Establishment registration
RUDOLF MEDICAL GMBH + CO. KG
FDA establishment registration 8010298 · FRIDINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8010298 |
|---|---|
| Establishment name | RUDOLF MEDICAL GMBH + CO. KG |
| Owner/operator | RUDOLF MEDICAL GMBH + CO. KG |
| Owner/operator number | 8010298 |
| FEI number | 3003448211 |
| Address | ZOLLERSTRASSE 1 |
| City | FRIDINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | CCW, DWS, EBA, EFL, EMF, EPY, ERA, FAJ, FAX, FBM, FCL, FET, FFO, FFQ, FGB, FHL, FHQ, FSM, FZO, FZQ, FZS, FZT, FZX, GAD, GAF, GAI, GBZ, GCJ, GCT, GDF and 64 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- None 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