33 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·COLLAMER UV-ABSORBING POSTERIOR CHAMBER IOL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SILICON UV-ABSORBING POSTERIOR CHAMBER IOL
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Telemetry Wand
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device
Pulmonary Stent
FDA Pre-Market Approval
FDA Class 3
·PALMAZ MULLINS XD Pulmonary Stent
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device (ACD)
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device - Model Number BAR-A8-8MM (2730815-A&), Barricaid® Annular Closure Device - Model Numb
Pulmonary Stent
FDA Pre-Market Approval
FDA Class 3
·PALMAZ MULLINS XD Pulmonary Stent
Pulmonary Stent
FDA Pre-Market Approval
FDA Class 3
·PALMAZ MULLINS XD Pulmonary Stent
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·BARRICAID ANULAR CLOSURE DEVICE (ACD)
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Annular Closure Device