Establishment registration
MEDART TECHNOLOGY EUROPE
FDA establishment registration 3038189188 · Annecy Savoie, FR
Key facts
| Registration number | 3038189188 |
|---|---|
| Establishment name | MEDART TECHNOLOGY EUROPE |
| Owner/operator | MedArt Technology Europe |
| Owner/operator number | 10093012 |
| FEI number | 3038189188 |
| Address | 324 Route des Vernes 74370 Annecy , France |
| City | Annecy Savoie |
| Country | FR |
| Registration valid through | 2026 |
| Product codes listed | GEX, NGX |
| 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