# Procept Biorobotics c/o HealthLink Europe B.V.

FEI: 3043534483
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: PROCEPT BioRobotics Corporation (#10055490)

Address: Mechie Trommelenweg 8, Waalwijk Noord-Brabant, 5145 ND, NL

Mandatory US Agent: PROCEPT BIOROBOTICS CORPORATION

## Products

Total registered: 1
Top product codes: EYY
Regulation §: 878.4370

Proprietary names: Lithotomy Drape, Aquablation Essential Drape Pack, DR2500

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223043534483%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3043534483