BEUDAMED
    31 results · 31ms · Sources: EU EUDAMED, US FDA

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    SURGEON'S GLOVES

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

    Empower Bracket

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746132681·DB BKT SL EMPOWER PASSIVE LL 2ND BIC 018 T-22 A...

    Empower 2®

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746008474·DB BKT SL EMPOWER INTERACT LL 2ND BICUSPID 018...

    Empower Bracket

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746122842·DB BKT SL EMPOWER INTERACT LL 2ND BIC 018 T-22 ...

    Empower 2®

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746011450·DB BKT SL EMPOWER PASSIVE LL 2ND BICUSPID 018 ...

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867050488·LO-PRO SCRW,TI,3.5MMX 22MM

    QUADROX-I SMALL ADULT MICROPOROUS MEMBRANE OXYGENATOR; W/ BIOLINE COATING AND W/ INTEGRATED ARTERIAL FILTER W/ BIOLINE C

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PVS 1300 SYNCHRO 0.014 & PVS 1600 SYNCHRO 0.010 GUIDE WIRES

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·November 8, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·January 2, 2013

    SPACEMAKER PREPERITONEAL DIST BALLOON

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC·Product code GCJ·February 14, 2014

    LO-PRO SCRW,TI,3.5MMX 22MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWC·March 24, 2023

    LO-PRO SCRW,TI,3.5MMX 28MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·September 10, 2018

    LO-PRO SCRW,TI,3.5MMX 18MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·September 10, 2018

    LO-PRO SCRW,TI,3.5MMX 22MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·September 10, 2018

    LO-PRO SCRW,TI,3.5MMX 24MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·September 10, 2018

    PLANTAR LAPIDUS PLATE, STANDARD RIGHT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·September 10, 2018

    KREULOCK SCREW

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRS·August 27, 2024

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·September 5, 2024

    KREULOCK SCREW, TI, 3.5X26

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·September 5, 2024