ProPlege peripheral retrograde cardioplegia device

The ProPlege peripheral retrograde cardioplegia device is indicated for occlusion of the coronary sinus, delivery of cardioplegia solution, and monitoring of coronary sinus pressure during cardiopulmonary bypass.

  • 9 Fr (3.1 mm), 59 cm long, triple-lumen, articulating device
  • Designed for occluding the coronary sinus for retrograde perfusion of the coronary circulation
  • Balloon expands to occlude a range of coronary sinus diameters
  • Delivers cardioplegia solution to the coronary sinus
  • Allows coronary sinus pressure monitoring distal to the balloon
  • An articulation mechanism allows for changes to the curvature of the distal end of the device
  • Provided with a contamination guard, which connects to the introducer sheath

Contents:

  • 1 ProPlege peripheral retrograde cardioplegia device
  • 1 Syringe (30 ml), for flushing and priming the ProPlege device
  • 1 Syringe (3 ml), for balloon inflation and deflation
  • Introducer sheath kit
    • – 1 Introducer 11 Fr (3.7 mm)
    • – 1 J-tip guidewire
    • – 1 18 gauge introducer needle

ProPlege device

Articulating positions

Diameter vs volume

ProPlege Device
Articulating-Positions
Diameter vs Volume
ProPlege Device

Articulating positions

Articulating-Positions

Diameter vs volume

Diameter vs Volume

ProPlege peripheral retrograde cardioplegia device

Instructions for product preparation

ProPlege device brochure

Necklines: Placing the ProPlege device and EndoVent catheter

David M. Stout, M.D.
Chief of Cardiovascular Anesthesiology
Swedish Heart and Vascular Institute, Seattle, Washington

Coronary sinus catheter placement whitepaper

ThruPort ProPlege device training presentation

ModelDescriptionSizeImage
PR9 ProPlege peripheral retrograde cardioplegia device 9 Fr

Contact a sales representative

Important safety information

Caution: Federal (United States) law restricts this device to sale by or on the order of a physician.
See Instructions For Use (IFU) / Directions For Use (DFU) for full prescribing information, including indications, contraindications, warnings, precautions and adverse events.

Important safety information

Caution: Federal (United States) law restricts this device to sale by or on the order of a physician.
See Instructions For Use (IFU) / Directions For Use (DFU) for full prescribing information, including indications, contraindications, warnings, precautions and adverse events.

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