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

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    Filters FDA Adverse Event ×

    HEARTSTREAM FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 25, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 13, 2011

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATOIN·Product code GZB·July 17, 2014

    G7 PPS LTD ACET SHELL 48C

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 30, 2019

    BONE SCR 6.5X35 SELF-TAP

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code MRA·May 30, 2019

    FEMORAL STEM 12/14 NECK TAPER PLASMA SPRAYED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·May 30, 2019

    BONE SCR 6.5X25 SELF-TAP

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code MRA·May 30, 2019

    ACT ARTIC HD ARCOM XL 28X38MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 30, 2019

    G7 DUAL MOBILITY LINER 38MM C

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 30, 2019

    ACT ARTIC HD ARCOM XL 28X38MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 30, 2019