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

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    Q.I.C. BLEEDING TIME DEVICE

    FDA 510(k)
    FDA Class 2 ·Hematology

    MODIFICATION TO: STOCKERT S5 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DYNATRON 406 ELECTROTHERAPY APPARATUS

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

    S5 SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

    S5 SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

    S5 SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

    S5 SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

    S5 SENSOR MODULE FOR BUBBLE DETECTOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·June 13, 2014

    R3

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·December 13, 2012

    UNKNOWN DEPUY BONE CEMENT

    FDA Adverse Event
    Injury ·DEPUY CMW 9610921·Product code LOD·June 26, 2015

    LCD TOUCHSCREEN, RP150, S5

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 14, 2012

    LCD TOUCHSCREEN, RP150, S5

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 15, 2012

    S5 SINGLE ROLLER PUMP

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 21, 2010

    S5 ROLLER PUMP

    FDA Adverse Event
    Malfunction ·Product code DTQ·April 11, 2011