Establishment registration
MEDI.PLAN GMBH & CO. KG
FDA establishment registration 3033536319 · Dortmund North Rhine-Westphalia, DE
Key facts
| Registration number | 3033536319 |
|---|---|
| Establishment name | MEDI.PLAN GMBH & CO. KG |
| Owner/operator | MEDI.PLAN GmbH & Co. KG |
| Owner/operator number | 10091549 |
| FEI number | 3033536319 |
| Address | Hofkerstrabe 22 |
| City | Dortmund North Rhine-Westphalia |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | BRZ, BYH, BZG, DPS, DXQ, ERA, ERL, EXH, FLL, FMF, FMG, FMH, FMI, FMP, FOZ, FPA, FPB, FRO, FXY, FYA, GEI, GFA, HBE, HIB, HKM, HLI, HLJ, HLS, HRX, HWE and 16 more |
| Device classes | 1, 2, U |
At a glance
- 10–99 Device listings
- 1,000+ 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