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.

    OXIMETRIX ACCU SAT CPB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DISC 120 TRANSPORTER

    FDA 510(k)
    FDA Class 1 ·Immunology

    STERRAD (R) 100NX DUO CYCLE TEST PACK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYRINGE 5ML LS 22X1-1/4 AN EMERALD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 18, 2019

    FUNCTIONAL STIMULATION

    FDA Adverse Event
    Malfunction ·NEURO - VILLALBA·Product code LGW·May 15, 2014

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·October 30, 2007

    ATTAIN ABILITY PLUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·October 31, 2012

    BD EMERALD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·August 2, 2019

    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018