HSK-3038: Maquet Heartstring III Proximal Seal System: 3.8mm

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| Price: | $15.00 per box of 1 |
|---|---|
| Quantity: | |
| In Stock: | 25 box of 1 |
| Status: | expired |
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Additional Details
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.
AccessGUDID Info
- 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.
Manufacturer
Maquet, a key part of the Getinge Group, is a global leader in providing advanced medical technology and solutions for critical care, operating rooms, and cardiovascular procedures. Headquartered in Gothenburg, Sweden, Maquet specializes in a wide range of products, including surgical tables, lights, anesthesia systems, heart-lung machines, and extracorporeal life support (ECLS) systems. Renowned for its focus on innovation, quality, and patient safety, Maquet collaborates closely with healthcare professionals to develop solutions that improve outcomes and enhance clinical efficiency. As a cornerstone of Getinge’s mission, Maquet drives advancements in healthcare through its dedication to life-saving technologies and superior support.
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