FDA device listing
NovoFine® Plus,NovoFine® Plus 32G 4 mm
FDA device listing 1382197461 · NOVO NORDISK INC.
Key facts
| Proprietary names | NovoFine® Plus,NovoFine® Plus 32G 4 mm |
|---|---|
| Owner/operator | NOVO NORDISK INC. |
| Owner/operator number | 9027307 |
| Premarket submissions | K202005 |
| Product codes | FMI |
| Device names | FMI - Needle, Hypodermic, Single Lumen |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5570 |
| Review panels | General Hospital |
| Registered establishments | NOVO NORDISK A/S, NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI, NOVO NORDISK INC. |
| Establishment registrations | 2244771, 9681821, 9681822 |
| FEI numbers | 2244771, 3003131673, 3004547341 |
| Establishment operations | Complaint File Establishment, Manufacturer, Specification Developer |
| 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