17 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·INSPIRIS RESILIA Aortic Valve, MITRIS RESILIA Mitral Valve
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·SAPIEN 3 Ultra RESILIA Transcatheter Heart Valve
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·GFX 2 OVER-THE-WIRE CORONARY STSENT SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·GFX & MICRO STENT II OVER-THE-WIRE CORONARY STENT SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT TM II, MICRO STENT TM II XL, GFX TM, GFX TM XL
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT TM II, MICRO STENT TM II XL, GFX TM, GFX TM XL
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·GFX-XP/GFX2 CORONARY STENT SYSTEM
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·Edwards Pericardial Aortic Bioprosthesis, Edwards Pericardial Mitral Bioprosthesis, INSPIRIS RESILIA Aortic Valve, KONEC
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·GFX OVER-THE-WIRE CORONARY STENT SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·GFX SL OVER-THE-WIRE CORONARY STENT SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT II & GFX OVER-THE-WIRE CORONARY STENT SYSTEMS
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT II & GFX OVER-THE-WIRE CORONARY STENT SYSTEMS
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·Edwards Pericardial Aortic Bioprosthesis and INSPIRIS RESILIA Aortic Valve
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT II OVER-THE-WIRE CORONARY STENT SYSTEM;GFX OVER-THE-WIRE CORONARY STENT SYSTEM
Processor, Cervical Cytology Slide, Automated
FDA Pre-Market Approval
FDA Class 3
·BD PREPSTAIN SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·AVE MICRO STENT II OVER-THE-WIRE CORONARY STENT SYSTEM AND AVE GFX OVER-THE-WIRE CORONARY STENT SYSTEM
Processor, Cervical Cytology Slide, Automated
FDA Pre-Market Approval
FDA Class 3
·PREPSTAIN INSTRUMENT