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Coding CTO DES Hypertension Imaging Modalities PCI Pharmacology Radial Regulatory Structural Disease Valvular Interventions

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US Company Directory


Medtronic

710 Medtronic Parkway, Minneapolis, MN 55432-5604

PHONE: (763) 514-4000 | FAX: (763) 514-4879

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Balloons / PTCA Balloons

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Company Name Product Name Nominal Pressure (atm) Rated Burst Pressure (atm) Guidewire Compatibility (inch) Shaft Length (cm) Sheath Compatibility (F) Balloon Diameters (mm) Balloon Lengths (mm) Comments
Medtronic Euphora 8 14 0.014 142 5, 6 1.5, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4 6, 10, 12, 15, 20, 25, 30 –
Medtronic NC Euphora 12 20 0.014 142 5, 6 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.5, 5 6, 8, 12, 15, 20, 27 –
Medtronic NC Sprinter RX 10 18 0.016 142 5 (2–4 mm balloons), 6 (4–5 mm balloons) 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.5, 5 6, 9, 12, 15, 21, 26 –
Medtronic Sprinter Legend RX 6 (1.5 mm) 12 (1.5 mm) 0.016 142 5, 6 (kissing-balloon technique compatible) 1.5 6, 10, 12, 15, 20 –
Medtronic Sprinter Legend RX 8 (2–4 mm) 14 (2–4 mm) 0.016 142 5, 6 (kissing-balloon technique compatible up to 3.5-mm balloon) 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4 6, 10, 12, 15, 20, 25, 30 –
Medtronic Sprinter OTW 6 (1.5 mm) 12 (1.5 mm) 0.016 138 5, 6 1.5 6, 10, 12, 15, 20 –
Medtronic Sprinter OTW 8 (2–4 mm) 14 (2–4 mm) 0.016 138 5, 6 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4 6, 10, 12, 15, 20, 25, 30 –
Medtronic 1.25-mm Sprinter Legend 12 (1.25 mm) 12 (1.25 mm) 0.016 RX: 142; OTW: 152 5, 6 (kissing-balloon technique compatible) 1.25 RX: 6, 10, 12, 15, 20; OTW: 6, 10, 15, 20 –

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Catheters / Angiographic Catheters

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Company Name Product Name Type (Braided/Nonbraided) Size (F) Length (cm) Guidewire Compatibility (inch) Radiopaque Tip (Yes/No) Variety of Selective Shapes
Medtronic DxTerity and DxTerity TRA Braided 5, 6 100–125 Up to 0.038 Yes JR, JL, AL, AR, multipurpose, pigtail, specialty (RCB, LCB, IMA, 3DRC, NOTO), universal transradial curves (TRApease, TRAnsformer, TRAcker, TRActive, Ultra)

Catheters / Guiding Catheters

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Company Name Product Name Type (Braided/Nonbraided) Size (F) Length (cm) ID (inch) Radiopaque Tip (Yes/No) Hydrophilic Coating (Yes/No)
Medtronic Launcher Braided 5, 6, 7, 8 47–118 0.058, 0.071, 0.081, 0.090 Yes No
Medtronic Sherpa Braided 6, 7 55–110 0.070, 0.080 Yes No

Catheters / Microcatheters

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Company Name Product Name Type of Catheter Construction Proximal Size (F) Middle Size (F) Distal Size (F) Catheter Working Length (cm) Catheter Endhole ID (inch) Recommended Guidewire Size (inch) Radiopaque Tip (Yes/No) Hydrophilic Coating (Yes/No)
Medtronic Telemark Braided 2.6 1.9 1.4 135, 150 0.020 0.014 Yes Yes

Catheters / Specialty Catheters

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Company Name Product Name Catheter Size (F) Working Length (cm) Minimum Guiding Catheter ID (inch) Comments
Medtronic Telescope Guide Extension Catheter 6 150 0.056 Designed for deliverability with a solid, round pushwire, coil-reinforced distal segment and hydrophilic coating; a soft polymer tip responsively deflects and provides flexibility; and a specially developed on-ramp and entry port allows interventional devices to smoothly pass through the device channel
Medtronic Telescope Guide Extension Catheter 7 150 0.062 Designed for deliverability with a solid, round pushwire, coil-reinforced distal segment and hydrophilic coating; a soft polymer tip responsively deflects and provides flexibility; and a specially developed on-ramp and entry port allows interventional devices to smoothly pass through the device channel

