# REEV SAS

FEI: 3029957137
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: REEV (#10089096)

Address: 445 l'Occitane, Labege Haute-Garonne, 31670, FR

Mandatory US Agent: REEV

## Products

Total registered: 1
Top product codes: KQX
Regulation §: 888.1500

Proprietary names: Reev Sense

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223029957137%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3029957137