Establishment registration
GEISTER MEDIZINTECHNIK GMBH
FDA establishment registration 8010697 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8010697 |
|---|---|
| Establishment name | GEISTER MEDIZINTECHNIK GMBH |
| Owner/operator | GEISTER MEDIZINTECHN |
| Owner/operator number | 8010697 |
| FEI number | 3004053982 |
| Address | FOEHRENSTR. 2 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DRC, DTI, DWI, DWP, DWS, DXC, EMD, EML, FFO, FHQ, FSM, GAC, GAD, GCJ, GDG, GDI, GDZ, GEA, GEG, GEN, GES, GEY, GFA, GZT, GZX, HAE, HAO, HBT, HCZ, HGC and 19 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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