# ARTA PLAST AB

FEI: 3002807188
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Arta Plast AB (#10051331)

Address: Antennvaegen 1, Tyresoe Stockholm, 13548, SE

Mandatory US Agent: Seerc consulting

## Products

Total registered: 1
Top product codes: KRR
Regulation §: 888.3540

Proprietary names: Femoral Drilling Socket, Patellar Adjustment Socket, Femoral Adjustment Socket

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002807188%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002807188