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

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    Solitaire 2 Revascularization Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    ICUFF REPAIR PLATE, RIGHT; CUFF REPAIR PLATE. LEFT; ANCHOR BOLT, 10MM THROUGH 50MM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NCONTACT COAGULATION SYSTEM KIT

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

    GMK-REVISION TIBIAL AUGMENTATION SIZE 4/5MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·October 3, 2019

    BD PRECISIONGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·February 3, 2020

    BD INSYTE AUTOGUARD WINGED

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 3, 2024

    UNKNOWN DEPUY 17.5MM CVD RP TIBIAL KNEE INSERT

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 11, 2013

    IMMULITE 2000

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code DGC·July 14, 2011

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014