BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    iFuse Implant System® - iFuse-3D implant

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TOMAS PIN SD 6, 8, AND 10 MM

    FDA 510(k)
    FDA Class 2 ·Dental

    VISION-SCIENCES ENT-5000 VIDEO ENT SCOPE WITH ENDOSHEATH TECHNOLOGY, VISION-SCIENCES DPU-5000/DPU-5050 VIDEO PROCESSOR

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 36 SIZE M 0

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 6, 2021

    PURITAN BENNETT 980 SERIES VENTILATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC/COVIDIEN·Product code CBK·September 17, 2025

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·June 11, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 14, 2011

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 8, 2008

    RHYTHMIA HDX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025

    UNSPECIFIED HA FILLER

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·February 13, 2020

    UNSPECIFIED PLLA FILLER

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·February 13, 2020

    UNSPECIFIED PLLA FILLER

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·February 13, 2020