# KUEHNE GMBH

FEI: 3009963139
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Repack or Relabel Medical Device
Owner/operator: Kuehne GmbH (#10088909)

Address: Beratgerstr. 19, Dortmund North Rhine-Westphalia, 44149, DE

Mandatory US Agent: Block Imaging

## Products

Total registered: 3
Top product codes: IZI, OWB, JAA
Regulation §: 892.1600, 892.1650

Proprietary names: Allura Xper FD20/20

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009963139%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009963139