FDA Device Establishments · JSON-LD · Markdown

K Line Portugal Unipessoal Ltd

FEI 3033492726 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Manufacture Medical Device · Status: Active

FEI Number3033492726
Owner / OperatorK LINE EUROPE GMBH (#10079939)
AddressEstrada de Braga, Lugar de S.Fausto, Armazem 4, Chaves Braga, 5400-283, PT
Mandatory US AgentAclivi, LLC
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)NXC
Regulation § (21 CFR)872.5470

External sources

Source: openFDA. Public-domain (CC0).