BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    Agnes

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

    ARSTASIS ACCESS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    20.1 INCH (51 CM) COLOR LCD MONITOR CCL208 (CDL2013A)

    FDA 510(k)
    FDA Class 2 ·Radiology

    ARSTASIS ACCESS SYSTEM

    FDA Adverse Event
    Other ·ARSTASIS INC.·Product code DYB·November 15, 2010

    ARSTASIS ACCESS SYSTEM

    FDA Adverse Event
    Malfunction ·ARSTASIS, INC.·Product code DYB·November 19, 2010

    ARSTASIS ACCESS SYSTEM

    FDA Adverse Event
    Other ·ARSTASIS, INC.·Product code DYB·November 22, 2010

    ARSTASIS ACCESS SYSTEM

    FDA Adverse Event
    Injury ·ARSTASIS, INC.·Product code DYB·November 1, 2010

    LIFEVEST WCD 4000 SYS

    FDA Adverse Event
    Death ·ZOLL MANUFACTURING CORPORATION·Product code MVK·October 9, 2014

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD.·Product code HQL·June 25, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 20, 2011

    DURASULA CONSTRAINED INSERT SIZE 38MM/65MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWZ·August 12, 2020

    NEUTRAL NECK USE WITH 12/14 TAPER STEMS ONLY 28

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 12, 2020

    METASULA STANDARD INSERT SIZE 28MM X 65MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 12, 2020