Establishment registration
STILLE AB
FDA establishment registration 3003696170 · Torshalla Sodermanland, SE
Key facts
| Registration number | 3003696170 |
|---|---|
| Establishment name | STILLE AB |
| Owner/operator | STILLE AB |
| Owner/operator number | 9036158 |
| FEI number | 3003696170 |
| Address | Ekbacken 11 |
| City | Torshalla Sodermanland |
| Country | SE |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | DWS, EPY, FHL, FHQ, FZX, FZZ, GAD, GDC, GDH, GDI, GDJ, GDZ, GEA, GEN, HAO, HNF, HRQ, HRR, HRT, HSO, HTE, HTF, HTR, HTS, HTX, HTZ, HXB, HXK, HXL, HXP and 9 more |
| Device classes | 1 |
At a glance
- 10–99 Device listings
- None 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