BEUDAMED
    129 results · 38ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM(R)

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND II SYSTEM

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM(R)

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM(R)

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM

    Stimulator, Neuromuscular, Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCONTROL FREEHAND SYSTEM

    HydraLok

    FDA UDI
    Choice Spine, LP·10885862129338·

    KENAFLEXX

    FDA UDI
    KENTRON HEALTHCARE, INC.·00852244007884·35" IV EXTENSION SET WITH FEMALE LUER AND ROTAT...

    DragonFly™ BUR, TROCAR PERF, 95MM L, 0.35MM Ø

    FDA UDI
    Grace Medical, Inc.·00844505009904·DragonFly™ TROCAR PERFORATOR BUR 95MM LENGTH, 0...

    Elite®

    FDA UDI
    Ortho Organizers, Inc.·00190707052164·.018 SAA U7R ROTH BUCCAL TUBE

    SURGIFLATOR 20

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SELOX SR 53

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code LWS·June 14, 2006

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·December 3, 2017

    Leadless Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·Aveir VR Leadless System

    Stimulator, Invasive Bone Growth

    FDA Pre-Market Approval
    FDA Class 3 ·SpF® Implantable Spinal Fusion Stimulator