FDA Device Establishments · JSON-LD · Markdown
FEI 3008918179 · Manufacture Medical Device · Status: Active
| FEI Number | 3008918179 |
|---|---|
| Owner / Operator | NEMOTO KYORINDO CO., LTD. (#9043772) |
| Address | 2-12-23 Aoki, Kawaguchi Plant, KAWAGUCHI-SHI Saitama, 332-0031, JP |
| Mandatory US Agent | NEMOTO MEDICAL U.S., INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DXT |
| Regulation § (21 CFR) | 870.1650 |
| Proprietary names | PRESS DUO elite AG; PRESS DUO elite |
Source: openFDA. Public-domain (CC0).