FDA Device Establishments · JSON-LD · Markdown
FEI 3031572059 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3031572059 |
|---|---|
| Owner / Operator | TissueGUARD GmbH (#10090875) |
| Address | Hohe Str 6, Dresden Saxony, 01069, DE |
| Mandatory US Agent | EMG Consulting Services |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HMX |
| Regulation § (21 CFR) | 886.4350 |
| Proprietary names | TissueGUARD DMEK Injector SET |
Source: openFDA. Public-domain (CC0).