BEUDAMED
    18 results · 37ms · Sources: EU EUDAMED, US FDA

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    AP213-01

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD.·Product code FPA·February 7, 2016

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    PAB®

    FDA Adverse Event
    Malfunction ·Product code KPE·July 13, 2021

    AP213-01

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD.·Product code FPA·February 7, 2016

    PROLENE HERNIA SYSTEM MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·April 22, 2025

    MEDPOR Surgical Implant * POREX Surgical Products Group * Sterile/EO * Implant, Non-Pyrogenic, For Single Use Only, CAT #6317 DIM 20mm Diameter * Lot xxxxxx * QTY: 1 * Porex Surgical Inc., 15 Dart Road, Newnan, GA 30265 USA

    FDA Recall
    Terminated ·Porex Surgical, Inc.·Product code HPZ·March 7, 2005

    Avazzia Med-Sport Massager; Model: BEST AV-1; P/N #MS04182-103; manufactured by Avazzia, Inc., Dallas, TX 75240.

    FDA Recall
    Terminated ·Avazzia, Inc·Product code GZJ·June 29, 2007

    MDI Medical Limited

    Importer
    🇮🇪 Ireland·7 Manufacturers

    Abena A/S

    Importer
    🇩🇰 Denmark·20 Manufacturers

    Shanghai International Holding Corp. GmbH(Europe)

    Authorized representative
    🇩🇪 Germany·637 Manufacturers·33064 Devices

    SUNGO Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·1571 Manufacturers·20390 Devices