FDA device listing
R501-R502 aortic root cannulae
FDA device listing 1647989166 · SORIN GROUP ITALIA S.R.L
Key facts
| Proprietary names | R501-R502 aortic root cannulae |
|---|---|
| Owner/operator | SORIN GROUP ITALIA S.R.L |
| Owner/operator number | 9011842 |
| Premarket submissions | K240193 |
| Product codes | DWF |
| Device names | DWF - Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.4210 |
| Review panels | Cardiovascular |
| Registered establishments | SORIN GROUP ITALIA S.R.L |
| Establishment registrations | 9680841 |
| FEI numbers | 3005426550 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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