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

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    ANIMATOR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00843471183724·.022 L/R Std. Weld Size #17

    Threaded K-wire, 25mm threaded, d/e, Ø 4.8mm/229mm

    FDA UDI
    mahe medical gmbh·EMAH00407704170·Threaded K-wire, 25mm threaded, d/e, Ø 4.8m...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659209817·Threaded K-wire, 25mm threaded, d/e, _x000D_...

    ACROSS TRANSSEPTAL ACCESS SYSTEM, 406977, 406978, 406979, 406980, 406981, 406982, 406983, 406984

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Glidewire GT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026

    ONE TOUCH PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·May 13, 2010

    DELTAPLUSH - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·October 3, 2012

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·February 18, 2014

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 21, 2018