Closure devices
Celt ACD Vascular Closure Device 5F_ESP
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.
Celt ACD Vascular Closure Device 5F_ESP 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 |
|---|---|---|---|
| KCLT-05 | Catheter Gauge 5 Fr | MR Conditional | Available |
FDA clearances
- PMA P150006 June 2017
Procedures that use closure devices
Frequently asked questions
What is Celt ACD Vascular Closure Device 5F_ESP 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 Celt ACD Vascular Closure Device 5F_ESP?
Celt ACD Vascular Closure Device 5F_ESP is made by Vasorum Limited. It is listed under vascular closure devices in our device library.
What sizes does Celt ACD Vascular Closure Device 5F_ESP come in?
Sizes listed for Celt ACD Vascular Closure Device 5F_ESP: Catheter Gauge: 5 Fr. Confirm availability with the manufacturer's instructions for use.
Is Celt ACD Vascular Closure Device 5F_ESP MRI safe?
The FDA device database lists Celt ACD Vascular Closure Device 5F_ESP as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Celt ACD Vascular Closure Device 5F_ESP FDA cleared?
Celt ACD Vascular Closure Device 5F_ESP is covered by FDA submission P150006.
How do I contact a Vasorum Limited sales representative?
Vasorum Limited has not listed representatives on LA Vascular yet. Visit the Vasorum Limited 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.