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

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    INOBLENDER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ArgenZ HT+ 95x12 D2

    FDA UDI
    ARGEN CORPORATION, THE·D818122689·Dental porcelain/ceramic restoration kit

    SAFETYGLIDE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·January 22, 2026

    CONVENTUS ORTHOPAEDICS FRACTURE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO MEDAMICUS AXIA RSN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 22, 2024

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Injury ·ANGIOSCORE, INC·Product code LIT·March 29, 2016

    SPECTRANETICS GLIDELIGHT LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code MFA·May 21, 2013

    RESTORE ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 26, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 14, 2011

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 26, 2015