BEUDAMED
    10 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 ×

    my Patch sl

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NorthStar

    FDA UDI
    Seaspine Orthopedics Corporation·10889981231767·W Parallel, Side Loading/Variable

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111451898·TC REES DISS SCISS 6.75 INCHES

    CAPTION APPLICATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VACPLUS SUCTION UNIT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DEPTH ELECTRODE

    FDA Adverse Event
    Malfunction ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·December 14, 2021

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 10, 2014

    PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

    FDA Adverse Event
    MEDEL S.P.A.·Product code BTI·June 11, 2013

    THERMA CARE

    FDA Adverse Event
    Injury ·PFIZER·Product code IMD·July 7, 2011