FDA Device Establishments · JSON-LD · Markdown

ASHITAKA FACTORY OF TERUMO CORP.

FEI 3002808327 · Manufacture Medical Device · Status: Active

FEI Number3002808327
Owner / OperatorTERUMO CORP. (#8010026)
Address150 MAIMAIGI-CHO, FUJINOMIYA Shizuoka, 418-0015, JP
Mandatory US AgentTerumo Medical Corp
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)DQX
Regulation § (21 CFR)870.1330
Proprietary namesRadifocus Glidewire; Glidewire GT; Glidewire Gold

External sources

Source: openFDA. Public-domain (CC0).