FDA Device Establishments · JSON-LD · Markdown
FEI 3004982543 · Manufacture Medical Device · Status: Active
| FEI Number | 3004982543 |
|---|---|
| Owner / Operator | Wilson Wolf Manufacturing Corporation (#10033706) |
| Address | 2100 Old Highway 8 NW, New Brighton, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KJF |
| Regulation § (21 CFR) | 864.2240 |
| Proprietary names | G-Rex50M Open System, Sterile Fluid Path (P/N 80550); G-Rex50M-CS Closed System, Sterile Fluid Path (P/N 80550-CS); G-Rex50M-TF, Research Use Only Product (P/N RU80550-TF); G-Rex50M-TF, Sterile Fluid Path (P/N 80550-TF); G-Rex500M-CS (P/N 85500S-CS); G-Rex100M-CS (P/N 81100-CS); G-Rex100M (P/N 81100S, 81100); G-Rex100 (P/N 80500S, 80500); G-Rex10 Open System, Sterile Fluid Path (P/N 80040S); G-Rex6 Well Plate (P/N 80240M) |
Source: openFDA. Public-domain (CC0).