Establishment registration
Agilent Technologies Denmark ApS
FDA establishment registration 9610099 · GLOSTRUP Hovedstaden, DK
Key facts
| Registration number | 9610099 |
|---|---|
| Establishment name | Agilent Technologies Denmark ApS |
| Owner/operator | Agilent Technologies, Inc |
| Owner/operator number | 10038794 |
| FEI number | 3002806778 |
| Address | 42 PRODUKTIONSVEJ |
| City | GLOSTRUP Hovedstaden |
| Country | DK |
| Establishment types | Foreign exporter, Foreign private label distributor |
| Registration valid through | 2026 |
| Product codes listed | CZN, CZP, CZS, CZW, DAO, DBI, DDZ, DEH, DEO, DES, DEW, DFH, DFS, DGK, DGR, GGK, GKZ, HYB, HYJ, JIT, JJX, JMR, JZG, JZJ, KEM, KES, KEW, KPA, LEB, LEE and 11 more |
| Device classes | 1, 2, 3, N |
At a glance
- 10–99 Device listings
- 100–999 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