BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    Plato MICROCATH 27B Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO VASCUPUNCTURE PICC GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEXUS TKO-6, LUER-ACTIVATED DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GMK-SPHERE FEMORAL COMPONENT CEMENTED SIZE 4 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 31, 2017

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·June 3, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·September 27, 2014

    UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code LGD·June 29, 2011

    ZOLL IVTM QUATTRO CATHETER

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code NCX·February 26, 2022