Establishment registration
RUDOLF STORZ GMBH
FDA establishment registration 9611274 · EMMINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9611274 |
|---|---|
| Establishment name | RUDOLF STORZ GMBH |
| Owner/operator | RUDOLF STORZ GMBH |
| Owner/operator number | 8010286 |
| FEI number | 3002808043 |
| Address | FRIEDRICH-WOEHLER-STR. 13 |
| City | EMMINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DWS, EBL, EIL, EKE, EMF, EMH, EMI, EML, EXX, EYR, FCW, FFO, FFQ, FFY, FHL, FMA, FMP, FSM, FTY, FZO, FZR, FZS, FZX, FZY, GAC, GAD, GAF, GCJ, GCY, GDG and 71 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 1–9 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