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

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    Filters Status: Injury ×

    SOMRYST

    FDA Adverse Event
    Injury ·PEAR THERAPEUTICS, INC.·Product code QVO·October 11, 2023

    SCREW DVO DRIVE

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code LRZ·December 2, 1992

    CRYSTALENS

    FDA Adverse Event
    Injury ·EYEONICS, INC.·Product code HQL·October 17, 2006

    RAINDROP CORNEAL INLAY

    FDA Adverse Event
    Injury ·RVO 2.0, INC.·Product code LQE·May 23, 2024

    MAXIASPIRATOR

    FDA Adverse Event
    Injury ·EVO MEDICAL SOLUTIONS·Product code BTI·September 4, 2012

    RAINDROP INLAY

    FDA Adverse Event
    Injury ·RVO 2.0, INC.·Product code LQE·March 29, 2019

    CWIII ARTHROSCOPY PUMP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRX·April 28, 2023

    SKINVIVE BY JUVEDERM XC 2X1 ML

    FDA Adverse Event
    Injury ·ALLERGAN (PRINGY)·Product code LMH·October 31, 2023

    ONE PIECE MAIN PUMP&PATIENT EXT TBG

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRX·April 15, 2025

    K-LESS T-ROPE W/DRV, SYN REPR, TI

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HTN·August 8, 2024

    POWERWIRE RADIOFREQUENCY GUIDEWIRE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code PDU·May 8, 2019

    RAINDROP IMPLANT

    FDA Adverse Event
    Injury ·REVISION / RVO 2.0, INC.·Product code LQE·October 13, 2020

    RAINDROP UNDERLAY LENS

    FDA Adverse Event
    Injury ·REVISION / RVO 2.0, INC.·Product code LQE·October 21, 2019

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·January 29, 2024

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·January 29, 2024

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·January 29, 2024

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·January 29, 2024

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 24, 2025

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 24, 2025

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 24, 2025