10,000 results
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79ms
·
Sources: EU EUDAMED, US FDA
Fluorescence In Situ Hybridization, Anaplastic Lymphoma Kinase, Gene Rearrangement
FDA Pre-Market Approval
FDA Class 3
·VYSIS ALK BREAK APART FISH PROBE KIT
System, Test, Her-2/Neu, Ihc
FDA Pre-Market Approval
FDA Class 3
·INSITE HER-2/NEU KIT
System, Test, Her-2/Neu, Ihc
FDA Pre-Market Approval
FDA Class 3
·PPATHWAY Anti-HER-2/NEU (4B5) Rabbit Monoclonal Primary Antibody
Sentosa SQ Virus Testing Solutions (4x24)
FDA UDI
VELA OPERATIONS SINGAPORE PTE. LTD.·08885013956559·The Sentosa SQ HIV-1 Genotyping Assay is a next...
Sentosa SQ HIV-1 Positive Control Kit (8)
FDA UDI
VELA OPERATIONS SINGAPORE PTE. LTD.·08885013956597·The Sentosa SQ HIV-1 Genotyping Assay is a next...
Sentosa SQ HIV-1 Genotyping Reagents (4x24)
FDA UDI
VELA OPERATIONS SINGAPORE PTE. LTD.·08885013956542·The Sentosa SQ HIV-1 Genotyping Assay is a next...
Sentosa SQ HIV-1 Positive Control Kit (96)
FDA UDI
VELA OPERATIONS SINGAPORE PTE. LTD.·08885013956566·The Sentosa SQ HIV-1 Genotyping Assay is a next...
C6-2GU Ultrasonic Probe(FDA)
FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904092768·
VENTANA HER2 DISH DNA PRB CKT-US Export
FDA registration
VENTANA MEDICAL SYSTEMS, INC.·1 product·🇺🇸 United States
INFORM HER2 Dual ISH DNA Probe Cocktail
FDA registration
VENTANA MEDICAL SYSTEMS, INC.·1 product·🇺🇸 United States
VENTANA HER2 Dual ISH DNA Probe Cocktail
FDA registration
VENTANA MEDICAL SYSTEMS, INC.·1 product·🇺🇸 United States
BAYER IMMUNO 1 HER-2/NEU ASSAY
FDA 510(k)
FDA Class 2
·Immunology
BAYER ADVIA CENTAUR HER-2/NEU ASSAY
FDA 510(k)
FDA Class 2
·Immunology
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DYNAGEN EL ICD, DYNAGEN MINI ICD, INOGEN EL ICD, INOGEN MINI ICD, ORIGEN EL ICD, ORIGEN MINI ICD
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DYNAGEN CRT-D, DYNAGEN X4 CRT-D, INOGEN CRT-D, INOGEN X4 CRT-D, ORIGEN CRT-D, ORIGEN X4 CRT-D
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·NG3 CARDIAC RESYNCHRONIZATION THERAPY-DEFIBRILLATOR (CRT-D),DYNAGEN CRT-D,DYNAGEN X4 CRT-D,INOGEN CRT-D,INOGEN X4 CRT-D,
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·NG3 IMPLANTABLE CARDIOVERTER DEFIBRILLATOR, DYNAGEN EL ICD, DYNAGEN MINI ICD, INOGEN EL ICD, INOGEN MINI ICD,ORIGEN EL
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·NG3 FAMILY OF ICD'S (ORIGEN, INOGEN, & DYNAGEN); PROGENY FAMILY OF ICD'S (INCEPTA, ENERGEN, & PUNCTUA)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·NG3 FAMILY OF CRT-D'S (ORIGEN, INOGEN, & DYNAGEN); PROGENY FAMILY OF CRT-D'S (INCEPTA, ENERGEN, & PUNCTUA)
TBR Zirconnect
FDA registration
SUDIMPLANT SA·2 products·🇫🇷 France