FDA Device Establishments · JSON-LD · Markdown

Kitazato Corporation

FEI 3008456389 · Export Device to the United States But Perform No Other Operation on Device Manufacture Medical Device · Status: Active

FEI Number3008456389
Owner / OperatorKitazato Corporation (#10045322)
Address1-1-8 Shibadaimon, Minato-ku Tokyo, 105-0012, JP
Mandatory US AgentEmergo Global Representation LLC
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)MQF
Regulation § (21 CFR)884.6110
Proprietary namesKitazato IUI Catheter with Outer Stiffener with or without Stylet Cannula, 10 cm, model number Type 4-v3 and Type 4-v4; Kitazato IUI Catheter with Outer Stiffener with Stainless Steel Core, 18 cm, model number Type 5-v1 and Type 5-v2; Kitazato IUI Catheter with Outer Stiffener with Stainless Steel Core, 10 cm, model number Type 5-v3 and Type 5-v4; Kitazato IUI Catheter with Outer Stiffener with or without Stylet Cannula, 18 cm, model number Type 4-v1 and Type 4-v2

External sources

Source: openFDA. Public-domain (CC0).