1,032 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Stimulator, Electrical, Implantable, For Incontinence
FDA Pre-Market Approval
FDA Class 3
·InterStim Therapy System, Verify Evaluation System
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·Activa Deep Brain Stimulation Therapy System
Implanted Electrical Device Intended For Treatment Of Fecal Incontinence
FDA Pre-Market Approval
FDA Class 3
·InterStim THerapy System, Verify Evaluation System
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Master Restore, Itrel, Synergy and Intellis; Spinal Cord Stimulation Systems and Pisces, Specify, and Vectris Spinal Cor
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 2920 (PRM) SYSTEM ZOOM (DELTA PACEMAKER SYSTEM)
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·LATITUDE INDUCTIVE COMMUNICATOR ; LATITUDE PROGRAMMER/RECORDER/MONITOR (PRM)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 2920 (PRM) SYSTEM ZOOM (VENTAK AV AICD SYSTEM)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 2920 PRM SYSTEM ZOOM (VENTAK PRX AICD SYSTEM)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 2920 (PRM) SYSTEM ZOOM (VIGOR DR/SR PACEMAKER SYSTEM)
PD-1400 PACER/DEFIBRILLATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·MODEL 3140 ZOOM WIRELESS TRANSMITTER AND MODEL 3120 ZOOM LATITUDE PROGRAMMER/RECORDER/MONITOR (PRM)
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·STAARVISC II & SHELLGEL SODIUM HYAURONATE
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Programmer Recorder Monitor (PRM) for Implantable Pulse Generators, Model 3300 LATITUDE Programming System, Model 6395 I
Lymph Node Location System During Sentinel Biopsy Procedure
FDA Pre-Market Approval
FDA Class 3
·Magtrace/and Sentimag Magnetic Localization System
Lymph Node Location System During Sentinel Biopsy Procedure
FDA Pre-Market Approval
FDA Class 3
·Magtrace and Sentimag Magnetic Localization System
Neuromodulator For Obesity
FDA Pre-Market Approval
FDA Class 3
·MAESTRO RECHARGEABLE SYSTEM
Neuromodulator For Obesity
FDA Pre-Market Approval
FDA Class 3
·Maestro Rechargeable System
Neuromodulator For Obesity
FDA Pre-Market Approval
FDA Class 3
·Maestro Rechargeable System
Neuromodulator For Obesity
FDA Pre-Market Approval
FDA Class 3
·MAESTRO RECHARGEABLE SYSTEM
Lymph Node Location System During Sentinel Biopsy Procedure
FDA Pre-Market Approval
FDA Class 3
·MagtraceTM and Sentimag(R) Magnetic Locatization System