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

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    OXYCON-ALPHA

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    POLARCATH PERIPHERAL BALLOON CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Apollo Suture Anchor System and Titan Screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PUMP MMT-715LNAS PRDGM INS V2.1 SK EN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·December 22, 2010

    ESACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·January 4, 2013

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE, 26MM

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·July 17, 2014

    ORTHOPAEDIC SALVAGE SYSTEM NON-MONDULAR TIBIAL PLATE LONG 67

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 29, 2024

    ORTHOPAEDIC SALVAGE SYSTEM TIBIAL POLY BEARING 12MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 29, 2024

    OXF ANAT BRG LT SM SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·May 18, 2021