Establishment registration
Terumo BCT Europe N.V.
FDA establishment registration 3010425916 · Leuven Vlaams Brabant, BE
Key facts
| Registration number | 3010425916 |
|---|---|
| Establishment name | Terumo BCT Europe N.V. |
| Owner/operator | Terumo BCT, INC. |
| Owner/operator number | 9002708 |
| FEI number | 3010425916 |
| Address | Medical Electronics |
| City | Leuven Vlaams Brabant |
| Country | BE |
| Establishment types | Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BSB, KSD |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- None 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