Establishment registration
3D-SIDE
FDA establishment registration 3013561205 · Mont Saint Guibert Brabant Wallon, BE
Key facts
| Registration number | 3013561205 |
|---|---|
| Establishment name | 3D-SIDE |
| Owner/operator | 3D-Side |
| Owner/operator number | 10054501 |
| FEI number | 3013561205 |
| Address | Rue Dumont, 5 |
| City | Mont Saint Guibert Brabant Wallon |
| Country | BE |
| Registration valid through | 2026 |
| Product codes listed | HRS, HWC, KWS, PBF, PHX, QHE, QIH |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 10–99 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