FDA Device Establishments · JSON-LD · Markdown
FEI 3000255542 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3000255542 |
|---|---|
| Owner / Operator | STERIS Corporation (#10078069) |
| Address | Unit 7 & 8, Stortford Hall Industrial Park, Dunmow Road, Bishops Stortford Hertfordshire, CM23 5GZ, GB |
| Mandatory US Agent | STERIS Corporation |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MEC |
| Regulation § (21 CFR) | 880.6992 |
| Proprietary names | VERIFY All Clean Test Washer Indicator Holder (LCC010) (LC-MF); VERIFY All Clean Test Washer Indicator (LCC012) (LC-MF); Universal Rack - Cart Washer (FD372) (QB-MF); 4-Level Single-Chamber Manifold Rack (FD75000) (QB-MF); ROBOTIC BASKET FOR PCF XI DROP+LOCK (MD-MF); 1 Level General Purpose Rack (CM53) (QB-MF); Multi-function Rack for Small Items (FD115) (QB-MF); Tray Rack without Hooks (CM55) (QB-MF); PCF PRO and Basket (MED11180USA) (MD-CFE); AMSCO 2532 4 Level Manifold Rack (FD039) (QB-MF) |
Source: openFDA. Public-domain (CC0).