FDA.reportPublic FDA data

Vygon Portugal

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30146637543014663754Vygon Portugal1N2026-01-01Parque Empresarial de Baltar/Parada Rua F 7585-013 Balter-Paredes Porto PT 7585-013

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2203071325727741K981630VYGON DOUBLE LUMEN UMBILICAL CATHETERFOS1998-10-01
2203071430307758K963196VYGON UMBILICAL CATHETHER INSERTION TRAYFOZ1997-09-09
2203071717718718K925854VYGON - ENTERAL FEEDING TUBE - POLYURETHANEKNT1994-05-02
2203071432488089K921374VYGON XRO VENOUS/ARTERIAL UMBILICAL CATHETERFOS1992-10-26
2203071596272302K921352VYGON POLYURETHANE VENOUS/ARTERIAL XRO UMBIL. CATHFOS1992-10-26
2203071274448326K851005XRO UMBILICAL CATHETER-CODE 270FOS1985-05-21
2203071078243648K822879ENTERAL NUTRITION 1KNT1982-11-16
2203071641327647K243361NutrifitFPD2024-12-19
2203071919533320K100163NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXXFPD2011-10-13
2203071278045899K060944NUTRISAFE 2FPD2006-09-15

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FOS41998-10-01
FPD32024-12-19
KNT21994-05-02
FOZ11997-09-09