Establishment registration
Sirtex Germany Manufacturing GmbH
FDA establishment registration 3013070673 · Frankfurt am Main Hesse, DE
Key facts
| Registration number | 3013070673 |
|---|---|
| Establishment name | Sirtex Germany Manufacturing GmbH |
| Owner/operator | Sirtex Medical Inc. |
| Owner/operator number | 9047689 |
| FEI number | 3013070673 |
| Address | Industriepark Hoechst, Building G808 |
| City | Frankfurt am Main Hesse |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | IWJ, IWR, IWW, KPY, NAW |
| Device classes | 1, 3 |
At a glance
- 1–9 Device listings
- 10–99 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