Establishment registration
DAYE (ANNE'S DAY LTD)
FDA establishment registration 3036679730 · London London, City of, GB
Key facts
| Registration number | 3036679730 |
|---|---|
| Establishment name | DAYE (ANNE'S DAY LTD) |
| Owner/operator | Daye (Anne's Day Ltd) |
| Owner/operator number | 10088636 |
| FEI number | 3036679730 |
| Address | 4th Floor |
| City | London London, City of |
| Country | GB |
| Registration valid through | 2026 |
| Product codes listed | HEB, HHD, KXF |
| 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