FDA Device Establishments · JSON-LD · Markdown
FEI 3003950207 · Manufacture Medical Device · Status: Active
| FEI Number | 3003950207 |
|---|---|
| Owner / Operator | STERIS Corporation (#10078069) |
| Address | 6100 Heisley Rd, Mentor, OH, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | MLR |
| Regulation § (21 CFR) | 880.6860 |
| Proprietary names | V-PRO maX 2 Low Temperature Sterilization System (MY-MF, CM-SD); AMSCO V-PRO 1 Low Temperature Sterilization System (MY-CFE); AMSCO V-PRO maX Low Temperature Sterilization System (MY-CFE); VAPROX HC Sterilant (PB007, PB011, PB012) (MM-MF, CM-SD); AMSCO V-PRO 1 PLUS Low Temperature Sterilization System (MY-CFE) |
Source: openFDA. Public-domain (CC0).