FDA device listing
SELECT
FDA device listing 1119923243 · Medtronic, Inc.
Key facts
| Proprietary names | SELECT |
|---|---|
| Owner/operator | Medtronic, Inc. |
| Owner/operator number | 2112641 |
| Premarket submissions | K840002 |
| 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 | Medtronic Distribution Center, Medtronic Grand Rapids, Medtronic Mexico S. de R.L. de CV, MEDTRONIC PERFUSION SYSTEMS |
| Establishment registrations | 2184009, 9617601, 3003955307, 3009380063 |
| FEI numbers | 1000116158, 3002534070, 3003955307, 3009380063 |
| Establishment operations | Manufacturer, Repackager/Relabeler, Specification Developer |
| 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