BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    SURGEON'S GLOVE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665584236·MIS Fenestrated Screw, Ø5.0 x 30mm, Ø5.5mm Rod

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110980·STERILIZING CASE PLASTIC LARGE

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869657556·MOSS XT Ti Pedicle Screw Ø5.0x30mm light blue, ...

    Sapphire ULTRA Coronary Dilatation Catheter

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955979279·

    SURESEAL ENDOSCOPIC VALVE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    INTERMEDICS MODEL 366-15 VS 1 HEADER PLUG

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    B1005, ACUCISE ENDOPYELOTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code EYB·April 17, 2017

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014

    REVEAL XT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DSI·December 14, 2010

    ENSEAL TRIO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GEI·December 27, 2012

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 22, 2026

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·February 13, 2025