BEUDAMED
    4 results · 26ms · 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 FDA Adverse Event ×

    VENTED HIGH VOL. INLET, N/S

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - ENGLEWOOD·Product code LHI·March 20, 2017

    TRI-LOCK BPS SZ 2 HI OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 9, 2014

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 23, 2012

    MAGIC 3 FEMALE INTERMITTENT CATHETER

    FDA Adverse Event
    Malfunction ·ROCHESTER MEDICAL CORP.·Product code KOD·May 27, 2015