BEUDAMED
    20 results · 23ms · Sources: EU EUDAMED, US FDA

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    IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    ADVANCE UNICONDYLAR KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SCIMED CARDIOTHERM CARDIOPLEGIA DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DELTA CER HEAD 12/14 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code LZO·October 30, 2012

    DELTA CER HEAD 12/14 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code LZO·October 30, 2012

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 30, 2012

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code JDI·November 14, 2011

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 14, 2011

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·September 26, 2012

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·September 26, 2012

    ZERO TIP NITINOL STONE RETRIEVAL BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFL·December 3, 2010

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code PAH·July 3, 2014

    36CM PERM CATH KIT X5

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code LFJ·December 7, 2012

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·September 26, 2012

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 25, 2012

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 25, 2012

    SUMMIT POR TAPER SZ8 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 25, 2012

    SUMMIT POR TAPER SZ6 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code LPH·April 9, 2015

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 30, 2012

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·September 26, 2012