Establishment registration
WEINMANN GMBH CHIRURGISCHE INSTRUMENTE
FDA establishment registration 9611815 · SEITINGEN-OBERFLACHT Baden-Wurttemberg, DE
Key facts
| Registration number | 9611815 |
|---|---|
| Establishment name | WEINMANN GMBH CHIRURGISCHE INSTRUMENTE |
| Owner/operator | WEINMANN GMBH CHIRURGISCHE INSTRUMENTE |
| Owner/operator number | 8010280 |
| FEI number | 3002808483 |
| Address | Hohnerstr. 31 |
| City | SEITINGEN-OBERFLACHT Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | GDO, HAO, HFB, HTX, LRY, LXH |
| Device classes | 1 |
At a glance
- 1–9 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