# NIPRO CORPORATION

FEI: 3000247873
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: NIPRO CORPORATION (#8030375)

Address: 3-26, Senriokashinmachi, Settsu Osaka, 566-8510, JP

Mandatory US Agent: NIPRO MEDICAL CORPORATION

## Products

Total registered: 1
Top product codes: FJK
Regulation §: 876.5820

Proprietary names: Nipro blood tubing set, Nipro Set - Blood Tubing Set with Transducer Protector and Priming Set

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223000247873%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3000247873