# Arthrex Distribution Hub EMEA B.V.

FEI: 3016851379
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: ARTHREX, INC. (#1220287)

Address: Amperestraat 9, Venlo Limburg, 5928 PE, NL

Mandatory US Agent: Arthrex Inc

## Products

Total registered: 1
Top product codes: MBI
Regulation §: 888.3040


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223016851379%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3016851379