FDA Device Establishments · JSON-LD · Markdown
FEI 3015328411 · Remanufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device Repack or Relabel Medical Device · Status: Active
| FEI Number | 3015328411 |
|---|---|
| Owner / Operator | Murata Vios, Inc. (#10059850) |
| Address | 700 Commerce Drive, Suite 190, Woodbury, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 4 |
| Product codes (top 20) | DRT, DRG, DPZ, DQA |
| Regulation § (21 CFR) | 870.2300, 870.2910, 870.2710, 870.2700 |
| Proprietary names | Vios Monitoring System Model 2050 |
Source: openFDA. Public-domain (CC0).