FDA Device Establishments · JSON-LD · Markdown
FEI 3013501110 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3013501110 |
|---|---|
| Owner / Operator | NIHON KOHDEN CORP. (#8030227) |
| Address | 1-1-6 Kusunokidai, Tokorozawa-Shi, Saitama, Tokorozawa Saitama, 359-0037, JP |
| Mandatory US Agent | NIHON KOHDEN AMERICA, LLC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 8 |
| Product codes (top 20) | CBS, NHQ, NHP, CBR, CBQ, CCL, CCK, NHO |
| Regulation § (21 CFR) | 868.1620, 868.1500, 868.1700, 868.1720, 868.1400 |
| Proprietary names | AG-920RA Mulitgas Unit; AG-920RA |
Source: openFDA. Public-domain (CC0).