FDA Device Establishments · JSON-LD · Markdown
FEI 3010539382 · Repack or Relabel Medical Device Reprocess Single-Use Device · Status: Active
| FEI Number | 3010539382 |
|---|---|
| Owner / Operator | Global Source RX (#10045411) |
| Address | 14505 North Hayden Road, suite 101, Scottsdale, AZ, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | NJH |
| Regulation § (21 CFR) | 886.5844 |
| Proprietary names | Epik Day; Epik Variable; Epik Standard; Epik Office; Epik Single Vision; Epik Lenses |
Source: openFDA. Public-domain (CC0).