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

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    SR VIVODENT S, SR ORTHOTYP S, SR ORTHOLINGUAL S

    FDA 510(k)
    FDA Class 2 ·Dental

    ATLAS GOLD PTA DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AURA

    FDA 510(k)
    FDA Class 2 ·Dental

    UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022

    2520274-2013-02868

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·May 29, 2013

    HUDSON CONCHA NEPTUNE

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BTT·September 29, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 17, 2011

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    PEDICLE SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    PEDICLE SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 18, 2023

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 7, 2023

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·November 14, 2023