Establishment registration
USTOMED INSTRUMENTE GMBH & CO. KG
FDA establishment registration 3002808270 · Tuttlingen Baden-Wurttemberg, DE
Key facts
| Registration number | 3002808270 |
|---|---|
| Establishment name | USTOMED INSTRUMENTE GMBH & CO. KG |
| Owner/operator | USTOMED INSTRUMENTE GMBH & CO. KG |
| Owner/operator number | 10048936 |
| FEI number | 3002808270 |
| Address | Bischof Sproll Str. 2 |
| City | Tuttlingen Baden-Wurttemberg |
| Country | DE |
| Establishment types | Contract manufacturer, Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | BZB, CCW, DZM, DZN, DZP, EAX, EBH, ECB, ECS, EEF, EFK, EFL, EGN, EHY, EHZ, EIB, EID, EIF, EIK, EIS, EIX, EIY, EJB, EJE, EJG, EJL, EJY, EKC, EKF, EKH and 60 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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