# LINDBERG A/S

FEI: 3003093025
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Owner/operator: LINDBERG A/S (#9043163)

Address: 30 BJARKESVEJ, AABYHOJ Midtjylland, 8230, DK

Mandatory US Agent: The Vision Council

## Products

Total registered: 1
Top product codes: HQY
Regulation §: 886.5850

Proprietary names: LINDBERG SUN, SUN, LINDBERG

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003093025%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003093025