10,000 results
·
49ms
·
Sources: EU EUDAMED, US FDA
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00812345027457·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00812345027426·Cardiology Information System Workstation
Scribe
FDA UDI
MORTARA INSTRUMENT, INC.·00817655020457·Cardiology Information System Workstation
Scribe
FDA UDI
MORTARA INSTRUMENT, INC.·00817655020587·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00817655022376·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00817655022369·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00817655022437·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00817655022383·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00817655022413·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00812345027433·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00812345027464·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00817655022390·Cardiology Information System Workstation
Modality Manager
FDA UDI
MORTARA INSTRUMENT, INC.·00812345027440·Cardiology Information System Workstation
Powder Free Nitrile Examination Gloves Tested For Use With Chemotherapy Drugs
FDA 510(k)
FDA Class 1
·General Hospital
Implanted Phrenic Nerve Stimulator For Central Sleep Apnea
FDA Pre-Market Approval
FDA Class 3
·remede System
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented
FDA Pre-Market Approval
FDA Class 3
·CERAMAX Ceramic Hip System
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·LCS Total Knee System
System, Test, Her-2/Neu, Nucleic Acid Or Serum
FDA Pre-Market Approval
FDA Class 3
·PATH VYSION HER-2 DNA PROBE KIT
Fluorescence In Situ Hybridization, Anaplastic Lymphoma Kinase, Gene Rearrangement
FDA Pre-Market Approval
FDA Class 3
·VYSIS ALK BREAK APART FISH PROBE KIT
ALTHEA
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·OFF CARR Srl·12 devices