# CROSMED S.A.

FEI: 3012883081
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: Crosmed S.A. (#10085790)

Address: Aguirre 545, Buenos Aires, 1414, AR

Mandatory US Agent: Arthrex Inc

## Products

Total registered: 1
Top product codes: GAT
Regulation §: 878.5000


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012883081%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012883081