BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    ACA ACETAMINOPHEN ANALYTICAL TEST PACK

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CERASYS - ZR

    FDA 510(k)
    FDA Class 2 ·Dental

    MIDSLEEVE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 21, 2014

    RECAP PF FEMORAL HEAD RESURF 40MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KXA·November 21, 2012

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDI·September 17, 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