FDA Device Establishments · JSON-LD · Markdown
FEI 3019575688 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3019575688 |
|---|---|
| Owner / Operator | Aktiia SA (#10092031) |
| Address | Rue du Bassin 8a,, Neuchatel, 2000, CH |
| Mandatory US Agent | Neil Puri |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DXN |
| Regulation § (21 CFR) | 870.1130 |
| Proprietary names | G0 Blood Pressure Monitoring System; Hilo Cuff |
Source: openFDA. Public-domain (CC0).