FDA Device Establishments · JSON-LD · Markdown
FEI 3004858034 · Manufacture Medical Device · Status: Active
| FEI Number | 3004858034 |
|---|---|
| Owner / Operator | ZIEMER OPHTHALMIC SYSTEMS AG (#9067737) |
| Address | ALLMENDSTRASSE 11, PORT Bern, CH - 2562, CH |
| Mandatory US Agent | Regulatory Insight, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | GEX, HNO |
| Regulation § (21 CFR) | 878.4810, 886.4370 |
| Proprietary names | Procedure Packs LCS; Intershield for LCS; FEMTO Crystal Line; Procedure Packs |
Source: openFDA. Public-domain (CC0).