BEUDAMED
    14 results · 24ms · 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 ×

    TOXO-SCREEN DA TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    HIGH SPEED EMG MODULE

    FDA 510(k)
    FDA Class 2 ·Neurology

    JBAIDS ANTHRAX DETECTION KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD.·Product code GCX·May 25, 2012

    RECEPTAL 1.5LITER PE/CE WITH (50/CASE)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·August 1, 2011

    NON-PVC RECEPT LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    NON-PVC RECEPT. LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    NON-PVC RECEPT LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    RECEPTAL 1.5 LITER PE/CE WITH (50/CASE)

    FDA Adverse Event
    Injury ·HOSPIRA LTD.·Product code GCX·November 18, 2010

    RECEPTAL 1 LITER/CE WITH VALVE (50/CAS)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·June 24, 2011

    RECEPTAL 1 LITER/CE WITH VALVE (50/CAS)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·June 24, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 27, 2014

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NEK·November 8, 2012

    INOMAX DS (DELIVERY SYSTEM)

    FDA Adverse Event
    Malfunction ·INO THERAPEUTICS, LLC/IKARIA·Product code MRN·September 8, 2010