FDA Device Establishments · JSON-LD · Markdown

AB GERMA,SWEDEN

FEI 3007143190 · Manufacture Medical Device · Status: Active

FEI Number3007143190
Owner / OperatorAB GERMA,SWEDEN (#9011616)
AddressBOX 2127, KRISTIANSTAD Skane, 29102, SE
Mandatory US AgentFerno-Washington, Inc
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)NZD
Regulation § (21 CFR)880.6900
Proprietary namesGerma Kangoofix Warming bag; Safety Belt System Kangoofix Peadiatric Ready2go; Germa Kangoofix inner harness

External sources

Source: openFDA. Public-domain (CC0).