BEUDAMED
    6 results · 17ms · 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.

    25-HYDROXYVITAMIN D 125I RIA KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    LIFEPAK 50 MONITOR/DEFIBRILLATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APIERON INSIGHT ENO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ASR ACETABULAR IMPLANT 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 28, 2013

    ENDOSCOPIC BILIARY CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code LQR·February 10, 2011

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·July 9, 2014