FDA device listing
Hypodermic Needle for Single Use,K-Pack Surshield Needle,
FDA device listing 1845967739 · Terumo Europe N.V.
Key facts
| Proprietary names | Hypodermic Needle for Single Use,K-Pack Surshield Needle, |
|---|---|
| Owner/operator | Terumo Europe N.V. |
| Owner/operator number | 10034088 |
| Premarket submissions | K110527 |
| 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 | TERUMO EUROPE N.V. |
| Establishment registrations | 9681413 |
| FEI numbers | 3001570557 |
| 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