BEUDAMED
    11 results · 22ms · 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 Regulation: Us FDA ×

    SUNFLOWER WARNER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ArgenPMMA Multi 98x20-C3

    FDA UDI
    ARGEN CORPORATION, THE·D818120937·Crown And Bridge, Temporary, Resin

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450299180·

    MICROSCAN MICROSTREP PLUS PANEL-AMOXICILLIN/CLAVULANIC ACID

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PC CARE BLOOD GLUCOSE DATA MANAGEMENT SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·December 27, 2012

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 20, 2013

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Malfunction ·OPTONOL, LTD·Product code KYF·July 25, 2014

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FMG·June 13, 2011

    GMK HINGE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·June 2, 2025

    DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·August 10, 2023