BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    CO2 GAS WARMING UNIT (6-800-00)

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SMITH & NEPHEW ARTHROSCOPE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Varian Cervical Sleeves

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD VACUTAINER PPT PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 7, 2018

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·February 21, 2013

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 20, 2011

    ULTRA ICE INTRACARDIAC ECHO CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code ITX·July 25, 2014

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·July 17, 2018