +0000 https://aventinhealth.com/urunler/uncategorized/visi-pro-balloon-expandable-peripheral-and-biliary-stenting/

Provide visibility before and after stenting with the Visi-Pro™ balloon expandable peripheral stent system for the treatment of peripheral artery disease (PAD). The patented design of the stent balances strength and flexibility for the proven patency found in the VISIBILITY ILIAC study. Radiopaque markings on the stent ensure precise placement. Deliver more than 0.035 inches of guidewire for use in the common iliac, external iliac, and subclavian arteries as indicated for the palliative treatment of malignant neoplasms in the biliary tree.

Visi-Pro™ | Balloon Expandable Peripheral and Biliary Stenting yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MARKERS

ENVIRONMENTAL

The Visi-Pro balloon-expandable peripheral stent is indicated for use in occlusions, lesions at high risk of sudden closure after percutaneous transluminal angioplasty (PTA), or lesions believed to be at high risk of post-PTA stenosis in the following arteries:

  • Common and external iliac, subclavian
  • Kidney

Stenting aims to improve and maintain the arterial lumen diameter.

BILIARY

The Visi-Pro balloon expandable peripheral stent is indicated for use as the palliative treatment of malignant neoplasms in the biliary tree. Not all indications for the VISI-PRO BALLOON EXPANDABLE PERIPHERAL AND BILIARY STENT have been validated globally, please refer to the complete Directions for Use guide for approved Use indication in your geography.

PRODUCT DETAILS

PREMIUM GÖRÜNÜRLÜK

  • Distinctive 0.035′ balloon expandable stent with radiopaque markings provides visibility during and after stent placement.

SOLID RADIAL STRENGTH AND FLEXIBILITY

  • Patented design balances strength and flexibility.

PRECISE PLACEMENT

  • Minimal dilatation of healthy tissue is dependent on balloon-to-stent placement.
  • Provides correct catheter marker alignment to balloon taper.
  • The progressive stent design provides minimal shortening.

Visi-Pro™ | Balloon Expandable Peripheral and Biliary Stenting yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> Chocolate™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/chocolate-pta-balloon-catheter-percutaneous-transluminal-angioplasty/ Fri, 14 Jan 2022 07:47:58 +0000 https://aventinhealth.com/urunler/uncategorized/chocolate-pta-balloon-catheter-percutaneous-transluminal-angioplasty/

The only nitinol caged balloon with Controlled Dilation, the Chocolate™* PTA balloon is designed for 1:1 vessel size to minimize flow-limiting dissections and reduce recoil.

As the balloon inflates, the cage causes the balloon to form a series of segmented cushions and grooves throughout the entire lesion. Cushions apply force to create small dissections necessary for effective dilation. Grooves relieve stress and stop dissections from spreading.

Chocolate™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MARKERS

The Chocolate™* PTA Balloon Catheter is designed for balloon dilation of lesions in the peripheral vasculature, including the iliac, femoral, ilio-femoral, popliteal, infra-popliteal and renal arteries.

PRODUCT DETAILS

The Chocolate PTA balloon is a semi-conforming balloon enclosed in a nitinol-restrictive structure or cage that allows 1:1 vessel size.

The cage and balloon expand simultaneously so that as the balloon opens, the cage prevents the balloon from catching on lesions and causing torsional stress and dissections.

During inflation, the cage causes the balloon to expand in a controlled manner, reducing dog bones and over-inflation. The mesh also causes the balloon to form a series of segmented cushions and grooves throughout the entire lesion. Cushions apply force to create small dissections necessary for effective dilation. Grooves relieve stress and stop dissections from spreading.

Chocolate PTA Balloon Catheter Design

Chocolate PTA Balloon with Controlled Dilatation
  1. INFLATION: During inflation, the cage causes the balloon to form a series of segmented cushions and grooves across the entire lesion.
  2. BALLOON: The balloon is kept in the cage during inflation, preventing the dogs’ bones from swelling and protecting healthy tissue.
  3. CAGE: The nitinol cage expands with the balloon, protecting the vessel from torsional stresses and minimizing dissections.
  4. PILLOWS: Cushions apply force to create small dissections necessary for effective dilation.
  5. Grooves: Grooves relieve tension and stop dissections from spreading.

Chocolate™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> EverCross™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/evercross-pta-balloon-catheter-percutaneous-transluminal-angioplasty/ Fri, 14 Jan 2022 07:45:24 +0000 https://aventinhealth.com/urunler/uncategorized/evercross-pta-balloon-catheter-percutaneous-transluminal-angioplasty/

Push and follow difficult lesions with the EverCross™ OTW PTA balloon catheter, the power of balloons for use in your above-knee interventions. Choose from a wide range of sizes available to treat peripheral arterial disease (PAD) in a variety of vessel sizes and lesion types.

EverCross™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MARKERS

The EverCross 0.035” OTW PTA dilatation catheter is designed to dilate stenoses in the iliac, femoral, ilio-femoral, popliteal, infrapopliteal and renal arteries and for the treatment of obstructive lesions of natural or synthetic arteriovenous dialysis fistulas. This device is also indicated for post-stent dilatation in the peripheral vasculature.

PRODUCT DETAILS

  • Flexible materials at the distal end of the catheter provide excellent tracking in curved anatomy.
  • Proprietary catheter coating maintains lubricity and reduces drying.
  • Robust shank design provides buckle-resistant pushability.
  • The Bevel 360™ tip provides a smooth transition to the wire and, together with a low-profile catheter, facilitates passage.

