# CLERAD

FEI: 3009518669
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
Owner/operator: CLERAD (#10041828)

Address: 184-186 avenue Gustave Flaubert, Clermont-Ferrand Puy-de-Dome, 63000, FR

Mandatory US Agent: MINVASIVE SURGICAL

## Products

Total registered: 1
Top product codes: IZD
Regulation §: 892.1320

Proprietary names: KUBTEC GammaPRO, GAMMA SUP II

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009518669%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009518669