Establishment registration
DIMEDA INSTRUMENTE GMBH
FDA establishment registration 9611283 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9611283 |
|---|---|
| Establishment name | DIMEDA INSTRUMENTE GMBH |
| Owner/operator | DIMEDA INSTRUMENTE GMBH |
| Owner/operator number | 8010631 |
| FEI number | 3002806816 |
| Address | GANSACKER 54 + 58 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BSY, BWB, CBH, CCQ, CCW, DWH, DWS, DZC, EAX, ECS, ECT, EEF, EFK, EFL, EGN, EIC, EIG, EIK, EIR, EIS, EIX, EIY, EJG, EJY, EJZ, EKB, EKD, EKE, EKG, EKH and 223 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 10–99 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