BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    LMI OCCLUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221117663·3M™ Victory Series™ Second Molar Bands, 955-125...

    PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GUARANTY HAIR REMOVAL SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·August 2, 2012

    SENSOR MODULE LEVEL/BUBBLE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·May 11, 2012

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·February 11, 2013

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 24, 2014

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·January 6, 2012

    S5 BUBBLE DETECTOR SENSOR 3/16''

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code KRL·February 25, 2022

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·January 6, 2012