BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    DIODE LASER FOR HIAR REMOVAL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Ambler Value Line

    FDA UDI
    AMBLER SURGICAL CORP.·00190660217563·McGiveney hemorrhoid grasping forceps, 7 1/2'',...

    PROFUSION BONE VOID FILLER KIT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VTS1000

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 4, 2024

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·October 1, 2014

    014 HT WINN GUIDE WIRE

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DQX·May 29, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 16, 2011

    Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG

    FDA Enforcement
    Class II ·Ongoing·ICU Medical Inc.·January 21, 2026