Establishment registration
TONTARRA MEDIZINTECHNIK GMBH
FDA establishment registration 9680515 · WURMLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9680515 |
|---|---|
| Establishment name | TONTARRA MEDIZINTECHNIK GMBH |
| Owner/operator | TONTARRA MEDIZINTECHNIK GMBH |
| Owner/operator number | 9009570 |
| FEI number | 3005969827 |
| Address | DAIMLERSTRASSE 15 |
| City | WURMLINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | BWB, DWP, DWS, DXC, DZA, DZN, EFK, EFL, EGN, EIF, EIG, EIR, EIX, EJI, EJY, EKB, EMD, EME, EMF, EMG, EMH, EMI, EMJ, EMM, EMN, EMR, EOQ, EPY, FAJ, FAS and 100 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 100–999 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