BEUDAMED
    6 results · 18ms · 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.
    Filters Regulation: Us FDA ×

    VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COMET C-125

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRANSKINETICS INFRARED MULTI-LEAD TELE SYST 7100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 22, 2013

    STEALTHSTATION S7 SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC.·Product code HAW·December 9, 2010

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code LDD·June 20, 2014