BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    STRYKER WEDGE SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BCI WW1030 PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endoskeleton® TA Interbody Fusion Device, Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TO Interbody Fusion Device, Endoskeleton® TT Interbody Fusion Device, Endoskeleton® TC Interbody Fusion Device, Endoskeleton® TCS Interbody Fusion Device, Endoskeleton® TL Interbody Fusion Device, Endoskeleton® TA Vertebral Body Replacement (VBR) Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·November 7, 2019

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 28, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 6, 2014

    CRYOVALVE SG

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MIE·February 10, 2011