FDA device listing
LifeStent 5F Vascular Stent System,Lifestent and Lifestent XL Vascular Stent System,Lifestent Solo Vascular Stent System
FDA device listing 1319940737 · C. R. Bard, Inc.
Key facts
| Proprietary names | LifeStent 5F Vascular Stent System,Lifestent and Lifestent XL Vascular Stent System,Lifestent Solo Vascular Stent System |
|---|---|
| Owner/operator | C. R. Bard, Inc. |
| Owner/operator number | 2212754 |
| Premarket submissions | P070014 |
| Product codes | NIP |
| Device names | NIP - Stent, Superficial Femoral Artery |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.NIP |
| Review panels | Cardiovascular |
| Registered establishments | ANGIOMED GMBH & CO. MEDIZINTECHNIK KG, Bard European Distribution Center NV, BARD PERIPHERAL VASCULAR, INC. |
| Establishment registrations | 2020394, 9681442, 3002504068 |
| FEI numbers | 2020394, 3002504068, 3002806368 |
| Establishment operations | Complaint File Establishment, Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database