Establishment registration
VITREQ BV
FDA establishment registration 3012037425 · Vierpolders Zuid-Holland, NL
Key facts
| Registration number | 3012037425 |
|---|---|
| Establishment name | VITREQ BV |
| Owner/operator | VITREQ BV |
| Owner/operator number | 10050448 |
| FEI number | 3012037425 |
| Address | Seggelant-Noord 2 |
| City | Vierpolders Zuid-Holland |
| Country | NL |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | FFY, GAA, HMX, HND, HNF, HNR, HNX, HPS, HQB, HQF, MPA |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 100–999 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