BEUDAMED
    5 results · 28ms · Sources: EU EUDAMED, US FDA

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    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code DXC·June 23, 2006

    PFC SIGMA STAB+ INS 10MM SZ2

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·November 30, 2017

    CLYDESDALE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·August 4, 2015

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 22, 2010

    12/14 ARTICUL 40MM M SPEC+5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code LPH·July 29, 2014