BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    APEX-DL Spine System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFESHIELD VISION INFUSION SET WITH PRE-PIERCED RESEAL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IMMULITE/IMMULITE 1000 PROGESTERONE CALIBRATION VERIFICATION (CVM)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    FUJIFILM DOUBLE BALLOON ENDOSCOPES EN-450T5/W

    FDA Adverse Event
    Death ·FUJIFILM CORPORATION·Product code FDA·January 26, 2024

    EXTENSION SET WITH T-CONN. SL

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·October 3, 2013

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 3, 2013

    SYNCHRON® SYSTEMS RHEUMATOID FACTOR (RF) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·June 29, 2011

    ACUVUE OASYS

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·August 29, 2008

    BD SAFE-CLIP¿ NEEDLE CLIPPING & STORAGE DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·September 25, 2019

    SHARPS DISPOSAL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·August 16, 2019