FDA Device Establishments · JSON-LD · Markdown
FEI 3003936139 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3003936139 |
|---|---|
| Owner / Operator | PFM Medical Titanium (#9055994) |
| Address | Sudwestpark 42, NUREMBERG Bavaria, 90449, DE |
| Mandatory US Agent | PFM Medical, Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | FTL, OXJ |
| Regulation § (21 CFR) | 878.3300 |
| Proprietary names | TiMESH |
Source: openFDA. Public-domain (CC0).