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

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    Filters FDA Adverse Event ×

    M2A MAGNUM TPR ADPR TI

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·September 7, 2012

    RECAP SHELL COCR PC 54/48MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·September 7, 2012

    BI-METRIC HA/PC 11X135MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·September 7, 2012

    M2A MAGNUM MODULAR HD COCR 48MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·September 7, 2012

    E1 RINGLOC BIPOLAR SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 30, 2020

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 15, 2013

    TRIDENT 0 X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code LPH·February 16, 2011

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·February 26, 2008

    HEALONID GV

    FDA Adverse Event
    Injury ·PHARMACIA & UPJOHN, FYRISLUND·Product code LZP·January 14, 2002

    HEALONID GV

    FDA Adverse Event
    Injury ·PHARMACIA & UPJOHN, FYRISLUND·Product code MRE·January 14, 2002