FDA Device Establishments · JSON-LD · Markdown
FEI 3004097451 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3004097451 |
|---|---|
| Owner / Operator | STERIS Corporation (#10078069) |
| Address | 490 Boulevard Armand-Paris, QUEBEC, G1C 8A3, CA |
| Mandatory US Agent | STERIS Corporation |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NZA |
| Regulation § (21 CFR) | 876.1500 |
| Proprietary names | Flow Unit 11 (QB-MF); Flow Unit 8 (QB-MF); Flow Unit 5 (QB-MF); Reliance DG Dry Germicide (5100) (MM-CFE); Flow Unit 2 (QB-MF); Flow Unit 1 (QB-MF); Flow Unit 10 (QB-MF); Flow Unit 7 (QB-MF); Flow Unit 6 (QB-MF); Flow Unit 3 (QB-MF) |
Source: openFDA. Public-domain (CC0).