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

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    DRI-VENT ARTERIAL BLOOD SAMPLING KIT

    FDA 510(k)
    FDA Unclassified ·Unknown

    VANGUARD 360 DISTAL FEMORAL AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 9, 2019

    VANGUARD 360 DST FEMORAL AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 9, 2019

    VANGUARD 360 UNIVERSAL POSTERIOR FEMORAL AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 9, 2019

    VANGUARD SSK 360 RIGHT FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 9, 2019

    BIOMET 360 TIBIAL 5.0 OFFSET ADAPTER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 9, 2019

    MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MEDELA NAMUAL BREAST PUMP

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    TOTAL CARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·February 13, 2014

    STERRAD EQUIPMENT (MLR)

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·October 27, 2010

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·November 15, 2012

    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 125 MM, Silicone, Sterile, Item 431190.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020