FDA Device Establishments · JSON-LD · Markdown
FEI 3012885391 · Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3012885391 |
|---|---|
| Owner / Operator | Nucleix Ltd. (#10088381) |
| Address | 3 Pekeris Street, Rehovot Central, 7670203, IL |
| Mandatory US Agent | Nucleix Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MMW |
| Regulation § (21 CFR) | 866.6010 |
| Proprietary names | Bladder EpiCheck |
Source: openFDA. Public-domain (CC0).