10,000 results
·
72ms
·
Sources: EU EUDAMED, US FDA
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·NIRFLEX PREMOUNTED CORONARY STENT SYSTEM
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLES 30 & 31 POSTERIOR CHAMBER IOLS
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
FDA Pre-Market Approval
FDA Class 3
·EXABLATE
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·EluNIR Ridaforolimus Eluting Coronary Stent System
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·BVI 1% OVD (1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID)
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·EluNIR Ridaforolimus Eluting Coronary Stent System
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·BIOLON 1% SODIUM HYALURONATE
Hybrid Stent Graft, Thoracic Aortic Lesion Treatment
FDA Pre-Market Approval
FDA Class 3
·Thoraflex Hybrid
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·EluNIR Ridaforolimus Eluting Coronary Stent System
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·NIRXCELL COCR CORONARY STENT ON RX SYSTEM (NIRXCELL STENT SYSTEM)
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·NIRXCELL COCR CORONARY STENT ON RX SYSTEM
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·BD 1% OVD (1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID)
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·EluNIR Ridaforolimus Eluting Coronary Stent System
Hybrid Stent Graft, Thoracic Aortic Lesion Treatment
FDA Pre-Market Approval
FDA Class 3
·Thoraflex Hybrid
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·BVI 1% OVD (1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID)
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLES 30 & 31 POSTERIOR CHAMBER IOLS
Hybrid Stent Graft, Thoracic Aortic Lesion Treatment
FDA Pre-Market Approval
FDA Class 3
·Thoraflex Hybrid
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·BIOLON 1% SODIUM HYALURONATE FOR OPHTHALMIC SURGERY
Laparoscopic Contraceptive Tubal Occlusion Device
FDA Pre-Market Approval
FDA Class 3
·FILSHIE CLIP (MARK VI) SYSTEM
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLES 30 & 31 POSTERIOR CHAMBER IOLS