# TECHNOFLEX SAS

FEI: 3039404452
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: TECHNOFLEX SAS (#10093662)

Address: 69 ZA deBassilour, BIDART Nouvelle-Aquitaine, 64210, FR

Mandatory US Agent: mdi Consultants, Inc.

## Products

Total registered: 1
Top product codes: KPE
Regulation §: 880.5025


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223039404452%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3039404452