FDA Device Establishments · JSON-LD · Markdown

LIKO AB

FEI 3000230206 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3000230206
Owner / OperatorBAXTER HEALTHCARE CORPORATION (#1417572)
AddressNedre vagen 100, LULEA Norrbotten, 975 92, SE
Mandatory US AgentBAXTER HEALTHCARE CORPORATION
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)IKX
Regulation § (21 CFR)890.5050
Proprietary namesHANDYBELT; HANDYTUBE; HANDYSHEET

External sources

Source: openFDA. Public-domain (CC0).