BEUDAMED
    13 results · 28ms · Sources: EU EUDAMED, US FDA

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    HOWMEDICA ASYMMETRIC STEM FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704287479·SPURLING-KERRISON PUNCH 8" 4 MILLIMETER FORWARD...

    PISTON SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    R&D PART NOS. 5339, 5510, 5514

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    MEXFLEX TOTAL HIP SYSTEM

    FDA Adverse Event
    Other ·ALPHATEC SPINE, INC.·Product code JDI·August 29, 2006

    GLIDEWIRE GT

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

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL MANUFACTURING CORPORATION·Product code MVK·July 31, 2015

    ISOFLEX S,

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    ACCU-CHEK ® AVIVA EXPERT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·July 24, 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