Establishment registration
EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
FDA establishment registration 3003268355 · Luebeck Schleswig-Holstein, DE
Key facts
| Registration number | 3003268355 |
|---|---|
| Establishment name | EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG |
| Owner/operator | EUROIMMUN Medizinische Labordiagnostika AG |
| Owner/operator number | 10025212 |
| FEI number | 3003268355 |
| Address | EUROIMMUN AG |
| City | Luebeck Schleswig-Holstein |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | DBM, DHN, GNH, GNM, GNS, GOA, GOX, GPE, GQT, GSM, IBK, JJE, JQT, JQW, KEI, KTL, LEB, LJB, LJM, LJY, LJZ, LKO, LKP, LLL, LRM, LSR, LXG, MCE, MDJ, MDT and 21 more |
| Device classes | 1, 2, N |
At a glance
- 10–99 Device listings
- 1,000+ 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