FDA Device Establishments · JSON-LD · Markdown
FEI 3007962724 · Manufacture Medical Device Remanufacture Medical Device · Status: Active
| FEI Number | 3007962724 |
|---|---|
| Owner / Operator | NIHON KOHDEN CORP. (#8030227) |
| Address | 486 Nanokaichi, Gunma Tokyo, 370-2343, JP |
| Mandatory US Agent | NIHON KOHDEN AMERICA, LLC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KOI |
| Regulation § (21 CFR) | 868.2775 |
| Proprietary names | Data Acquisition Unit; Life Scope® CSM-1901 Bedside Monitoring Systems; AY Input Unit Series; Life Scope® PT BSM-1700 Series; Life Scope® BSM 6000 Series Bedside Monitoring Systems |
Source: openFDA. Public-domain (CC0).