FDA device listing
ECLIPSE Ci-E,ECLIPSE Ci-L,ECLIPSE Ci-L plus,ECLIPSE Ci-S,ECLIPSE Ei L,ECLIPSE Ei R,ECLIPSE Ni-E,ECLIPSE Ni-L,ECLIPSE…
FDA device listing 2005249078 · NIKON CORPORATION
Key facts
| Proprietary names | ECLIPSE Ci-E,ECLIPSE Ci-L,ECLIPSE Ci-L plus,ECLIPSE Ci-S,ECLIPSE Ei L,ECLIPSE Ei R,ECLIPSE Ni-E,ECLIPSE Ni-L,ECLIPSE Ni-U,ECLIPSE Si RS,ECLIPSE Ti2-A,ECLIPSE Ti2-E,ECLIPSE Ti2-E/B,ECLIPSE Ti2-U,ECLIPSE Ts2,ECLIPSE Ts2-FL,ECLIPSE Ts2R,ECLIPSE Ts2R-FL,ECLIPSE Ui US,SMZ1270,SMZ1270i,SMZ18,SMZ25,SMZ800N |
|---|---|
| Owner/operator | NIKON CORPORATION |
| Owner/operator number | 10044219 |
| Product codes | IBJ |
| Device names | IBJ - Light, Microscope |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.3600 |
| Review panels | Pathology |
| Registered establishments | NIKON CORPORATION |
| Establishment registrations | 3001111904 |
| FEI numbers | 3001111904 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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