FDA Device Establishments · JSON-LD · Markdown
FEI 3006493760 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3006493760 |
|---|---|
| Owner / Operator | icotec ag (#10042564) |
| Address | Industriestrasse 12, Altstaetten Sankt Gallen, 9450, CH |
| Mandatory US Agent | MCRA, LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | PML, KWQ |
| Regulation § (21 CFR) | 888.3027, 888.3060 |
Source: openFDA. Public-domain (CC0).