Establishment registration
ACARIX AS
FDA establishment registration 3019252624 · Hellerup Hovedstaden, DK
Key facts
| Registration number | 3019252624 |
|---|---|
| Establishment name | ACARIX AS |
| Owner/operator | Acarix AS |
| Owner/operator number | 10081966 |
| FEI number | 3019252624 |
| Address | Ryvangs Alle 81-83 |
| City | Hellerup Hovedstaden |
| Country | DK |
| Establishment types | Manufacturer, Specification developer |
| Registration valid through | 2026 |
| Product codes listed | QMW |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 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