# TEKNIMED SAS

FEI: 3003854593
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Teknimed (#9040657)

Address: 11_12 rue d Apollo, L Union Haute-Garonne, 31240, FR

Mandatory US Agent: Regulatory/Quality Management Information Source, Inc.

## Products

Total registered: 1
Top product codes: NDN
Regulation §: 888.3027


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003854593%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003854593