Establishment registration
PRO-MED INSTRUMENTE GMBH
FDA establishment registration 8010733 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 8010733 |
|---|---|
| Establishment name | PRO-MED INSTRUMENTE GMBH |
| Owner/operator | PRO-MED Instrumente GmbH |
| Owner/operator number | 8010733 |
| FEI number | 3001417518 |
| Address | 9 GAENSAECKER |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | ECB, EFL, EML, FFO, FSM, FTY, FZO, GDG, GFJ, HNR, HRQ, HTD, HTF, HTS, HTT, HTX, HTZ, HXB, HXK, HXW, HXX, HXZ, HYA, JZF, KAD, KAL, KBW, KCB, KDG, KIK and 3 more |
| Device classes | 1 |
At a glance
- 10–99 Device listings
- None 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