Establishment registration
AESCULAP AG
FDA establishment registration 9610612 · TUTTLINGEN, DONAU Baden-Wurttemberg, DE
Key facts
| Registration number | 9610612 |
|---|---|
| Establishment name | AESCULAP AG |
| Owner/operator | Aesculap AG |
| Owner/operator number | 8010193 |
| FEI number | 3002806315 |
| Address | AM AESCULAP PLATZ |
| City | TUTTLINGEN, DONAU Baden-Wurttemberg |
| Country | DE |
| Establishment types | Specification developer, Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | BTA, BWN, CCW, DSS, DWH, DWI, DWS, DXC, DXT, DZC, DZM, DZN, EAX, EBR, ECN, ECP, EEF, EFK, EFL, EGN, EHY, EIC, EIF, EIG, EIK, EIR, EIS, EIX, EIY, EJB and 382 more |
| Device classes | 1, 2, 3, U |
At a glance
- 100–999 Device listings
- 1,000+ 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