BEUDAMED
    691 results · 42ms · Sources: EU EUDAMED, US FDA

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    BD 3ML LUER-LOK SYRINGE

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMF·July 16, 2012

    BEAVER-VISITEC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL INC·Product code HOZ·July 20, 2023

    BEAVER VISITEC

    FDA Adverse Event
    Injury ·BEAVER VISITEC INTERNATIONAL·Product code MDM·October 4, 2023

    BEAVER-VISITEC INTERNATIONAL, INC

    FDA Adverse Event
    Injury ·BEAVER-VISITEC INTERNATIONAL INC·Product code HQP·August 28, 2024

    BEAVER-VISITEC INTERNATIONAL INC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL INC·Product code HNN·July 19, 2024

    BEAVER-VISITEC INTERNATIONAL INC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL INC·Product code HMX·July 11, 2024

    BEAVER-VISITEC INTERNATIONAL INC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL INC·Product code HMX·April 29, 2024

    BEAVER-VISITEC INTERNATIONAL INC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL INC·Product code HNN·May 2, 2024

    BEAVER-VISITEC INTERNATIONAL INC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL INC·Product code HMX·June 17, 2024

    BEAVER-VISITEC INTERNATIONAL INC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL INC·Product code HMX·May 21, 2024

    ACCU-TEMP®

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HQP·July 2, 2024

    ARTHRO-LOK BANANA / BEAVER VISITEC

    FDA Adverse Event
    Malfunction ·BEAVER VISITEC·Product code GES·September 16, 2011

    VISITEC

    FDA Adverse Event
    Malfunction ·BEAVER VISITEC·Product code HMX·September 26, 2012

    VISITEC CANNULA ANTERIOR CHAMBER 30 GAGE (10 PER PACK)

    FDA Adverse Event
    Injury ·BEAVER VISITEC WALTHAM MASS·Product code HMX·December 29, 2015

    BVI VISITEC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL·Product code HMX·April 11, 2012

    OPHTHO-BURR 1.0MM

    FDA Adverse Event
    Injury ·BEAVER VISITEC, INTERNATIONAL·Product code HQS·January 12, 2011

    BEAVER MINI-BLADE

    FDA Adverse Event
    BEAVER VISITEC INTERNATIONAL·Product code GES·December 26, 2012

    BEAVER BLADE

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL·Product code GES·June 27, 2011

    GUIBOR CANALICULUS INTUBATION SET

    FDA Adverse Event
    Malfunction ·BEAVER VISITEC INTERNATIONAL·Product code HMX·July 31, 2012

    BVI VISITEC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL·Product code HMX·February 20, 2012