Establishment registration
HERMANN MUELLER Medizintechnik GmbH
FDA establishment registration 9680735 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9680735 |
|---|---|
| Establishment name | HERMANN MUELLER Medizintechnik GmbH |
| Owner/operator | Hermann Mueller Medizintechnik GmbH |
| Owner/operator number | 9010992 |
| FEI number | 3004095748 |
| Address | DR. KARL-STORZ-STR. 3 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Repackager/relabeler, Foreign exporter |
| Registration valid through | 2026 |
| Product codes listed | EIG, EIK, EIY, EKB, EKC, EKR, EMF, EMI, EMJ, EMM, EPY, FFO, FTY, FZO, FZR, FZS, FZX, GAC, GAD, GDG, GDO, GDX, GEG, HDF, HRT, HTP, HWM, HXB, HXG, KBM and 3 more |
| 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