BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    MEMOMETAL BONE ANCHORS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088

    FDA 510(k)
    FDA Unclassified ·Unknown

    SYNTHES MODULAR FOOT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MULTI-LINK RX VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code MAF·August 5, 2011

    VOYAGER RX CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code LOX·December 14, 2010

    PERCLOSE PROGLIDE¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·September 9, 2025

    PERCLOSE¿ PROSTYLE¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·October 14, 2024

    INFUSOMAT P

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·August 27, 2014

    NONE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 28, 2011

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018