BEUDAMED
    23 results · 27ms · Sources: EU EUDAMED, US FDA

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    MEGA POWER ELECTROSURGICAL GENERATOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TEMPO AQUA ANGIOGRAPHIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STENT SUPPORT GUIDE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    S4C POLYAXIAL SCREW 3.5X12MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code MNI·May 1, 2009

    BIPAP AUTO M-SERIES

    FDA Adverse Event
    Death ·RESPIRONICS, INC·Product code BZD·July 11, 2012

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 14, 2022

    BIPAP AUTO BIFLEX

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 14, 2022

    BIPAP AUTO SERIES ASSY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 31, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 14, 2022

    BIPAP AUTO SERIES ASSY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code BZD·March 31, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    OXF ANAT BRG LT SM SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·June 14, 2018

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 31, 2022

    OXFORD CEMENTLESS TIBIA C LM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·June 14, 2018

    CORAIL AMT COLLAR SIZE 13

    FDA Adverse Event
    Injury ·DEPUY FRANCE·Product code KWA·April 10, 2013

    ADAPTER NUT

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·March 15, 2011

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008