688 results
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19ms
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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
·VITATRON DA+C & VITATRON DA+T SERIES IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA+C & VITATRON DA+T SERIES IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA+ C SERIES & VITATRO DA+ T SERIES IPG
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·Activa® Deep Brain Stimulation Therapy System, Percept PC BrainSense
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·ENRHYTHM
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAXIMO II, SECURA AND VIRTUOSO II
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CONCERTO II, CONSULTA AND MAXIMO II
System, Laser, Photodynamic Therapy
FDA Pre-Market Approval
FDA Class 3
·600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CLARITY /VITATRON DA+ C-SERIES/DIAMOND 3/JADE 3/RUBY 3/VITATRON DA+ T-SERIES/TOPAZ 3/VITA 2/VITA IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CLARITY/VITATRON DA+C-SERIES/DIAMOND 3/JADE 3/RUBY 3/VITATRON DA+T-SERIES/TOPAZ 3/VITA 2/VITA IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CLARITY/DA+ C-SERIES/T-SERIES/DIAMOND 3/II/JADE 3/II/RUBY 3/II/SELECTION AFM/TOPAZ 3/II/VITA/2
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CLARITY/DA+C & T SERIES/DIAMOND 3/II/JADE 3/II/RUBY 3/II/ SELECTION AFM/TOPAZ 3/II/VITA/VITA 2
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·BRAVA,BRAVA QUAD,CONCERTO II,CONSULTA,MAXIMO II,PROTECTA,PROTECTA XT,VIVA QUAD S, VIVA QUAD XT,VIVA S, VIVA XT CRT-DS, C
POWRPAK REPLACEMENT BATTERIES FOR PHISIO-CONTROL LIFEPAK 5/10
FDA 510(k)
FDA Class 3
·Cardiovascular
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL AORTIC BIOPROSTHESIS
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL AORTIC BIOPROSTHESIS; THEON PERICARDIAL AORTIC BIOPROSTHESIS WITH THERMALFIX TI
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·Mosaic Porcine Bioprosthesis
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS(R) BIOPROSTHESIS, MODELS 2625 AND 6625
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER- EDWARDS PORCINE BIOPROSTHESIS
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER EDWARDS BIOPROSTHESIS