Establishment registration
VITROLIFE SWEDEN AB
FDA establishment registration 3003995932 · Vastra Frolunda Vastra Gotaland, SE
Key facts
| Registration number | 3003995932 |
|---|---|
| Establishment name | VITROLIFE SWEDEN AB |
| Owner/operator | VITROLIFE AB |
| Owner/operator number | 9037178 |
| FEI number | 3003995932 |
| Address | Gustaf Werners Gata 2 |
| City | Vastra Frolunda Vastra Gotaland |
| Country | SE |
| Registration valid through | 2026 |
| Product codes listed | GAZ, HIO, ITX, MQE, MQF, MQK, MQL, PUC, PUD, QKI |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ 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