Establishment registration
ACKERMANN INSTRUMENTE GMBH
FDA establishment registration 8010273 · RIETHEIM, WEILHEIM Baden-Wurttemberg, DE
Key facts
| Registration number | 8010273 |
|---|---|
| Establishment name | ACKERMANN INSTRUMENTE GMBH |
| Owner/operator | ACKERMANN INSTRUMENTE GMBH |
| Owner/operator number | 8010273 |
| FEI number | 4486 |
| Address | EISENBAHNSTR. 65-67 |
| City | RIETHEIM, WEILHEIM Baden-Wurttemberg |
| Country | DE |
| Establishment types | Repackager/relabeler, Foreign private label distributor |
| Registration valid through | 2026 |
| Product codes listed | BWN, CCX, DWS, EMF, EOQ, EPY, ERA, EZO, FFO, FGO, FGY, FLG, FSM, FTX, FWF, FXE, FZP, FZS, GAD, GCJ, GCX, GDF, GDI, GDJ, GDO, GDZ, GEA, GEI, GEN, GZX and 28 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ 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