BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer

    FDA 510(k)
    FDA Class 2 ·Dental

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    NBX - NON-BRIDGING EXTERNAL FIXATOR - SHOULDER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DISPOSABLE HEMODIALYSIS ACCESS CATHETER SETS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 17, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 11, 2013

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·July 28, 2011

    SFXSPI PDS+ UNI VIO 6IN 3-0 SA SH

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code NEW·October 24, 2024

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    MUST MINI OC PRE-BENT TRANSITION ROD 75° Ø3.5/4X 200MM (STE)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKG·April 25, 2024