3,082 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CHORUS(R) MODEL 6001,3,33 DDD MODEL CPRI MODEL P2A
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·OCUSIL(R) (NEFOCON A) CONTACT LENSES ADD FIN LABS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CHORUS(R) MODEL 6004&6034 DDD MODEL CPRI MODEL P2A
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·CHIROFLEX(TM) ADD MODEL 32-C11XX SINGLE PIECE IOL
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF IQ RESTOR IOLS 3.0 AND 4.0 D ADD POWERS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODELS 940 & 941 VISTA DDD GEN. & MODEL 2050 MODUL
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF IQ RESTOR IOLS +3.0 D & +4.0 D ADD POWERS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VISTA DDD MODEL 942 & 944 AND SOFTWARE MODULE MODEL 2052
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 446 & 447 VISTA T,MODEL 940 & 941 VISTA DDD
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 446 & 447 VISTA T,MODEL 940 & 941 VISTA DDD