BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    BD PLASTIPAK¿ SYRINGES NON-STERILE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 28, 2023

    GDC 10-3D/3D-SHAPE SYNERG DETECTION CIRCUIT

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORTATION·Product code HCG·February 20, 2007

    GDC 10-STANDARD SYNERG DETECTION CIRCUIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORK LTD.·Product code HCG·November 22, 2006

    GDC 18-SOFT SYNERG DETECTION CIRCUIT

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code HCG·September 13, 2006

    GDC 18 - 3D/3D-SHAPE SYNERG DETECTION CIRCUIT

    FDA Adverse Event
    Malfunction ·NEUROVASCUARL, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code HCG·August 3, 2006

    BD 20 ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 1, 2022

    ACCU-CHEK MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 24, 2011

    GDC SYNERG POWER SUPPLY

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV. OF BOSTON SCIENTIFIC CORP·Product code HCG·September 14, 2006

    MICROCUFF SUBGLOTTIC SUCTIONING ADULT ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code BTR·April 27, 2021