BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    U-SCOPE 8000 SYSTEM WITH HSC+EMB CANNULA

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

    AGXO

    FDA UDI
    Oticon A/S·05707131258298·H160, RITE 312 WL STG AGXO

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102770·DODICK-KAMMANN CHOPPER STRAIGHT 2.0MM

    ABDOMINAL TOURNIQUET SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MINISPIR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

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

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 29, 2013

    BD NEXIVA CLOSED IV ACCESS SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·August 22, 2008

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code MIH·June 14, 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