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

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    NEEDLE

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

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867377127·GLENOID INSERTER/IMPACTOR, MEDIUM

    GLENOID INSERTER/IMPACTOR, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·February 9, 2026

    REFLOTRON CREATINE KINASE TEST TABS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DENTAL POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GLENOID INSERTER/IMPACTOR, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·January 10, 2025

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·Product code NBW·December 15, 2009

    MAXIMO II DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·December 14, 2010

    RELION CONFIRM BLOOD GLUCOSE SYSTEM

    FDA Adverse Event
    Malfunction ·ARKRAY, INC.·Product code NBW·January 22, 2013

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014