FDA Device Establishments · JSON-LD · Markdown
FEI 1016427 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 1016427 |
|---|---|
| Owner / Operator | Cordis US Corp. (#1016427) |
| Address | 14201 N.W. 60TH AVE., Miami Lakes, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | OES |
| Regulation § (21 CFR) | 870.1200 |
| Proprietary names | ANGIOGRAPHIC CATHETERIZATION SET |
Source: openFDA. Public-domain (CC0).