# COLOPLAST MANUFACTURING FRANCE, SAS

FEI: 3002807917
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Coloplast Corp. (#8010144)

Address: 9 Avenue Edmond Rostand, CS 70218, Sarlat la Caneda Cedex Dordogne, 24206, FR

Mandatory US Agent: COLOPLAST CORP

## Products

Total registered: 1
Top product codes: FAD
Regulation §: 876.4620

Proprietary names: Vortek Hydrocoated Double Loop Ureteral Stent

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002807917%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002807917