Closure devices
Cordis ExoSeal Vascular Closure Device
An implantable, bioabsorbable device designed for haemostasis/closure of a femoral artery access (catheterization) site, through pressure/compression, as an alternative to manual compression or surgical techniques to reduce the time to haemostasis; it may additionally be intended for femoral vein access site closure. It consists of a bioabsorbable synthetic polymer plug and/or patch [e.g., polyglycolic acid (PGA)] that is implanted onto the extravascular (plug-like) and/or intravascular (patch-like) surface of the femoral artery access site. Delivery device(s) dedicated to plug/patch introduction are typically included with the plug/patch.
Procedures that use closure devices
Frequently asked questions
What is Cordis ExoSeal Vascular Closure Device used for?
An implantable, bioabsorbable device designed for haemostasis/closure of a femoral artery access (catheterization) site, through pressure/compression, as an alternative to manual compression or surgical techniques to reduce the time to haemostasis; it may additionally be intended for femoral vein access site closure. It consists of a bioabsorbable synthetic polymer plug and/or patch [e.g., polyglycolic acid (PGA)] that is implanted onto the extravascular (plug-like) and/or intravascular (patch-like) surface of the femoral artery access site. Delivery device(s) dedicated to plug/patch introduction are typically included with the plug/patch.
Who makes Cordis ExoSeal Vascular Closure Device?
Cordis ExoSeal Vascular Closure Device is made by Cordis US Corp.. It is listed under vascular closure devices in our device library.
What sizes does Cordis ExoSeal Vascular Closure Device come in?
The FDA device database does not list sizes for Cordis ExoSeal Vascular Closure Device. Check the instructions for use or ask a Cordis US Corp. representative.
Is Cordis ExoSeal Vascular Closure Device MRI safe?
The FDA device database lists Cordis ExoSeal Vascular Closure Device as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Cordis ExoSeal Vascular Closure Device FDA cleared?
Cordis ExoSeal Vascular Closure Device is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Cordis US Corp. sales representative?
Cordis US Corp. has not listed representatives on LA Vascular yet. Visit the Cordis US Corp. 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.