FDA Device Establishments · JSON-LD · Markdown
FEI 3002991496 · Foreign Private Label Distributor Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3002991496 |
|---|---|
| Owner / Operator | Carl Zeiss Meditec AG (Jena) (#9053564) |
| Address | 20-22 RUE LOUIS ARMAND, PARIS Ile-de-France, 75015, FR |
| Mandatory US Agent | CARL ZEISS MEDITEC USA, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FFS |
| Regulation § (21 CFR) | 876.1500 |
| Proprietary names | Wide Angle Fiber Optic Probe, Ocutome 5 mm connector; Chandelier with Adjustable ring, Bausch & Lomb Stellaris PC; Chandelier with Adjustable ring, Ocutome 5 mm connector; Wide Angle Fiber Optic Probe, Alcon Accurus; Chandelier with Adjustable ring, Alcon Constellation; Focus Fiber Optic Probe, Alcon Accurus; Fiber Optic Probe, Ocutome 5 mm connector; Wide Angle Fiber Optic Probe, Bausch & Lomb; Shielded Fiber Optic Probe, Ocutome 5 mm connector; Wide Angle Fiber Optic Probe, Bausch & Lomb Stellaris PC |
Source: openFDA. Public-domain (CC0).