Establishment registration
ZEPF MEDICAL INSTRUMENTS GMBH
FDA establishment registration 3003244954 · SEITINGEN-OBERFLACHT Baden-Wurttemberg, DE
Key facts
| Registration number | 3003244954 |
|---|---|
| Establishment name | ZEPF MEDICAL INSTRUMENTS GMBH |
| Owner/operator | ZEPF MEDICAL INSTRUM |
| Owner/operator number | 9045716 |
| FEI number | 3003244954 |
| Address | 21 GUNNINGER ST. |
| City | SEITINGEN-OBERFLACHT Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | CCQ, DWS, EAX, ECS, EFK, EFL, EGN, EIG, EIS, EIY, EJG, EKG, EKI, EMF, EMG, EMH, EMI, EMJ, EML, EMR, EPE, EPY, ERA, FAX, FFO, FFQ, FHA, FNS, FNY, FSM and 101 more |
| Device classes | 1 |
At a glance
- 100–999 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