Establishment registration
KARL STORZ SE & CO. KG
FDA establishment registration 3006546082 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 3006546082 |
|---|---|
| Establishment name | KARL STORZ SE & CO. KG |
| Owner/operator | KARL STORZ SE & CO KG |
| Owner/operator number | 8010119 |
| FEI number | 3006546082 |
| Address | Elsa-Brandstrom-Weg 11-21 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | CAI, CCW, EOB, EOQ, EOX, EPT, EQN, ERA, EWY, EZN, EZO, FAH, FAJ, FAM, FAS, FAX, FBO, FBQ, FCL, FCW, FDC, FDF, FDI, FEC, FEO, FFK, FGA, FGB, FGC, FJL and 32 more |
| Device classes | 1, 2, 3 |
At a glance
- 100–999 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