FDA.reportPublic FDA data

KOFU FACTORY OF TERUMO CORP.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
96818353003752255KOFU FACTORY OF TERUMO CORP.1N2026-01-011727-1 TSUIJIARAI, SHOWA-CHO NAKAKOMA-GUN Yamanashi JP 409-3853

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
88941760146173K991406TERUMO SURFLO FLEX I.V. CATHETER AND TERUMO SURFLASH I.V. CATHETERFOZ1999-06-16
88941623404593K983490TERUMO VENOJECT,LUER ADAPTERJKA1998-11-30
88941809451363K771204SURFLO WINGED INFUSION SETFPA1977-07-14
88941248316198K190427ImmuciseFMF2019-07-18
88941956625362K100282TERUMO SURSHIELD- PUR SAFETY I.V. CATHETERFOZ2010-02-26
88941000357614BK970008

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FOZ22010-02-26
FMF12019-07-18
JKA11998-11-30
FPA11977-07-14

PMN#