Establishment registration
SUTTER MEDIZINTECHNIK GMBH
FDA establishment registration 8044091 · Emmendingen Baden-Wurttemberg, DE
Key facts
| Registration number | 8044091 |
|---|---|
| Establishment name | SUTTER MEDIZINTECHNIK GMBH |
| Owner/operator | Sutter Medizintechnik GmbH |
| Owner/operator number | 9005453 |
| FEI number | 3004857377 |
| Address | Alfred-Walz-Strasse 22 |
| City | Emmendingen Baden-Wurttemberg |
| Country | DE |
| Establishment types | Specification developer, Complaint file establishment, Foreign exporter |
| Registration valid through | 2026 |
| Product codes listed | EOB, FQH, FSM, GEI, HRX |
| 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