Establishment registration
RZ MEDIZINTECHNIK GMBH
FDA establishment registration 9680718 · TUTTLINGEN Baden-Wurttemberg, DE
Key facts
| Registration number | 9680718 |
|---|---|
| Establishment name | RZ MEDIZINTECHNIK GMBH |
| Owner/operator | RZ MEDIZINTECHNIK GMBH |
| Owner/operator number | 9010855 |
| FEI number | 3000280067 |
| Address | UNTER HASSLEN 20/22 |
| City | TUTTLINGEN Baden-Wurttemberg |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DWS, DZN, EBA, EFK, EFL, EGN, EJG, EKR, EMD, EMF, EMG, EMH, EMM, EPY, EQH, EYI, EYK, EZO, FAJ, FAS, FAX, FBM, FBQ, FBX, FCL, FCT, FCW, FFD, FFL, FFN and 161 more |
| Device classes | 1, 2 |
At a glance
- 100–999 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