BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 8, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 17, 2012

    SYNERGY

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 12, 2010

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·December 22, 2011

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·May 23, 2013

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·May 10, 2012

    TRITANIUM REVISION ACETABULAR

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·September 26, 2014

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·September 6, 2023

    COBAS 4800 HPV TEST

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS·Product code MAQ·July 17, 2017

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·May 10, 2012