FDA Device Establishments · JSON-LD · Markdown
FEI 3012883081 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3012883081 |
|---|---|
| Owner / Operator | Crosmed S.A. (#10085790) |
| Address | Aguirre 545, Buenos Aires, 1414, AR |
| Mandatory US Agent | Arthrex Inc |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GAT |
| Regulation § (21 CFR) | 878.5000 |
Source: openFDA. Public-domain (CC0).