Establishment registration
Arthrex Distribution Hub EMEA B.V.
FDA establishment registration 3016851379 · Venlo Limburg, NL
Key facts
| Registration number | 3016851379 |
|---|---|
| Establishment name | Arthrex Distribution Hub EMEA B.V. |
| Owner/operator | ARTHREX, INC. |
| Owner/operator number | 1220287 |
| FEI number | 3016851379 |
| Address | Amperestraat 9 |
| City | Venlo Limburg |
| Country | NL |
| Registration valid through | 2026 |
| Product codes listed | BWN, BZN, DXJ, FEI, FLE, FMF, FRG, FRO, FSM, FWB, FWL, FWZ, FZW, GAB, GAP, GAS, GAT, GAZ, GCJ, GEI, GFA, GFF, HAB, HRS, HRX, HSB, HSD, HST, HSX, HTD and 53 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 Device listings
- 1,000+ 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