FDA Device Establishments · JSON-LD · Markdown
FEI 3009082125 · Manufacture Medical Device · Status: Active
| FEI Number | 3009082125 |
|---|---|
| Owner / Operator | DAINIPPON SEIKI CO., Ltd. (#10090054) |
| Address | Tanatsugu 8 Kotari, Nagaokakyo Kyoto, 6170833, JP |
| Mandatory US Agent | IUVO Consulting, LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KFL |
| Regulation § (21 CFR) | 864.3010 |
| Proprietary names | FFPE Sample Block Automatic Facing Device; Auto Slide Preparation System |
Source: openFDA. Public-domain (CC0).