Stents / Coronary Balloon-Expandable Drug-Eluting Stents

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Company Name Product Name Drug Delivered Material Used Polymer Type Maximum Guidewire Size (inch) Introducer Size (F) Stent Diameter (mm) Stent Length (mm) Delivery System Length (cm) US FDA Indicated Use
Medtronic Onyx Frontier Zotarolimus-Eluting Stent System Zotarolimus Shell: cobalt alloy; core: platinum iridium BioLinx biocompatible polymer 0.014 Minimum guide catheter size: 5 2, 2.25, 2.5, 2.75, 3, 3.5, 4, 4.5, 5 8, 12, 15, 18, 22, 26, 30, 34, 38 (2-mm diameter not available in 34-, 38-mm lengths; 4.5-, 5-mm diameters not available in 8-, 34-, 38-mm lengths) 140 Non-left main bifurcation lesions using the provisional technique; chronic total occlusions; patients with diabetes mellitus; high bleeding risk patient indication with 1 month DAPT labeling
Medtronic Resolute Onyx Zotarolimus-Eluting Stent System Zotarolimus Shell: cobalt alloy; core: platinum iridium BioLinx biocompatible polymer 0.014 Minimum guide catheter size: 5 2, 2.25, 2.5, 2.75, 3, 3.5, 4, 4.5, 5 8, 12, 15, 18, 22, 26, 30, 34, 38 (2 mm not available in 34-, 38-mm lengths; 4.5, 5 mm not available in 8-, 34-, 38-mm lengths) RX: 140; OTW: 140 Non-left main bifurcation lesions using the provisional technique; chronic total occlusions; patients with diabetes mellitus; high bleeding risk patient indication with 1 month DAPT labeling

Valves / Interventional Preshaped Wires

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Company Name Product Name Diameter (inch) Length (cm) Coating Tip Type Curve Size Comments
Medtronic Confida Brecker Guidewire 0.035 260 PTFE Continuous, tapered core 30 mm Precurved for left ventricle placement

Valves / Transcatheter Aortic Valve Replacement

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Company Name Product Name Valve Diameter (mm) Valve Height (mm) Valve Annulus Size Range (mm) Valve Frame Material Valve Leaflet Material Valve Anticalcification Process Delivery System Name Delivery Access Delivery System Deployment Type Delivery System Size (F) Delivery System Working Length (cm) US FDA Indicated Use Comments
Medtronic CoreValve Evolut R Transcatheter Aortic Valve Replacement System 23, 26, 29, 34 45 17/18–30 (CT derived diameters, 17 for TAV-in-SAV only) Nickel titanium (nitinol) Porcine pericardium Yes EnVeo Pro Delivery System Transfemoral, direct aortic, subclavian Self expanding 14 equivalent/6 mm (23, 26, 29 mm); 16 equivalent/6.7 mm (34 mm) 107 Indicated for relief of aortic stenosis in patients with symptomatic heart disease due to severe native calcific aortic stenosis who are judged by a heart team, including a cardiac surgeon, to be appropriate for the transcatheter heart valve replacement therapy and for use in patients with symptomatic heart disease due to failure (stenosed, insufficient, or combined) of a surgical bioprosthetic aortic valve who are judged by a heart team, including a cardiac surgeon, to be at high or greater risk for open surgical therapy (ie, STS predicted risk of operative mortality score ≥ 8% or at a ≥ 15% risk of mortality at 30 days) –
Medtronic Evolut FX Transcatheter Aortic Valve Replacement System 23, 26, 29, 34 45 17/18–30 (CT derived diameters, 17 for TAV-in-SAV only) Nickel titanium (nitinol) Porcine pericardium Yes Evolut FX Delivery System Transfemoral, direct aortic, subclavian Self expanding 14 equivalent/6 mm (23, 26, 29 mm); 18 equivalent/7.3 mm (34 mm) 108 Indicated for relief of aortic stenosis in patients with symptomatic heart disease due to severe native calcific aortic stenosis who are judged by a heart team, including a cardiac surgeon, to be appropriate for the transcatheter heart valve replacement therapy and for use in patients with symptomatic heart disease due to failure (stenosed, insufficient, or combined) of a surgical bioprosthetic aortic valve who are judged by a heart team, including a cardiac surgeon, to be at high or greater risk for open surgical therapy (ie, STS predicted risk of operative mortality score ≥ 8% or at a ≥ 15% risk of mortality at 30 days) The TAV frame contains embedded gold markers located 3 mm from the inflow and positioned under the commissures
Medtronic Evolut PRO+ Transcatheter Aortic Valve Replacement System 23, 26, 29, 34 45 17/18–30 (CT derived diameters, 17 for TAV-in-SAV only) Nickel titanium (nitinol) Porcine pericardium Yes Evolut Pro+ Delivery System Transfemoral, direct aortic, subclavian Self expanding 14 equivalent/6 mm (23, 26, 29 mm); 18 equivalent/7.3 mm (34 mm) 107 Indicated for relief of aortic stenosis in patients with symptomatic heart disease due to severe native calcific aortic stenosis who are judged by a heart team, including a cardiac surgeon, to be appropriate for the transcatheter heart valve replacement therapy and for use in patients with symptomatic heart disease due to failure (stenosed, insufficient, or combined) of a surgical bioprosthetic aortic valve who are judged by a heart team, including a cardiac surgeon, to be at high or greater risk for open surgical therapy (ie, STS predicted risk of operative mortality score ≥ 8% or at a ≥ 15% risk of mortality at 30 days) –

