Vasorum Limited
5 product lines across 1 device categories: Closure devices.
From vasorum.ie, checked November 2026.
About Vasorum Limited
Vasorum Limited hasn't added a company description yet.
Vascular Closure Devices
Used in: Peripheral Balloon Angioplasty, Peripheral Artery Stenting, Endovascular Aneurysm Repair (EVAR), Arterial Access Site Closure (TR Band and Closure Devices)
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Celt ACD PLUS Vascular Closure Device 7F Celt ACD PLUS Vascular Closure Device 7F (US) | Catheter Gauge: 5–7 Fr | 3 | MR Conditional |
| Celt ACD Vascular Closure Device 6F | Catheter Gauge: 6–7 Fr | 2 | MR Conditional |
| Celt ACD Vascular Closure Device 7F_ESP | Catheter Gauge: 7 Fr | 1 | MR Conditional |
| Celt ACD Vascular Closure Device 5F_ESP | Catheter Gauge: 5 Fr | 1 | MR Conditional |
| Celt ACD Vascular Closure Device 6F_ESP | Catheter Gauge: 6 Fr | 1 | MR Conditional |
Sales representatives
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From vasorum.ie, checked November 2026.
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FDA clearances and approvals
- celt acd vascular closure device PMA P150006, 2017
Frequently asked questions
What devices does Vasorum Limited make?
Vasorum Limited has 5 product lines in our library across 1 device category: Closure devices.
Are Vasorum Limited devices FDA cleared?
Our library lists FDA clearances and approvals for Vasorum Limited products. The most recent is celt acd vascular closure device (PMA P150006, 2017).
How do I contact a Vasorum Limited sales representative?
Vasorum Limited has not listed sales representatives on LA Vascular yet. Use the company contact details on this page.
Does LA Vascular sell Vasorum Limited products?
No. LA Vascular is an educational reference. We do not sell devices or quote device prices; contact Vasorum Limited or its representatives to buy.
Where do the Vasorum Limited product sizes come from?
From the FDA Global Unique Device Identification Database (GUDID). Confirm sizes and availability with the instructions for use or the manufacturer.
Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.