Establishment registration
CARL TEUFEL GMBH & CO. KG
FDA establishment registration 9611502 · LIPTINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9611502 |
|---|---|
| Establishment name | CARL TEUFEL GMBH & CO. KG |
| Owner/operator | SCHWEIZER GMBH |
| Owner/operator number | 8010367 |
| FEI number | 3002806755 |
| Address | TUTTLINGER ST. 30 |
| City | LIPTINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DWS, EGN, EIR, FHQ, FTY, FZT, GZX, HAO, HDK, HMR, HMX, HNA, HNB, HNC, HND, HNF, HNH, HNJ, HNN, HNQ, HNR, HNZ, HOB, HOD, HOE, HPN, HRR, HXB, HXK, JYA and 6 more |
| Device classes | 1 |
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