BEUDAMED
    14 results · 19ms · Sources: EU EUDAMED, US FDA

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    HEMO-ALERT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDLINE ANGIOGRAPHIC CONTROL SYRINGE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    3-DAY BIOINDICATOR RELEASE PROCESS FOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TPRLC 133 MP TYPE1 PPS HO 20.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 9, 2018

    CER OPTION TYPE 1 TPR SLEVE -6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 9, 2018

    COOK FILTER CELECT UNI

    FDA Adverse Event
    Injury ·COOK MEDICAL·Product code DTK·June 18, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·January 2, 2013

    SERFAS ENERGY SUPER 90-S

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·November 1, 2010

    CER OPTION TYPE 1 TPR SLEVE -6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 8, 2018

    TPRLC 133 MP TYPE1 PPS HO 20.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 8, 2018

    G7 PPS LTD ACET SHELL 62H

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·August 8, 2018

    G7 NEUTRAL E1 LINER 36MM H

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·August 8, 2018

    S1S HIP HEAD CEMENT MOLD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWL·August 9, 2018

    HIP MOLD STEM W/REINF 13X145

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWL·August 9, 2018