FDA Device Establishments · JSON-LD · Markdown
FEI 3012481881 · Manufacture Medical Device · Status: Active
| FEI Number | 3012481881 |
|---|---|
| Owner / Operator | AKTIVE SRL (#10087294) |
| Address | VIA GIACOMO DELITALA, 106, Rome Lazio, 00173, IT |
| Mandatory US Agent | Registrar corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HND |
| Regulation § (21 CFR) | 886.4350 |
| Proprietary names | Delamination Spatula 25G; Retinal Pic 25G; Retinal Pic 20G; Retinal Scraper 25G Full Handle; Retinal Scraper 23G Full Handle; Retinal Pic 23G; Retinal Scraper 20G Full Handle; Retinal Pic 27G; Retinal Scraper 27G Full Handle; Delamination Spatula 23G |
Source: openFDA. Public-domain (CC0).