Establishment registration
ARVATO Netherlands B.V.
FDA establishment registration 3013302242 · Heijen Limburg, NL
Key facts
| Registration number | 3013302242 |
|---|---|
| Establishment name | ARVATO Netherlands B.V. |
| Owner/operator | Arvato Netherlands B.V. |
| Owner/operator number | 10077655 |
| FEI number | 3013302242 |
| Address | Brem 1 |
| City | Heijen Limburg |
| Country | NL |
| Registration valid through | 2026 |
| Product codes listed | FSM, FZX, GAT, GEI, GXI, HAW, HRS, HSB, HSD, HSX, HTW, HTY, HWC, JDG, JDI, JDJ, JDQ, JDS, JWH, KRR, KTT, KWL, KWS, KWY, KWZ, LPH, LWJ, LZO, LZY, MBI and 6 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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