Establishment registration
GRUPPO BIOIMPIANTI S.R.L.
FDA establishment registration 3007391088 · Peschiera Borromeo Milano, IT
Key facts
| Registration number | 3007391088 |
|---|---|
| Establishment name | GRUPPO BIOIMPIANTI S.R.L. |
| Owner/operator | Gruppo Bioimpianti S.r.l. |
| Owner/operator number | 10051817 |
| FEI number | 3007391088 |
| Address | Via Liguria 28 |
| City | Peschiera Borromeo Milano |
| Country | IT |
| Registration valid through | 2026 |
| Product codes listed | LZO, MEH |
| Device classes | 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