BEUDAMED
    11 results · 22ms · 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 ×

    Barrx Anorectal RFA Wand

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814534·GENUMEDI SAND SIZE II

    Mouthpiece, Disposable, 1-3/8" O.D., 2.625" L

    FDA UDI
    A-M SYSTEMS, LLC·00817081023831·Mouthpiece, Disposable, 1-3/8" O.D., 2.625" L

    PIPELINE TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTEGRA ELECTRODE TUNNELING NEEDLE

    FDA 510(k)
    FDA Class 2 ·Neurology

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013

    PUMP MMT-522LNAP PRDGM INS PL EN ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·September 8, 2008

    8.5MM MEDULLARY REAMER HEAD

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTO·October 15, 2018

    8.5MM MEDULLARY REAMER HEAD

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code HTO·November 10, 2014

    5.0MM FLEXIBLE SHAFT

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HTO·November 10, 2014