Establishment registration
ABBOTT GmbH
FDA establishment registration 3002809144 · Wiesbaden Hesse, DE
Key facts
| Registration number | 3002809144 |
|---|---|
| Establishment name | ABBOTT GmbH |
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| FEI number | 3002809144 |
| Address | Max-Planck-Ring 2 |
| City | Wiesbaden Hesse |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | CDD, CDO, CDP, CDZ, CEC, CEK, CEM, CEO, CEP, CEW, CFJ, CFP, CFR, CFT, CGJ, CGN, CGX, CGZ, CHH, CHI, CHP, CIG, CIT, CIX, CJE, CJW, CKA, CZP, CZW, DAD and 107 more |
| Device classes | 1, 2, 3, N |
At a glance
- 100–999 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