Establishment registration
NEUROMOD DEVICES LIMITED
FDA establishment registration 3018030059 · Dublin Dublin(City), IE
Key facts
| Registration number | 3018030059 |
|---|---|
| Establishment name | NEUROMOD DEVICES LIMITED |
| Owner/operator | Neuromod Devices Limited |
| Owner/operator number | 10087563 |
| FEI number | 3018030059 |
| Address | Rainsford Street |
| City | Dublin Dublin(City) |
| Country | IE |
| Establishment types | Specification developer, Repackager/relabeler, Complaint file establishment |
| Registration valid through | 2026 |
| Product codes listed | QVN |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database