FDA.reportPublic FDA data

FRESENIUS KABI DEUTSCHLAND GMBH

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
96818193000147578FRESENIUS KABI DEUTSCHLAND GMBH1N2026-01-015 ROBERT-KOCH-STRASSE BAD HERSFELD Hesse DE D-36251

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
165651961927749K221121Volumat Polyethylene I.V. Administration SetFPA2023-06-16
165651809783663K220301Volumat LineFPA2023-06-02
165651377032239K212445freeflex+ Transfer AdapterLHI2022-06-01
165651461767317K162826Encore NeutralFPA2017-06-15
165651053905989K121613AGILIA INFUSION SYSTEMFRN2013-05-01
165651124205599

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FPA32023-06-16
LHI12022-06-01
FRN12013-05-01

PMN#