BEUDAMED
    9 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.

    CEPHALINEX ACTIVATED PTT REAGENT

    FDA 510(k)
    FDA Class 2 ·Hematology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209120222·

    LOGIQ S8

    FDA 510(k)
    FDA Class 2 ·Radiology

    EZ-MIO MANUAL DRIVER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PINNACLE MTL INS NEUT40IDX60OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 20, 2013

    12/14 ARTICUL 40MM M SPEC+12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·August 20, 2013

    TRIDENT POLYETHYLENE RMVL TOOL

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·June 5, 2014

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code GCX·November 12, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 29, 2010