St. Jude Medical Cardiovascular Division

2 product lines across 2 device categories: Guidewires, Closure devices.

From cardiovascular.abbott, checked October 2026.

Search St. Jude Medical Cardiovascular Division guidewires

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About St. Jude Medical Cardiovascular Division

St. Jude Medical Cardiovascular Division hasn't added a company description yet.

Guidewires

Used in: Uterine Artery Embolization (UAE), Peripheral Balloon Angioplasty, Stroke Thrombectomy, Internal Iliac Artery Embolization

ProductSizes (FDA GUDID)ModelsMRI
HydroSteer
Length: 150–260 cm; Outer Diameter: 0.02–0.04 in28Not stated

Vascular Closure Devices

Used in: Peripheral Balloon Angioplasty, Peripheral Artery Stenting, Endovascular Aneurysm Repair (EVAR), Arterial Access Site Closure (TR Band and Closure Devices)

ProductSizes (FDA GUDID)ModelsMRI
Angio-Seal
Catheter Gauge: 6–8 Fr3MR Safe

Sales representatives

St. Jude Medical Cardiovascular Division has not listed representatives here yet. Contact the company directly:

From cardiovascular.abbott, checked October 2026.

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Frequently asked questions

What devices does St. Jude Medical Cardiovascular Division make?

St. Jude Medical Cardiovascular Division has 2 product lines in our library across 2 device categories: Guidewires, Closure devices.

How do I contact a St. Jude Medical Cardiovascular Division sales representative?

St. Jude Medical Cardiovascular Division has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.

Does LA Vascular sell St. Jude Medical Cardiovascular Division products?

No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact St. Jude Medical Cardiovascular Division or its representatives to buy.

Where do the St. Jude Medical Cardiovascular Division product sizes come from?

From the FDA Global Unique Device Identification Database (GUDID). Confirm sizes and availability with the instructions for use or the manufacturer.

Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.

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