BEUDAMED
    11 results · 32ms · Sources: EU EUDAMED, US FDA

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    iCertainty

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TBA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AVIE A1C TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    BLUNT TIP SCREW, ÿ 4X38MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·August 15, 2024

    BD PRESET¿ ECLIPSE¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 17, 2021

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·June 21, 2013

    CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·July 8, 2011

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 17, 2014

    BLUNT TIP SCREW, ÿ 4X34MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·August 15, 2024

    PROXIMAL HUMERUS, LEFT, LONG, ÿ 8.5X220MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·August 15, 2024

    Fixed Core Wire Guide

    FDA Enforcement
    Class II ·Terminated·Cook Inc.·March 21, 2018