FDA Device Establishments · JSON-LD · Markdown
FEI 3002835648 · Manufacture Medical Device · Status: Active
| FEI Number | 3002835648 |
|---|---|
| Owner / Operator | V. GULDMANN A/S (#9027662) |
| Address | GRAHAM BELLS VEJ 23 A, AARHUS N Midtjylland, DK-8200, DK |
| Mandatory US Agent | Guldmann Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FSA |
| Regulation § (21 CFR) | 880.5510 |
| Proprietary names | GH3 Twin Patient Lift; GH1 F Patient Lift; GH1 Patient Lift; GL5.2 Patient Floor Lift; GH3 Patient Lift; GH1 Q Patient Lift; GHZ Patient Lift; GLS5.2 Sit to Stand Floor Lifter; GH3+ Patient Lift |
Source: openFDA. Public-domain (CC0).