50 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT ENDOPROTHESIS
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT ENDOPROTHESIS NATIVE CORONARY INDICATION
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT ENDOPROSTHESIS SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT ENDOPROSTHESIS
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT SELF-EXPANDING CORONARY STENT
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·SCIMED MAGIC WALLSTENT ENDOPROSTHESIS WITH DELIVERY SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT ENDOPROSTHESIS WITH DELIVERY SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·SCIMED MAGIC WALLSTENT ENDOPROSTHESIS WITH DELIVERY SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT(R) ENDOPROSTHESIS WITH DELIVERY SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT EDNDOPROSTHESIS AND RADIUS CORONARY STENT WITH DELIVERY SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT(R) SELF-EXPANDING CORONARY STENT
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT SELF-EXPANDING CORONARY STENT
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT ENDOPROSTHESIS
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MAGIC WALLSTENT SELF-EXPANDING CORONARY STENT
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980009·DeltaForm HighDefinition posterior; shade A1; s...
Computer-Assisted Personalized Sedation System
FDA Pre-Market Approval
FDA Class 3
·SEDASYS COMPUTER-ASSISTED PERSONALIZED SEDATION SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·BYREL PROGRAMABLE PACEMAKER
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code LPB·April 25, 2023
MAESTRO FOOT SWITCH
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018
MAESTRO 4000 CONTROLLER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025