FDA device listing
Omnifix Syringe NRFit
FDA device listing 1386400848 · B. BRAUN MELSUNGEN AG
Key facts
| Proprietary names | Omnifix Syringe NRFit |
|---|---|
| Owner/operator | B. BRAUN MELSUNGEN AG |
| Owner/operator number | 8010484 |
| Premarket submissions | K241385 |
| Product codes | FMF, QEH |
| Device names | FMF - Syringe, Piston, QEH - Piston Syringe With Neuraxial Connector – Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5860 |
| Review panels | General Hospital |
| Registered establishments | B. BRAUN MEDICAL AG, B. BRAUN MELSUNGEN AG |
| Establishment registrations | 8031007, 9610825 |
| FEI numbers | 5637, 3002806469 |
| Establishment operations | Contract Manufacturer, Foreign Exporter, Specification Developer |
| 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