BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    VPS Rhythm DLX Device with TipTracker Technology

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEXT Medium Strawberry Prophy Paste Box 200

    FDA UDI
    Preventech·D024220363·NEXT Medium Strawberry Prophy Paste Box of 200 ...

    VEO® Lateral Interbody Fusion System

    FDA UDI
    Choice Spine, LP·00840996134187·LATERAL,CURETTE,STRAIGHT RING

    GREAT GLOVE LATEX EXAMINATION POWDERFREE GLOVES WITH PROTEIN LABELLING CLAIMS (50 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SYNGO RT INTERFACE

    FDA 510(k)
    FDA Class 2 ·Radiology

    MICROLET®

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code QRL·April 23, 2026

    MICROLET®

    FDA Adverse Event
    Injury ·ASCENSIA DIABETES CARE US INC.·Product code QRL·April 3, 2025

    ADULT EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BZE·October 31, 2008

    ARCHITECT IPTH

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code CEW·August 23, 2011

    QUADRA ASSURA CRT-D

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·July 11, 2013

    MICROLET®

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code QRL·July 1, 2025

    MICROLET®

    FDA Adverse Event
    Injury ·ASCENSIA DIABETES CARE US INC.·Product code QRL·December 1, 2023