Variants of Polyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) by Allmed Middle East
14 variants
DeviceDevice · Manufacturer · Authorizations Verified Status Regime Registry Class
Polyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012797
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012728
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012803
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012735
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012810
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012742
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012827
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012759
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012834
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012766
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012841
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012773
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012858
Regimes: CE MDR Registry: EUDAMEDPolyethersulfone Hollow Fiber Hemodialyzers (BIOPURE LFX and HFX) UDI-DI 06221166012780
Regimes: CE MDR Registry: EUDAMED
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