FDA Device Establishments · JSON-LD · Markdown

ABSORBEST AB

FEI 3008821638 · Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device · Status: Active

FEI Number3008821638
Owner / OperatorAbsorbest AB (#10034338)
AddressKlintvagen 1, Kisa Ostergotland, 59039, SE
Mandatory US AgentEmergo Global Representation LLC
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)NAC
Regulation § (21 CFR)878.4018
Proprietary namesDryMax FOAM; DryMax BORDER; DryMax SOFT; DryMax GENTLE; Absorbest Super Foam

External sources

Source: openFDA. Public-domain (CC0).