FDA Device Establishments · JSON-LD · Markdown
FEI 3025308027 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3025308027 |
|---|---|
| Owner / Operator | Biolens Lab (#10086679) |
| Address | Lot N 6 El Farah 2, Mohammedia Mohammadia, 28810, MA |
| Mandatory US Agent | EYEREG CONSULTING INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQD |
| Regulation § (21 CFR) | 886.5916 |
| Proprietary names | BioFlex SA MSP; BioFlex SA TE; BioSclere TE MSP; BioSclere TP MSL; BioK TE; BioK D MSP; BioFlex SA; BioFlex SA TI; BioK D TE; BioK BT |
Source: openFDA. Public-domain (CC0).