Establishment registration
AESCULAP CHIFA SP. Z O.O.
FDA establishment registration 9680260 · NOWY TOMYSL Wielkopolskie, PL
Key facts
| Registration number | 9680260 |
|---|---|
| Establishment name | AESCULAP CHIFA SP. Z O.O. |
| Owner/operator | AESCULAP CHIFA SP. Z O. O. |
| Owner/operator number | 9007699 |
| FEI number | 3002315844 |
| Address | UL. TYSIACLECIA 14 |
| City | NOWY TOMYSL Wielkopolskie |
| Country | PL |
| Registration valid through | 2026 |
| Product codes listed | DYG, ECP, EGN, EIR, EJG, EJY, EMG, EMH, EMJ, FFO, FHQ, FSM, FZS, FZT, GAD, GCX, GDH, GDJ, GDZ, GEG, GEI, GEJ, GEN, GEO, GFJ, GXN, GXQ, GZX, HAE, HCI and 12 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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