BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    OXYGEN BARB M-552

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PFR SLING SYSTEM, PART OF THE AMS PELVIC FLOOR REPAIR SYSTEM

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

    HOSPITALITY SERVER

    FDA 510(k)

    SUPRACONDYLAR NAIL T2 SCN 10 X 200 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS ¿ KIEL·Product code HSB·July 17, 2012

    ATLAS PLUS DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·May 5, 2014

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 15, 2012

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH LTD / HUNTINGTON·Product code HQL·August 4, 2010

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

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