Valves / Transcatheter Pulmonary Valve Repair

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Company Name Product Name Valve Diameter (mm) Valve Height (mm) Valve Annulus Size Range (mm) Valve Frame Material Valve Leaflet Material Valve Anticalcification Process Delivery System Name Delivery Access Delivery System Deployment Type Delivery System Size (F) Delivery System Working Length (cm) US FDA Indicated Use
Medtronic Harmony Transcatheter Pulmonary Valve 22, 25 51 (25-mm valve diameter), 55 (22-mm valve diameter) Size range determined by perimeter-derived diameter and length of the PA and RVOT Nitinol Porcine pericardium Yes Harmony Delivery Catheter System Venous Self expanding 25, including integrated sheath 100 Indicated for use in the management of pediatric and adult patients with severe pulmonary regurgitation (ie, severe pulmonary regurgitation as determined by echocardiography and/or pulmonary regurgitant fraction ≥ 30% as determined by cardiac MRI) who have a native or surgically repaired right ventricular outflow tract and are clinically indicated for surgical pulmonary valve replacement
Medtronic Melody Transcatheter Pulmonary Valve OD (when expanded to 18, 20, 22): 20.1, 22.4, 24.1 21 at 22-mm ID; 24 at 20-mm ID; 26 at 18-mm ID 18–22 ID Platinum iridium Bovine jugular vein No Ensemble II Transcatheter Delivery System Venous access Balloon-in-balloon expandable 22, including integrated sheath 100 Indicated for use in the management of pediatric and adult patients who have a clinical indication for intervention on a dysfunctional right ventricular outflow tract (RVOT) conduit or surgical bioprosthetic pulmonary valve that has ≥ moderate regurgitation, and/or a mean RVOT gradient ≥ 35 mm Hg

Wires / Diagnostic Wires

View Chart
Company Name Product Name Type (Fixed Core or Movable Core) Diameter (inch) Length (cm) Tip Type Coating Type (Hydrophilic or Hydrophobic) Comments
Medtronic Hi-Torque Flex-T Fixed core 0.018 145, 200, 295 Straight MicroGlide coated Supportive and steerable tapered guidewire
Medtronic Wholey Guide Wire System: Standard Tip, Extension Compatible Fixed core 0.035 145, 175 Modified J/shapeable, straight/shapeable MicroGlide coated Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic Wholey Guide Wire System: Standard Tip, Exchange Length Fixed core 0.035 260, 300 Straight/shapeable MicroGlide coated Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic Wholey Guide Wire System: Modified J Tip, Extension Compatible Fixed core 0.035 145, 175 Straight/shapeable, modified J/shapeable MicroGlide coated Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic Wholey Guide Wire System: Modified J Tip, Exchange Length Fixed core 0.035 260, 300 Modified J/shapeable MicroGlide coated Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic Wholey Guide Wire System: Floppy Tip, Extension Compatible Fixed core 0.035 145, 175 Straight/shapeable MicroGlide coated Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic Wholey Guide Wire System: Floppy Tip, Exchange Length Fixed core 0.035 260, 300 Straight/shapeable MicroGlide coated Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic Wholey Guide Wire System: Extension System Fixed core 0.035 155 Straight/shapeable MicroGlide coated Supportive wire with soft, shapeable tip designed for atraumatic negotiation of the vasculature; core-to-tip design
Medtronic TAD II Fixed core 0.035, tapering to 0.018 145, 200, 260 Straight PTFE coated Supportive and steerable tapered guidewire
Medtronic TAD Fixed core 0.035, tapering to 0.018 145, 200, 300 Straight PTFE coated Supportive and steerable tapered guidewire
Medtronic LOC Extension Fixed core 0.018 115 Straight MicroGlide coated Converts a 145- or 175-cm length to an exchange length ≥ 260 cm

