BEUDAMED
    2,829 results · 31ms · Sources: EU EUDAMED, US FDA

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    LINK(R) MP(R) STEM

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDI·August 1, 2011

    LINK(R) MP(R) STEM

    FDA Adverse Event
    Injury ·WALDEMAR LINK GMBH & CO. KG·Product code JDI·May 6, 2011

    LINK(R) MP(R) NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDI·May 3, 2011

    LINK(R) MP(R) NECK

    FDA Adverse Event
    Injury ·WALDEMAR LINK GMBH & CO. KG·Product code KWA·May 6, 2011

    ADULT MPR W/ ADULT MASK, AND RESERVOIR BAG

    FDA Adverse Event
    Death ·UNOMEDICAL S.A. DE C.V.·Product code BTM·November 16, 2011

    Resp-O2 Pediatric Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Bag

    FDA UDI
    Dynarex Corporation·00840117308350·Oxygen Tubing

    RespO2 Pediatric Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Bag Oxygen

    FDA UDI
    Dynarex Corporation·00840117326002·Tubing, Peep Valve

    ORTHOPILOT THA REAMER SHANK MPR HARRIS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code HAW·April 29, 2021

    LINK(R) MP(R) FIXATION SCREW

    FDA Adverse Event
    Injury ·WALDEMAR LINK GMBH & CO. KG·Product code KWA·May 6, 2011

    LINK(R) MP(R) METAL SPACER

    FDA Adverse Event
    Injury ·WALDEMAR LINK GMBH & CO. KG·Product code HRS·May 6, 2011

    Resp-O2 Pediatric Manual Pulmonary Resuscitatir (MPR)Mask,Reservoir Bag Oxygen

    FDA UDI
    Dynarex Corporation·00840117313958·Tubing

    Resp-O2 Adult Manual Pulmonary Resuscitator(MPR) Mask, Reservoir Tubing Oxygen

    FDA UDI
    Dynarex Corporation·00840117308374·Tubing

    Resp-O2 Adult Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Bag Oxygen

    FDA UDI
    Dynarex Corporation·00840117313934·Oxygen Tubing, PEEP Valve

    Resp-O2 Infant Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Tubing Oxygen

    FDA UDI
    Dynarex Corporation·00840117313972·Tubing

    Resp-O2 Infant Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Bag Oxygen

    FDA UDI
    Dynarex Corporation·00840117308336·Tubing

    NEUROVENT-P

    FDA Adverse Event
    Malfunction ·RAUMEDIC AG·Product code GWM·December 19, 2017

    CANON AQUILION ONE

    FDA Adverse Event
    Malfunction ·CANON MEDICAL SYSTEM, USA, INC.·Product code JAK·November 16, 2022

    INTELEPACS

    FDA Adverse Event
    Malfunction ·INTELERAD MEDICAL SYSTEMS INC.·Product code LLZ·December 16, 2021

    GORE TAG THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·November 15, 2012

    UNK REAMER

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HTO·December 29, 2022