FDA Device Establishments · JSON-LD · Markdown
FEI 3038188186 · Manufacture Medical Device · Status: Active
| FEI Number | 3038188186 |
|---|---|
| Owner / Operator | PURTEX s.r.o. (#10092884) |
| Address | Ustecka 103, Zdiby Praha-Vychod, 25066, CZ |
| Mandatory US Agent | MAK and Associates, LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FNM |
| Regulation § (21 CFR) | 880.5550 |
| Proprietary names | HybriMatt 200 |
Source: openFDA. Public-domain (CC0).