FDA Device Establishments · JSON-LD · Markdown
FEI 3005935106 · Manufacture Medical Device · Status: Active
| FEI Number | 3005935106 |
|---|---|
| Owner / Operator | Verax Biomedical Incorporated (#10023050) |
| Address | 2200 West Park Drive Suite 300, Westborough, MA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MZC |
| Regulation § (21 CFR) | 866.2560 |
| Proprietary names | Platelet PGDprime Test |
Source: openFDA. Public-domain (CC0).