EverCross™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> Admiral Xtreme™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/admiral-xtreme-pta-balloon-catheter-percutaneous-transluminal-angioplasty/ Fri, 14 Jan 2022 07:43:35 +0000 https://aventinhealth.com/urunler/uncategorized/admiral-xtreme-pta-balloon-catheter-percutaneous-transluminal-angioplasty/

Treat longer PAD lesions above the knee with the Admiral Xtreme™ PTA balloon catheter. Also available in 250 and 300 mm lengths with 0.035" guide wire compatibility, with large inflation lumen for rapid inflation and deflation.

Admiral Xtreme™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MARKERS

Admiral Xtreme is indicated for percutaneous transluminal angioplasty (PTA) in patients with obstructive disease of the peripheral arteries.

CONTRAINDICATIONS

The Admiral™ Xtreme PTA catheter is contraindicated for use in the coronary arteries and supraaortic vessels. It is also contraindicated when the target lesion cannot be crossed with a guidewire.

PRODUCT DETAILS

LONG BALLOON LENGTHS

  • Balloon lengths of 250 and 300 mm are available for single dilation of long lesions.
  • Proprietary technology prevents banana-shaped bubble.

COAXIAL DOUBLE LUMEN SHAFT DESIGN

  • Strong pushability and bending resistance combined with flexibility.
  • Offers support for contralateral maneuvers.
  • Wide inflation lumen provides rapid inflation and deflation.

LOW BALLOON PROFILE

  • It shows good refolding behavior.
  • Confidently cross lesions.

HYDROPHILIC COATING

  • It makes the transition easy.

FLEXITEC XTREME BALLOON MATERIAL

  • The balloon wall thickness is reduced.
  • Flexitec™ offers scratch resistance.
  • Provides high rated burst pressure.

Admiral Xtreme™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> Fortrex™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/fortrex-pta-balloon-catheter-percutaneous-transluminal-angioplasty/ Fri, 14 Jan 2022 07:40:30 +0000 https://aventinhealth.com/urunler/uncategorized/fortrex-pta-balloon-catheter-percutaneous-transluminal-angioplasty/

Deliver high-pressure, targeted therapy to challenging lesions with the Fortrex™ 0.035" OTW PTA balloon catheter, a balloon engineered and engineered for peak performance at nominal burst pressure. Choose Fortrex high pressure PTA balloon catheters when you need AV access or arterial intervention. balanced thrust and travel, optimal balloon shape retention at nominal burst pressure, and a best-in-class tip entry profile.

Fortrex™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MARKERS

The Fortrex 0.035” OTW PTA balloon catheter is designed to dilate stenoses in the iliac, femoral, iliofemoral, popliteal, infra-popliteal and renal arteries and for the treatment of obstructive lesions of natural or synthetic arteriovenous dialysis fistulas. This device is also indicated for post-stent dilatation in the peripheral vasculature.

PRODUCT DETAILS

DELIVERY

  • The low-end input profile provides tight tracking to the wire.
  • The robust, flexible shaft design facilitates successful navigation on winding vessels.

PREDICTABILITY

  • The balloon material and design allow it to retain its shape at nominal burst pressure.
  • Focus pressure is applied to the lesion for controlled, targeted therapy.

PROCEDURE EFFICIENCY

  • The balloon material and wall thickness allow reliable rewrapment and reliable reinsertion of the balloon into the sheath.
  • The rapid deflation time contributes to the reduction of the procedure length.
Design of Fortrex PTA Balloon

Fortrex PTA Balloon Design

  1. The shaft provides optimum thrust and track balance.
  2. Balloon material offers optimum shape retention at nominal burst pressure.
  3. Low end entry profile provides tight tracking on the wire.

Fortrex™ PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

]]> Pacific™ Plus PTA Balloon Catheter | Percutaneous Transluminal Angioplasty https://aventinhealth.com/en/urunler/medtronic-products/peripheral-products/pacific-plus-pta-balloon-catheter-percutaneous-transluminal-angioplasty/ Fri, 14 Jan 2022 07:40:28 +0000 https://aventinhealth.com/urunler/uncategorized/pacific-plus-pta-balloon-catheter-percutaneous-transluminal-angioplasty/

Realize more access options when you choose the Pacific™ Plus PTA balloon catheter OTW 0.018" with versatile shaft lengths. Proprietary balloon technology allows for improved passage for treatment of lesions and improved shaft design accelerates deflation following treatment.

Pacific™ Plus PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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MARKERS

The Pacific™ Plus PTA Catheter is intended to dilate stenoses in the iliac, femoral, iliofemoral, popliteal, infrapopliteal, and renal arteries; and for the treatment of occlusive lesions of natural or synthetic arteriovenous dialysis fistulas.

CONTRAINDICATIONS

The Pacific Plus PTA catheter is contraindicated for use in the coronary arteries or neurovasculature. It is also contraindicated when the guidewire does not pass the target lesion.

 

PRODUCT DETAILS†

  • Shaft lengths 90, 130, 180 cm compatible with 0.014″ and 0.018″ provide more access options.
  • Advanced rewind technology provides multiple inflations.
  • Rapid deflation can contribute to shorter processing times.
  • Low-compliant balloon material addresses various lesions.
  • Offers complementary dimensions for Pacific™ Xtreme.*

EXCELLENT PASSABILITY TO IMPROVE LESION TRANSITION

  • The hydrophilic coating on the shaft contributes to crossability.
  • Low profile provides high crossability.†

Pacific™ Plus PTA Balloon Catheter | Percutaneous Transluminal Angioplasty yazısı ilk önce Aventin Health üzerinde ortaya çıktı.

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