FDA Device Establishments · JSON-LD · Markdown

Ambu A/S

FEI 3002806359 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3002806359
Owner / OperatorAMBU A/S (#8010067)
AddressBaltorpbakken 13, Ballerup Hovedstaden, DK-2750, DK
Mandatory US AgentAmbu Inc
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)FDT, FET
Regulation § (21 CFR)876.1500
Proprietary namesAmbu aScope Duodeno 2; Ambu aBox 2

External sources

Source: openFDA. Public-domain (CC0).