# KERVIEW S.A.

FEI: 3007120545
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Export Device to the United States But Perform No Other Operation on Device
Owner/operator: KERVIEW S.A. (#10052756)

Address: Ituzaingo 1309 Office 101, MONTEVIDEO, 11000, UY

Mandatory US Agent: The Vision Council

## Products

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


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007120545%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007120545