FDA Device Establishments · JSON-LD · Markdown
FEI 3020542149 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3020542149 |
|---|---|
| Owner / Operator | Pulsenmore LTD (#10094113) |
| Address | 8 Omarim St., Omer Southern, 8496500, IL |
| Mandatory US Agent | MedicSense USA LCC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | SGJ |
| Regulation § (21 CFR) | 892.1590 |
| Proprietary names | Pulsenmore ES |
Source: openFDA. Public-domain (CC0).