BEUDAMED
    79 results · 23ms · Sources: EU EUDAMED, US FDA

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    IVUE 500

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ULTRAFLEX INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEPILEX TRANSFER AG

    FDA 510(k)
    FDA Unclassified ·Unknown

    M.U.S.T. PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·July 20, 2007

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·March 29, 2007

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·July 20, 2007

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·March 29, 2007

    PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

    TOTAL ASR ACET IMP SIZE 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·October 2, 2014

    AEQUALIS

    FDA Adverse Event
    Injury ·TORNIER SAS·Product code KWS·May 23, 2013

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·May 12, 2011

    MECTALIF POSTERIOR

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 2025

    MECTALIF OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12X28X7 L0°

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·November 10, 2017

    MECTALIF (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI 11X22X7 L5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 29, 2020

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 LONG HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 23, 2019

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·May 25, 2023

    SELF-RETAINING SCREWDRIVER FOR LOCKING SCREW

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code FSM·July 9, 2018

    PEDICLE SCREW PEDICLE SCREW 6X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·September 21, 2018

    MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·October 17, 2018