1,869 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS DURAFLEX LOW PRESSURE BIOPROTHESIS
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDEARDS DURAFLEX LOW PRESSURE PROCINE MITRAL BIOPROSTHESIS
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL BIOPROSTHESIS
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·ADX PULSE GENERATOR
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS DURAFLEX LOW PRESSURE, PORCINBE MITRAL BIOPROSTHESIS
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Tendril MRI leads (MRI)
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·PSW 1802.U, ACTROS, AXOS, BA03, CYLOS, DROMOS, KAIROS, PHILOS, PHILOS II, PROTOS, EVIA, ENTOVIS, ECURO, EFFECTA, ESTELLA
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS DURAFLEX LOW PRESSURE BIOPROSTHESIS MODELS 6625LP AND 6625-ESR-LP
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Assurity, Assurity +, Endurity, Accent and Victory XL
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Edora / Enitra /Enticos / Evity PSW 1701.U
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·Mosaic Bioprosthesis and Mosaic Ultra Bioprosthesis
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·Hancock II Bioprosthesis
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·HANCOCK LOW POROSITY VALVED CONDUIT
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL BIOPROSTHESES
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·P880086 Endurity PM1162, PM2162; Endurity Core PM1140, PM2140; AV Plus Dx Lead 1368; Verity ADx XL 5357M/S, 5356, 5256,
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·PSW 2301.U, NEO 2301.U
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·SENSOLOG(R) CARDIAC PACING SYSTEM
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS DURAFLEX LOW PRESSURE BIOPROSTHESIS MODELS 6625LP AND 6625-ESR-LP
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MODEL 3037A FUNCTION PACK
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·Carpentier-Edwards PERIMOUNT Theon Pericardial Aortic Bioprosthesis with ThermaFix tissue process, Carpentier-Edwards PE