Establishment registration
OERTEL MEDICAL GMBH
FDA establishment registration 9612075 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9612075 |
|---|---|
| Establishment name | OERTEL MEDICAL GMBH |
| Owner/operator | OERTEL MEDICAL GMBH |
| Owner/operator number | 8010226 |
| FEI number | 3002809480 |
| Address | OBERE VORSTADT 19-20 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | EIG, EJB, EMI, EMJ, EMM, FHB, FZO, GAC, GAD, GDG, GDI, GDZ, GEG, GEO, HAO, HDE, HLN, HMQ, HMR, HMX, HNB, HND, HNH, HNI, HNL, HNN, HNQ, HNW, HNX, HNZ and 25 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