Cardiva Medical, Inc.
7 product lines across 2 device categories: TR bands, Closure devices.
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Radial Compression Devices (TR Band)
Used in: Arterial Access Site Closure (TR Band and Closure Devices)
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Cardiva Catalyst II VCS The Cardiva Catalyst™ II consists of a sterile disposable Catalyst II Wire and a sterile disposable Catalyst Clip. The Cardiva Catalyst II… | Catheter Gauge: 5–7 Fr | 1 | Not stated |
| Cardiva Catalyst III VCS The Cardiva Catalyst III consists of a sterile disposable Catalyst III Wire and a sterile disposable Catalyst Clip. The Cardiva Catalyst III… | Catheter Gauge: 5–7 Fr | 1 | Not stated |
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 |
|---|---|---|---|
| Cardiva VASCADE MVP VVCS 6-12F The VASCADE MVP Venous Vascular Closure System (VVCS) is intended to seal femoral veins with single or multiple access sites in one… | — | 1 | MR Safe |
| Cardiva VASCADE MVP XL VVCS 10-12F The VASCADE MVP XL Venous Vascular Closure System (VVCS) 10-12F is intended to seal femoral veins with single or multiple access sites… | — | 1 | MR Safe |
| Cardiva VASCADE 5F VCS The VASCADE VCS is intended to seal femoral vessel puncture sites at the completion of catheter-based procedures. The system is designed to… | Catheter Gauge: 5 Fr | 1 | MR Safe |
| Cardiva VASCADE 6/7F VCS The VASCADE VCS is intended to seal femoral vessel puncture sites at the completion of catheter-based procedures. The system is designed to… | Catheter Gauge: 6–7 Fr | 1 | MR Safe |
| VASCADE MVP XL VVCS The VASCADE MVP XL Venous Vascular Closure System (VVCS) is intended to seal femoral veins with single or multiple access sites in… | — | 1 | MR Safe |
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FDA clearances and approvals
- cardiva vascade vascular closure system vcs PMA P120016, 2019
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.