15 results
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42ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HEMO BIOSCIENCE
FDA registration
HEMO BIOSCIENCE·8 products·🇺🇸 United States
MQC-CAT
FDA UDI
HEMO BIOSCIENCE INC·00858352006139·MQC-CAT is intended for the quality control of ...
Hemo-QC
FDA UDI
HEMO BIOSCIENCE INC·00858352006009·Hemo-QC simulates blood samples and is intended...
MQC
FDA UDI
HEMO BIOSCIENCE INC·00858352006122·MQC is intended for the quality control of rout...
C3 Control Cells
FDA UDI
HEMO BIOSCIENCE INC·00858352006016·C3 Control Cells are used to confirm the reacti...
ELUclear
FDA UDI
HEMO BIOSCIENCE INC·00858352006023·ELUclear elution kit is used to elute antibodie...
BLOOD GROUPING REAGENT SOLIDSCREEN II ANTI-D BLEND
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·February 12, 2016
BLOOD GROUPING REAGENT IH-CARD ANTI-D (DVI+)
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·September 5, 2022
BLOOD GROUPING REAGENT IH-CARD ANTI-D (DVI+)
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·September 5, 2022
REAGENT RED BLOOD CELLS BIOTESTCELL A2
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·March 23, 2022
BLOOD GROUPING REAGENT IH-CARD ABO/D(DVI-)+REV A1,B
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·May 24, 2022
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·March 30, 2018
BLOOD GROUPING REAGENT ERYTYPE® S ABO CONFIRM
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·June 21, 2017
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·November 6, 2018
BLOOD GROUPING REAGENT IH-CARD ABO/D(DVI-)+REV A1,B
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·June 15, 2022