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Less trauma,
faster procedures

Through low profile
(5FR compatibility for all sizes)

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Outstanding lesion access

Through exceptional flexibility

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Cost effective

Through 3-years shelf life

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The BeGraft Coronary Stent Graft System is indicated for the treatment of acute coronary artery perforation
and rupture, coronary artery aneurysm and coronary bypass-vein graft aneurysm.

The BeGraft Coronary Stent Graft System is not available in the US.

Compliance chart
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MRI statements

Non-clinical testing has demonstrated that the “BeGraft Coronary Stent Graft” is MR Conditional. A patient with this device can be safely scanned immediately after implantation in an MR system meeting the following conditions:

  • static magnetic field of 1.5 Tesla and 3 Tesla, with
  • maximum spatial field gradient of 6,500 G/cm (65 T/m)
  • maximum force product of 117,000,000 G²/cm (117 T²/m)
  • theoretically estimated maximum whole body averaged (WBA) specific absorption rate (SAR) of 2 W/kg (normal operating mode)

Under the scan conditions defined above, the “BeGraft Coronary Stent Graft” is expected to produce a maximum temperature rise of less than

  • 2.0°C (2 W/kg, 1.5 Tesla) RF-related temperature increase with a background temperature increase of ≈ 1.6°C (2 W/kg, 1.5 Tesla)
  • 1.4°C (2 W/kg, 3 Tesla) RF-related temperature increase with a background temperature increase of ≈ 1.0°C (2 W/kg, 3 Tesla)

after 15 minutes of continuous scanning.

The effect of heating in the MRI environment for overlapping stent grafts or stent grafts with fractured struts is not known. In non-clinical testing, the image artifact caused by the device extends approximately 8.93 mm from the “BeGraft Coronary Stent Graft” when imaged with a spin echo pulse sequence and a 3 Tesla MR system.

For further information, please see the current version of the IFUs.