Establishment registration
MAX HAUSER SUDDEUTSCHE CHIRURGIEMECHANIK GMBH
FDA establishment registration 8010422 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8010422 |
|---|---|
| Establishment name | MAX HAUSER SUDDEUTSCHE CHIRURGIEMECHANIK GMBH |
| Owner/operator | MAX HAUSER SUDDEUTSCHE CHIRURGIEMECHANIK GMBH |
| Owner/operator number | 8010422 |
| FEI number | 3008238512 |
| Address | Im Mittleren Oesch 4 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DWS, DXC, DZN, EFL, EIG, FFN, FFO, FGN, FHQ, GAD, GCJ, GDJ, GEJ, GEN, GZT, HAE, HAO, HDL, HGC, HGE, HRQ, HRR, HTD, HTX, HTZ, HXD, HXK, JYG, JYR, KAE and 6 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