FDA Device Establishments · JSON-LD · Markdown
FEI 3002299608 · Reprocess Single-Use Device · Status: Active
| FEI Number | 3002299608 |
|---|---|
| Owner / Operator | Medline ReNewal (#9033518) |
| Address | 1500 NE Hemlock Avenue, Redmond, OR, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FZT |
| Regulation § (21 CFR) | 878.4800 |
Source: openFDA. Public-domain (CC0).