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

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    DX6605E-TENS, DX6605E-G, DX6609-G

    FDA 510(k)
    FDA Class 2 ·Neurology

    CASCADE BATH, MODEL 6900

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BROOKER TIBIA NAILS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 8, 2025

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·June 11, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 9, 2011

    PCA II PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·July 23, 2008

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·July 3, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·May 9, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

    HANDLE CEV102910R DIA 10MM ANG W/RATCHET [MXI/XOM]

    FDA Adverse Event
    Injury ·XOMED MICROFRANCE MFG·Product code GCJ·December 20, 2013