Establishment registration
Harps Europe Manufacturing
FDA establishment registration 3007478974 · WIMPASSING NIEDEROSTERREICH, AT
Key facts
| Registration number | 3007478974 |
|---|---|
| Establishment name | Harps Europe Manufacturing |
| Owner/operator | Harps Europe Manufacturing |
| Owner/operator number | 8020005 |
| FEI number | 3007478974 |
| Address | TRIESTER BUNDESSTRASSE 26 |
| City | WIMPASSING NIEDEROSTERREICH |
| Country | AT |
| Registration valid through | 2026 |
| Product codes listed | KGO, LZC |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- 100–999 UDI devices (GUDID)
- Current Registration current
- 1–9 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