FDA Device Establishments · JSON-LD · Markdown
FEI 3009107689 · Manufacture Medical Device · Status: Active
| FEI Number | 3009107689 |
|---|---|
| Owner / Operator | Vitrolife A/S (#10040532) |
| Address | Jens Juuls Vej 16, Viby J Midtjylland, 8260, DK |
| Mandatory US Agent | Vitrolife Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 3 |
| Product codes (top 20) | MQG, MQK, MTX |
| Regulation § (21 CFR) | 884.6120, 884.6160, 884.6190 |
| Proprietary names | EmbryoScope Version D and EmbryoSlide |
Source: openFDA. Public-domain (CC0).