176 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Senza Spinal Cord Stimulation (SCS) System and HFX iQ System
Kit, Assay, Progesterone Receptor
FDA Pre-Market Approval
FDA Class 3
·PGR-EIA MONOCLONAL
Kit, Assay, Progesterone Receptor
FDA Pre-Market Approval
FDA Class 3
·ABBOTT PGR-EIA MONOCLONAL
Kit, Assay, Progesterone Receptor
FDA Pre-Market Approval
FDA Class 3
·ABBOTT PGR-EIA MONOCLONAL
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·ADVANTIO, INGENIO, VITALIO, FORMIO PGS
System, Hemodynamic, Implantable
FDA Pre-Market Approval
FDA Class 3
·CardioMEMS HF System
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·CONTAK RENEWAL TR FAMILY OF PULSE GENERATORS (PGS)
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
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
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EMBLEM S-ICD Pulse Generator (PG) & MRI S-ICD Pulse Generator (PG) (S-ICD's)
Implanted Brain Stimulator For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NEUROPACE RNS SYSTEM
Implanted Brain Stimulator For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NeuroPace RNS System
Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification
FDA Pre-Market Approval
FDA Class 3
·Nucleus® Hybrid L24 Cochlear Implant System
Implanted Brain Stimulator For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NeuroPace RNS System
Implanted Brain Stimulator For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NEUROPACE RNS SYSTEM
Implanted Brain Stimulator For Epilepsy
FDA Pre-Market Approval
FDA Class 3
·NeuroPace RNS System
Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification
FDA Pre-Market Approval
FDA Class 3
·Nucleus® Hybrid L24 Cochlear Implant System