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

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    MULTIPLE BELTS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO: FMP METAL/METAL ACETABULAR INSERT, MODELS 499-28, 499-34, 499-38

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    Ultrasonic scaler

    FDA 510(k)
    FDA Class 2 ·Dental

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 30, 2014

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·December 20, 2010

    UNKNOWN ZIMMER KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 13, 2013

    AQUACEL AG FOAM

    FDA Adverse Event
    Malfunction ·CONVATEC LTD·Product code FRO·August 18, 2022

    AQUACEL AG FOAM

    FDA Adverse Event
    Malfunction ·CONVATEC LTD·Product code FRO·August 18, 2022

    AQUACEL AG FOAM

    FDA Adverse Event
    Malfunction ·CONVATEC LTD·Product code FRO·August 18, 2022

    BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026