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

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    Filters Status: Injury ×

    UNIDENTIFIED SIGMA PARTIAL GCK

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code JWH·May 14, 2013

    GCK UNI TIB TRAY CEM SZ3 LM/RL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC., DIVISION: DEPUY-RAYNHAM·Product code HRY·June 23, 2008

    EVIS EXERA II GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·November 30, 2016

    EVIS EXERA II GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·November 30, 2016

    EVIS EXERA II GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·November 30, 2016

    EVIS EXERA II GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·November 30, 2016

    EVIS EXERA II GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·November 30, 2016

    OLYMPUS EVIS EXERA II GASTROVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GCK·May 22, 2012

    OLYMPUS EVIS EXERA GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code GCK·June 12, 2013

    OLYMPUS

    FDA Adverse Event
    Injury ·OLYMPUS OPTICAL CO. LTD.·Product code GCK·March 1, 2007

    OLYMPUS

    FDA Adverse Event
    Injury ·OLYMPUS OPTICAL CO. LTD.·Product code GCK·November 11, 2005

    PENTAX

    FDA Adverse Event
    Injury ·ASAHI OPTICAL CO., LTD.·Product code GCK·May 15, 2002

    SURGIPLAS IMPLEO GEL TEXTURED MAMMARY PROSTHESIS EXTRA HIGH RANGE EHR 520

    FDA Adverse Event
    Injury ·GC AESTHETICS (GCA)·Product code FTR·April 14, 2026

    SURGIPLAS IMPLEO GEL TEXTURED MAMMARY PROSTHESIS EXTRA HIGH RANGE EHR 520

    FDA Adverse Event
    Injury ·GC AESTHETICS (GCA)·Product code FTR·April 14, 2026

    UNK DERMAL FILLER

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURER·Product code LMH·June 29, 2022

    CYPHER CLINICAL 3.00 X 18MM

    FDA Adverse Event
    Injury ·CORDIS RODEN·Product code NIQ·July 13, 2006

    CYPHER CLINICAL 3.0 X 23MM

    FDA Adverse Event
    Injury ·CORDIS RODEN·Product code NIQ·July 28, 2006

    CYPHER CLINICAL 2.50 X 8MM

    FDA Adverse Event
    Injury ·CORDIS RODEN·Product code NIQ·July 28, 2006

    ORIDION

    FDA Adverse Event
    Injury ·COVIDIEN·Product code CCK·September 10, 2015

    PEDI-CAP

    FDA Adverse Event
    Injury ·NELLCOR·Product code CCK·May 6, 2014