Establishment registration
MERCK KGAA
FDA establishment registration 9610140 · DARMSTADT Hesse, DE
Key facts
| Registration number | 9610140 |
|---|---|
| Establishment name | MERCK KGAA |
| Owner/operator | Merck Life Science KGaA |
| Owner/operator number | 8010686 |
| FEI number | 3002806906 |
| Address | 250 FRANKFURTER STRASSE |
| City | DARMSTADT Hesse |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | GGH, GMZ, HYB, HYC, HYF, HYI, HYJ, HYK, HYL, HYO, HYS, HYZ, HZA, HZF, HZG, HZH, HZJ, HZO, HZR, HZS, HZT, HZX, HZY, IAB, IAC, IAD, IAF, IAM, ICC, ICF and 40 more |
| Device classes | 1 |
At a glance
- 10–99 Device listings
- None UDI devices (GUDID)
- Current Registration current
- 10–99 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