399 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·QUIK-PAK Electrodes
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·QUIK-PAK Electrodes
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·QUIK-PAK Electrodes
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·samaritan® PAD 350P (SAM 350P), samaritan® PAD 360P (SAM 360P), samaritan® PAD 450P (SAM 450P), Pad-Paks (Adult, Pediatr
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·samaritan Public Access Automated External Defibrillators and Accessories
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartSine Technologies LLC's samaritan Public Access Automated External Defibrillators (SAM 350P, SAM 360P and SAM 450P)
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartSine Technologies LLC's samaritan Public Access Automated External Defibrillators (SAM 350P, SAM 360P and SAM 450P)
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartSine samaritan® Public Access Automated External Defibrillators and Accessories
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·CLARION CII BIONIC EAR SYSTEM (ADULT)
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·CLARION CII BIONIC EAR SYSTEM (PEDIATRIC)
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·Maestro 4000 Cardiac Ablation System (Controller, Remote and Pods)
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC IGM REAGENT PAK/CALIBRATOR
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·ZIMMER NEXGEN LPS-FLEX MOBILE/LPS-MOBILE BEARING KNEE SYSTEMS
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·Perceval PLUS Sutureless Heart Valve
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·BIOLECTRON ORTHO-PAK BONE GROWTH STIMULATOR/SPINALPAK SPINAL FUSION STIMULATOR
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·LIFEPAK CR® Plus Defibrillator, LIFEPAK EXPRESS® Defibrillator, and CHARGE-PAK® Battery Charger
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·BIOMET ORTHOPAK NON INVASIVE BONE GROWTH STIMULATOR SYSTEM; SPINAL PAK NON INVASIVE SPINE FUSION STIMULATOR SYSTEM
Device, Thermal Ablation, Endometrial
FDA Pre-Market Approval
FDA Class 3
·MICROSULIS MICROWAVE ENDOMETRIAL ABLATION (MEA) SYSTEM
Device, Thermal Ablation, Endometrial
FDA Pre-Market Approval
FDA Class 3
·MICROSULIS MICROWAVE ENDOMETERIAL ABLATION (MEA) SYSTEM
Device, Thermal Ablation, Endometrial
FDA Pre-Market Approval
FDA Class 3
·MICROSULIS MICROWAVE ENDOMETRIAL ABLATION (MEA) SYSTEM