FDA Device Establishments · JSON-LD · Markdown
FEI 3002931663 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3002931663 |
|---|---|
| Owner / Operator | DILON TECHNOLOGIES Inc (#9035906) |
| Address | 701 Mariners Row, Suite 200, NEWPORT NEWS, VA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | PMX |
| Regulation § (21 CFR) | 878.4490 |
| Proprietary names | HEMOBLAST Bellows |
Source: openFDA. Public-domain (CC0).