FDA Device Establishments · JSON-LD · Markdown
FEI 3003995932 · Manufacture Medical Device · Status: Active
| FEI Number | 3003995932 |
|---|---|
| Owner / Operator | VITROLIFE AB (#9037178) |
| Address | Gustaf Werners Gata 2, Vastra Frolunda Vastra Gotaland, SE-421 32, SE |
| Mandatory US Agent | Vitrolife Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HIO |
| Regulation § (21 CFR) | 884.1550 |
| Proprietary names | Amniocentesis Needle |
Source: openFDA. Public-domain (CC0).