Establishment registration
RUDOLF RIESTER GMBH
FDA establishment registration 8010482 · JUNGINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8010482 |
|---|---|
| Establishment name | RUDOLF RIESTER GMBH |
| Owner/operator | RUDOLF RIESTER GMBH & CO. KG |
| Owner/operator number | 8010492 |
| FEI number | 1000292048 |
| Address | BRUCKSTRASSE 31 |
| City | JUNGINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | CAL, CCW, DQA, DQD, DXN, DXQ, EBA, EPY, EQH, ERA, FSP, FTT, FXF, GAX, GWX, GWZ, HDF, HJH, HKF, HKI, HKM, HKY, HLJ, HRW, KCY, KYT, KZD, KZF, LDE, MWI and 1 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ 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