FDA Device Establishments · JSON-LD · Markdown
FEI 3005990076 · Manufacture Medical Device · Status: Active
| FEI Number | 3005990076 |
|---|---|
| Owner / Operator | Andreas Hettich GmbH (#9020624) |
| Address | FOEHRENSTRASSE 12, TUTTLINGEN Baden-Wurttemberg, D-78532, DE |
| Mandatory US Agent | HETTICH INSTRUMENTS LP |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | IFB |
| Regulation § (21 CFR) | 864.3300 |
| Proprietary names | Cyto Centrifuge |
Source: openFDA. Public-domain (CC0).