FDA Device Establishments · JSON-LD · Markdown
FEI 1000221012 · Manufacture Medical Device · Status: Active
| FEI Number | 1000221012 |
|---|---|
| Owner / Operator | Pentair Filtration Solutions (#9009435) |
| Address | 1350 Hammond Rd, Saint Paul, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | CAH |
| Regulation § (21 CFR) | 868.5260 |
| Proprietary names | DBF23-R Reuseable Main Flow Filter |
Source: openFDA. Public-domain (CC0).