FDA Device Establishments · JSON-LD · Markdown
FEI 1218444 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 1218444 |
|---|---|
| Owner / Operator | ABBOTT LABORATORIES (#1415939) |
| Address | 23 4th Ave, BURLINGTON, MA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 7 |
| Product codes (top 20) | DTZ, KRI, KFM, DWA, DTQ, DTR, DWF |
| Regulation § (21 CFR) | 870.4350, 870.4200, 870.4360, 870.4380, 870.4220, 870.4240, 870.4210 |
| Proprietary names | CentriMag Pre-connected Pack |
Source: openFDA. Public-domain (CC0).