HSK-3043

Maquet Heartstring III Proximal Seal System: 4.3mm

$15.00 box of 1

In Stock: 11 Eaches

Expiration: Expired

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The item listed above is expired and may be used for educational, training, and non-clinical research purposes only. Any product information appearing below, including the product indication statement, pertains to an in-date item only.

Description

Maquet Getinge HEARTSTRING® III PROXIMAL SEAL SYSTEM

The HEARTSTRING Proximal Seal System allows you to achieve clampless hemostasis during CABG proximal anastomoses while suturing with your own hand. It's an easy-to-use advance in patient care and helps reduce the release of emboli that can potentially have post-surgical neurocognitive consequences for patients.

Sterilization

  • Device Packaged as Sterile: Yes
  • Requires Sterilization Prior to Use: No 

Additional Details

  • Company Name: Getinge Maquet Cardiovascular, LLC
  • FDA Product Code: DXC
  • FDA Product Code Name: Clamp, Vascular 
  • GMDN Term Code: 47110
  • GMDN Term Name: Intravascular anastomosis occluder
  • GMDN Term Definition: A device designed to temporarily occlude the flow of blood in the lumen of a blood vessel at a vascular anastomosis, primarily to control bleeding and enable operative field visualization during coronary or peripheral vascular bypass grafting and vessel repair surgery. It is typically designed as a flexible shaft with dilated/bulbous ends that is entirely inserted into the vessel lumen via a small incision at the surgical site to arrest blood flow at the anastomosis; it will typically have an external tab or tether used for its removal. It is typically made of silicone elastomer and polyester radiopaque materials and is available in a range of diameters. This is a single-use device.

Additional information

Size

1

Arms

N/A

Manufacturer

Unit

box of 1

  • FDA Product Code: DXC
  • FDA Product Code Name: Clamp, Vascular
  • GMDN Term Code: 47110
  • GMDN Term Name: Intravascular anastomosis occluder
  • GMDN Term Description: A device designed to temporarily occlude the flow of blood in the lumen of a blood vessel at a vascular anastomosis, primarily to control bleeding and enable operative field visualization during coronary or peripheral vascular bypass grafting and vessel repair surgery. It is typically designed as a flexible shaft with dilated/bulbous ends that is entirely inserted into the vessel lumen via a small incision at the surgical site to arrest blood flow at the anastomosis; it will typically have an external tab or tether used for its removal. It is typically made of silicone elastomer and polyester radiopaque materials and is available in a range of diameters. This is a single-use device.

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