Closure devices
StarClose SE
A non-bioabsorbable metallic clip intended to be implanted following a percutaneous catheterization procedure to close the punctured access site on an artery (typically femoral) and improve haemostasis. It is typically a small circular clip with grasping blades intended to close inwardly upon deployment; dedicated disposable devices (e.g., applicator) intended for implantation may be included with the device.
StarClose SE models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 14679-01 | — | MR Conditional | Available |
| 14679-05 | — | MR Conditional | Available |
Procedures that use closure devices
Frequently asked questions
What is StarClose SE used for?
A non-bioabsorbable metallic clip intended to be implanted following a percutaneous catheterization procedure to close the punctured access site on an artery (typically femoral) and improve haemostasis. It is typically a small circular clip with grasping blades intended to close inwardly upon deployment; dedicated disposable devices (e.g., applicator) intended for implantation may be included with the device.
Who makes StarClose SE?
StarClose SE is made by Abbott Vascular Inc.. It is listed under vascular closure devices in our device library.
What sizes does StarClose SE come in?
The FDA device database does not list sizes for StarClose SE. Check the instructions for use or ask a Abbott Vascular Inc. representative.
Is StarClose SE MRI safe?
The FDA device database lists StarClose SE as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is StarClose SE FDA cleared?
StarClose SE is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Abbott Vascular Inc. sales representative?
Abbott Vascular Inc. has not listed representatives on LA Vascular yet. Visit the Abbott Vascular Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.