1,546 results
·
34ms
·
Sources: EU EUDAMED, US FDA
MC 3FP-S Spritzekopf (gerade) / US-Version
Device
EU MDR
·
Eu Md Class 2a
·Mytronic GmbH·Not intended for eu market
MC 3FP-S Spritzekopf (gerade) / US-Version
Device
EU MDR
·
Eu Md Class 2a
·Mytronic GmbH·Not intended for eu market
MC 3FP-S Spritzekopf (gerade) / US-Version
Device
EU MDR
·
Eu Md Class 2a
·Mytronic GmbH·Not intended for eu market
MC 3FP-S Spritzekopf (gerade) / US-Version
Device
EU MDR
·
Eu Md Class 2a
·Mytronic GmbH·Not intended for eu market
MC 3FP-S Spritzekopf (gerade) / US-Version
Device
EU MDR
·
Eu Md Class 2a
·Mytronic GmbH·Not intended for eu market
MC 3FP-S Spritzekopf (gerade) / US-Version
Device
EU MDR
·
Eu Md Class 2a
·Mytronic GmbH·Not intended for eu market
MC 3FP Spritze (gera-de) ohne Schlauch
Device
EU MDR
·
Eu Md Class 2a
·On the market
MC 3FP-S Spritzekopf (gerade) / US-Version
Device
EU MDR
·
Eu Md Class 2a
·Not intended for eu market
MC 3FP-S Spritzekopf (gerade) / US-Version
Device
EU MDR
·
Eu Md Class 2a
·Not intended for eu market
Access AFP (300 & 600 Test Kit)
Device
EU IVDR
·
Eu Ivd Class C
·Beckman Coulter Inc.·On the market·32 countries
Access AFP (300 & 600 Test Kit)
Device
EU IVDR
·
Eu Ivd Class C
·Beckman Coulter Inc.·On the market·32 countries
Enzyme Immunoassay, Fetal Fibronectin
FDA Pre-Market Approval
FDA Class 3
·Rapid fFN Cassette Kit for the TLiIQ System, Rapid fFN Control for the TLiIQ System
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·ARCHITECT HBSAG QUALITATIVE(LN 4P53), ARCHITECT HBSAG QUALITATIVE CONFIRMATORY (LN 4P54) ASSAYS
SteriScan Steam Integrator (1100) (FP-CM, HP-CM)
FDA registration
STERIS Corporation·1 product·🇺🇸 United States
SteriScan Steam Integrator (1100) (FP-CM, HP-CM)
FDA registration
STERIS Corporation·1 product·🇺🇸 United States
Kit, Test, Alpha-Fetoprotein For Neural Tube Defects
FDA Pre-Market Approval
FDA Class 3
·GAMMA DAB (125I) AFP RIA KIT
Enzyme Immunoassay, Fetal Fibronectin
FDA Pre-Market Approval
FDA Class 3
·Rapid fFN for the TLiIQ System
Enzyme Immunoassay, Fetal Fibronectin
FDA Pre-Market Approval
FDA Class 3
·Rapid fFN for the TLiIQ System
Enzyme Immunoassay, Fetal Fibronectin
FDA Pre-Market Approval
FDA Class 3
·Rapid fFN for the TLiIQ System
Kit, Test, Alpha-Fetoprotein For Neural Tube Defects
FDA Pre-Market Approval
FDA Class 3
·GAMMA DAB (125I) AFP RIA KIT