FDA device listing
Anti-Reflux Filter,Nasogastric Sump Tube with PreVent
FDA device listing 2035947347 · C. R. Bard, Inc.
Key facts
| Proprietary names | Anti-Reflux Filter,Nasogastric Sump Tube with PreVent |
|---|---|
| Owner/operator | C. R. Bard, Inc. |
| Owner/operator number | 2212754 |
| Premarket submissions | K960176 |
| Product codes | FEG |
| Device names | FEG - Tube, Double Lumen For Intestinal Decompression And/Or Intubation |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.5980 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | C.R. BARD, INC., PRODUCTOS PARA EL CUIDADO DE LA SALUD |
| Establishment registrations | 1018233, 9611590, 3006082230 |
| FEI numbers | 1018233, 1000237915, 3006082230 |
| Establishment operations | Contract Manufacturer, Contract Sterilizer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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