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

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    Filters FDA Adverse Event ×

    250123/MONOJECT

    FDA Adverse Event
    Malfunction ·SHERWOOD·Product code FMI·July 1, 1993

    S-ROM*STM STD,36NK,14X09X130

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·November 12, 2014

    VICRYL (POLYGLACTIN 910) MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·November 20, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 15, 2011

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 26, 2013

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·May 16, 2014

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 16, 2014

    VISIGLIDE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code OCY·October 15, 2025