FDA Device Establishments · JSON-LD · Markdown

ITEK

FEI 3014263632 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3014263632
Owner / OperatorITEK (#10087095)
AddressZona Franca La Lima, Edificio MT4, Cartago, 30106, CR
Mandatory US AgentDD Global MedDev Consulting
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)MHX, FLL
Regulation § (21 CFR)870.1025, 880.2910
Proprietary namesCelsi Monitor

External sources

Source: openFDA. Public-domain (CC0).