Establishment registration
STORZ AM MARK GMBH
FDA establishment registration 8043554 · EMMINGEN-LIPTINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8043554 |
|---|---|
| Establishment name | STORZ AM MARK GMBH |
| Owner/operator | STORZ AM MARK GMBH |
| Owner/operator number | 9002328 |
| FEI number | 3001000014 |
| Address | EMMINGER STR. 39 |
| City | EMMINGEN-LIPTINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | DZA, DZL, DZN, EAX, ECB, ECR, EEF, EFK, EFL, EGN, EHY, EIF, EIG, EIK, EIL, EIR, EIS, EIX, EIY, EJB, EJG, EJL, EJY, EKB, EKC, EKD, EKE, EKH, EKI, EKJ and 36 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 10–99 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