BEUDAMED
    15 results · 39ms · Sources: EU EUDAMED, US FDA

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    FOGARTY ARTERIAL CATHETER

    FDA Adverse Event
    EDWARDS CVS DIV. BAXTER HEALTHCARE CORP.·Product code DXE·December 23, 1993

    SMR GLENOID PEG TT SMALL-R #L

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·March 18, 2022

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·March 12, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·February 18, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·February 19, 2008

    M2A 38MM MODULAR HEAD STD NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·March 5, 2012

    TECNIS ODYSSEY TORIC II IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code MFK·January 22, 2026

    TAPERLOC MODULAR FEMORAL 12.5MM X 145MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 5, 2012

    M2A 38 NON-FLARED ONE-PIECE CUP 50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 5, 2012

    M2A 38MM MODULAR HEAD COMPONENT STD NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 5, 2012

    BONE SCREW Ø6,5 H.25MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LPH·November 24, 2021

    TAPERLOC MODULAR FEMORAL 13.5MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 5, 2012

    M2A 38 NON-FLARED ONE-PIECE CUP 52MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 5, 2012

    SMR GLENOID PEG TT SMALL-R #L

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·October 28, 2021

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·March 11, 2022