FDA Device Establishments · JSON-LD · Markdown

KONICA MINOLTA, INC.

FEI 3004485675 · Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3004485675
Owner / OperatorKONICA MINOLTA, INC. (#9009884)
Address1 SAKURA-MACHI, HINO-SHI Tokyo, 191-8511, JP
Mandatory US AgentKonica Minolta Healthcare Americas, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)MQB
Regulation § (21 CFR)892.1680
Proprietary namesREGIUS Cassette; REGIUS Plate; REGIUS Cassette/Plate; REGIUS MODEL 210

External sources

Source: openFDA. Public-domain (CC0).