FDA Device Establishments · JSON-LD · Markdown
FEI 3043040746 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3043040746 |
|---|---|
| Owner / Operator | ECLS (#10095020) |
| Address | 190 Carondelet Plz Ste 1450, Saint Louis, MO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EAK |
| Regulation § (21 CFR) | 892.6500 |
| Proprietary names | Protego; ProCart |
Source: openFDA. Public-domain (CC0).