FDA Device Establishments · JSON-LD · Markdown
FEI 3006108784 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3006108784 |
|---|---|
| Owner / Operator | AbbVie, Inc. (#2011068) |
| Address | 900 PARKWAY GLOBAL PARK, LA AURORA DE HEREDIA, 191-3006, CR |
| Mandatory US Agent | ABBVIE, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KDD |
| Regulation § (21 CFR) | 878.4800 |
| Proprietary names | Insertion Sleeve; Keller Funnel; Keller Funnel 2; Fill Tube Kit |
Source: openFDA. Public-domain (CC0).