Establishment registration
CARL ZEISS MEDITEC AG (Munich)
FDA establishment registration 3009746052 · Muenchen Bavaria, DE
Key facts
| Registration number | 3009746052 |
|---|---|
| Establishment name | CARL ZEISS MEDITEC AG (Munich) |
| Owner/operator | Carl Zeiss Meditec AG (Jena) |
| Owner/operator number | 9053564 |
| FEI number | 3009746052 |
| Address | Kistlerhof Strasse 75 |
| City | Muenchen Bavaria |
| Country | DE |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | EPT, HJO, HKI, HMR, HRM, LMD, NFG, NFJ, OBO |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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