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COLOPLAST MANUFACTURING FRANCE, SAS

FEI 3002807917 · Manufacture Medical Device · Status: Active

FEI Number3002807917
Owner / OperatorColoplast Corp. (#8010144)
Address9 Avenue Edmond Rostand, CS 70218, Sarlat la Caneda Cedex Dordogne, 24206, FR
Mandatory US AgentCOLOPLAST CORP
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FAD
Regulation § (21 CFR)876.4620
Proprietary namesVortek Hydrocoated Double Loop Ureteral Stent

External sources

Source: openFDA. Public-domain (CC0).