FDA Device Establishments · JSON-LD · Markdown

ORTEK AG

FEI 3003061090 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3003061090
Owner / OperatorORTEK AG (#9064081)
AddressINDUSTRIE NORD 5, MERENSCHWAND Aargau, CH-5634, CH
Mandatory US AgentFDAbasics
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)LPH
Regulation § (21 CFR)888.3358

External sources

Source: openFDA. Public-domain (CC0).