2,348 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC MODEL 2090 BURBOT AND SPLAKE PROGRAMMERS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CHORUS DDD PACEMAKER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DDD PULSE GENERATOR 674
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VIGOR DDD PACEMAKER SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·META DDD MODEL 1230 PACER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·META DDD MODEL 1230 PACER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CETA DDD MODEL 1230 PACER
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·META DDD MODEL 1230 PACER
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·META DDD MODEL 1230 PACER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK AV DDD/AV II DDDD
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA PACEMAKER SYS; VIGOR DDD MODEL 950
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AUTIMA PACING SYSTEM (META DDD MODEL 1230)
TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS/TRANSVENOUS, PERMANENT SCREW-IN PACING LEADS
FDA 510(k)
FDA Class 3
·Cardiovascular
MODEL 2188 CORONARY SINUS LEAD.
FDA 510(k)
FDA Class 3
·Cardiovascular
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODEL 6291,2,6 & META DDD MODEL 1230
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF IQ RESTORE +3.0D ADD POWER INTRAOCULAR LENS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DELTA PACEMAKER SYSTRM; VIGOR DDD MODEL 950 (MASTER)
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
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF IQ RESTOR +3.0D ADD POWER POSTERIOR CHAMBER IOLS