Wires / Interventional Support Wires

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Company Name Product Name Type Diameter (inch) Length (cm) Tip Type Coating Type (Hydrophilic or Hydrophobic) Comments
Medtronic Steerant Super Stiff Guidewire Stainless Steel 0.035 200, 260 Curved, double curve PTFE coating –

Other Devices / Embolic Protection Devices

View Chart
Company Name Product Name Type Position US FDA Indicated Use
Medtronic SpiderFX 3.0–7.0-mm Embolic Protection System Filter Distal Saphenous vein graft and carotid interventions

Other Devices / Snares

View Chart
Company Name Product Name Catheter Size/Length (F/cm) Working Diameters (mm) Snare Length (cm) Snare Type
Medtronic Alligator Retrieval Device Minimum microcatheter size: 0.021-inch ID 2, 3, 4, 5 175 Retrieval device; 0.016-inch guidewire with four platinum jaws
Medtronic Amplatz GooseNeck Microsnare Kit 2.3–3/150 2, 4, 7 175 Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F, 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)
Medtronic Amplatz GooseNeck Microsnare Kit 2.3–3/175 2, 4, 7 200 Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F, 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)
Medtronic Amplatz GooseNeck Snare Kit 4/102 5, 10 120 Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F, 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)
Medtronic Amplatz GooseNeck Snare Kit 6/102 15, 20, 25, 30, 35 120 Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F, 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)
Medtronic Amplatz GooseNeck Snare Kit Petite 4/48, 6/48 10, 25 65 Single 90° loop configuration and gold tungsten coils (for enhanced visualization); replacement catheters available in 4 and 6 F, 6/102, 15, 20, 25, 30, 35 (48- and 102-cm lengths)

Other Devices / Thrombus Aspiration Devices

View Chart
Company Name Product Name Type Maximum Tip Diameter (mm) Minimum Guide Catheter Size (F) Catheter Length (cm)
Medtronic Export Advance Preloaded stylet, full-wall variable hub-to-tip braiding; hydrophilic coating; soft, short tip 1.73 6 140
Medtronic Export AP Catheter Full-wall variable hub-to-tip braiding; hydrophilic coating; short, soft tip 1.73 6 140

Other Devices / Renal Denervation Systems

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Company Name Product Name Modality Recommended Vessel Size (mm) Number of Catheter Sizes Balloon Diameter (mm) Wire Compatibility (inch) Catheter Size (F) Catheter Length (cm) Guide Catheter Compatibility (F) Safety Mechanisms US FDA Indicated Use
Medtronic Symplicity Spyral Radiofrequency Renal arteries 3–8 mm in diameter One – 0.014 4 117 6 Integrated into generator; algorithm to monitor temperature and impedance followed by active power modulation to prevent non-target tissue damage Indicated to reduce blood pressure as an adjunctive treatment in patients with hypertension in whom lifestyle modifications and antihypertensive medications do not adequately control blood pressure

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Coding CTO DES Hypertension Imaging Modalities PCI Pharmacology Radial Regulatory Structural Disease Valvular Interventions
Centers

Coding CTO DES Hypertension Imaging Modalities PCI Pharmacology Radial Regulatory Structural Disease Valvular Interventions

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Cardiac Interventions Today (ISSN 2572-5955 print and ISSN 2572-5963 online) is a publication dedicated to providing coverage of the latest developments in technology, techniques, clinical studies, and regulatory and reimbursement issues in the field of coronary and cardiac interventions.



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