FDA Device Establishments · JSON-LD · Markdown
FEI 3002806833 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3002806833 |
|---|---|
| Owner / Operator | DORNIER MEDTECH GMBH (#8010622) |
| Address | ARGELSRIEDER FELD 7, WESSLING Bavaria, D-82234, DE |
| Mandatory US Agent | DORNIER MEDTECH AMERICA, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LNS |
| Regulation § (21 CFR) | 876.5990 |
| Proprietary names | Gemini 220 XP |
Source: openFDA. Public-domain (CC0).