# Nihon Kohden Tomioka Corporation

FEI: 3007962724
Status: Active
Establishment types: Manufacture Medical Device; Remanufacture Medical Device
Owner/operator: NIHON KOHDEN CORP. (#8030227)

Address: 486 Nanokaichi, Gunma Tokyo, 370-2343, JP

Mandatory US Agent: NIHON KOHDEN AMERICA, LLC.

## Products

Total registered: 1
Top product codes: KOI
Regulation §: 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: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007962724%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007962724