Establishment registration
MEDITEC SOURCE GmbH & Co. KG
FDA establishment registration 3009468807 · Tuttlingen-Nendingen Baden-Wurttemberg, DE
Key facts
| Registration number | 3009468807 |
|---|---|
| Establishment name | MEDITEC SOURCE GmbH & Co. KG |
| Owner/operator | Meditec Source GmbH & Co. KG |
| Owner/operator number | 10041453 |
| FEI number | 3009468807 |
| Address | Sattlerstrasse 19 |
| City | Tuttlingen-Nendingen Baden-Wurttemberg |
| Country | DE |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | FCZ, FHQ, FSM, FTY, FZT, FZX, GAD, GDZ, GEG, GEN, GFA, HRR, HTC, HTD, HTE, HTF, HTJ, HTR, HTW, HTX, HTZ, HWT, HWX, HXW, HXX, HXZ, LXH, MDM, MNH, MNI |
| Device classes | 1, 2 |
At a glance
- 10–99 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