33 results · 18ms · Sources: EU EUDAMED, US FDA

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