FDA Device Establishments · JSON-LD · Markdown

ARCADANT B.V.

FEI 3014054090 · Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3014054090
Owner / Operatorarcadant b.v. (#10056015)
Addressprince albert house, liskeard business park, LIskeard Cornwall, PL14 3US, GB
Mandatory US AgentWILLOW GLEN CONSULTANCY
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)MVN, LPL
Regulation § (21 CFR)886.5925
Proprietary namesCHROMAVIEW EYEFX

External sources

Source: openFDA. Public-domain (CC0).