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

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    EF1

    FDA Adverse Event
    Malfunction ·MEDSHAPE, INC.·Product code KTT·September 23, 2025

    6000036-1999-00169

    FDA Adverse Event
    Malfunction ·December 28, 1999

    6000036-1999-00175

    FDA Adverse Event
    Malfunction ·December 28, 1999

    6000036-1999-00174

    FDA Adverse Event
    Malfunction ·December 28, 1999

    COATED VICRYL PLUS (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAM·February 3, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 11, 2014

    TITANIUM GREENFIELD VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·MEDI-TECH / A DIV OF BOSTON SCIENTIFIC CORP.·Product code DTK·September 19, 2000

    TITANIUM GREENFIELD VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code DTK·October 25, 1999

    TITANIUM GREENFIELD VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·MEDI-TECH A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code DTK·October 25, 1999

    TITANIUM GREENFIELD VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·MEDI-TECH / A DIV OF BOSTON SCIENTIFIC CORP.·Product code DTK·September 19, 2000

    XXL BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MEDI-TECH / A DIVISION OF BOSTON SCIENTIFIC CORP·Product code LIT·December 9, 1999

    TITANIUM GREENFIELD VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·MEDI-TECH A DIV. OF BOSTON SCIENTIFIC CORP.·Product code DTK·April 7, 1998

    TITANIUM GREENFIELD VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·MEDI-TECH A DIV. OF BOSTON SCIENTIFIC CORP.·Product code DTK·April 7, 1998