FDA Device Establishments · JSON-LD · Markdown
FEI 3005128583 · Remanufacture Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3005128583 |
|---|---|
| Owner / Operator | MIE GMBH (#9028781) |
| Address | HAUPTSTR. 112, SETH Schleswig-Holstein, 23845, DE |
| Mandatory US Agent | MiE America Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KPS |
| Regulation § (21 CFR) | 892.1200 |
| Proprietary names | ECAM SCINTRON |
Source: openFDA. Public-domain (CC0).