# K Line Portugal Unipessoal Ltd

FEI: 3033492726
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: K LINE EUROPE GMBH (#10079939)

Address: Estrada de Braga, Lugar de S.Fausto, Armazem 4, Chaves Braga, 5400-283, PT

Mandatory US Agent: Aclivi, LLC

## Products

Total registered: 1
Top product codes: NXC
Regulation §: 872.5470


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223033492726%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3033492726