Establishment registration
STERIS Deutschland GmBh
FDA establishment registration 3006554912 · Wurmlingen Baden-Wurttemberg, DE
Key facts
| Registration number | 3006554912 |
|---|---|
| Establishment name | STERIS Deutschland GmBh |
| Owner/operator | STERIS |
| Owner/operator number | 10091086 |
| FEI number | 3006554912 |
| Address | KANTSTRASSE 33/1 |
| City | Wurmlingen Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | BWB, CCQ, DRC, DWO, DWS, DXC, EFL, EMF, EMI, EMK, EMM, EPY, EXX, EZO, FAJ, FBM, FBX, FCL, FER, FFN, FFO, FFQ, FFR, FGM, FGN, FHA, FHB, FHL, FHN, FHQ and 132 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- None 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