FDA Device Establishments · JSON-LD · Markdown
FEI 3015905920 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3015905920 |
|---|---|
| Owner / Operator | Powder Design, LTD (#10084120) |
| Address | 17/1 Silvermills Court, Henderson Place Lane, Edinburgh Midlothian, EH3 5DG, GB |
| Mandatory US Agent | Registrar Corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQY |
| Regulation § (21 CFR) | 886.5850 |
| Proprietary names | Powder |
Source: openFDA. Public-domain (CC0).