BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    OPUS SPEEDLOCK KNOTLESS FIXATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450210406·

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0106150·Trial, 26 x 15mm, 8 Degree, Tapered, Straight

    SYRINGE 0.5ML 31GA 8MM

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 19, 2021

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962108789·PROBE, 6", DOUBLE ENDED, SLIVER

    SUPER SECUR-FIT HA HIP STEMS AND SUPER SECUR-FIT PLUS HA HIP STEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CYCLOTEC AMT CTI TENS DEVICE

    FDA 510(k)
    FDA Class 2 ·Neurology

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·December 29, 2015

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·May 2, 2013

    ELECTRIC PEN DRIVE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·September 15, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 26, 2011