FDA Device Establishments · JSON-LD · Markdown

NIPRO CORPORATION

FEI 3000247873 · Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3000247873
Owner / OperatorNIPRO CORPORATION (#8030375)
Address3-26, Senriokashinmachi, Settsu Osaka, 566-8510, JP
Mandatory US AgentNIPRO MEDICAL CORPORATION
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FJK
Regulation § (21 CFR)876.5820
Proprietary namesNipro blood tubing set; Nipro Set - Blood Tubing Set with Transducer Protector and Priming Set

External sources

Source: openFDA. Public-domain (CC0).