BEUDAMED
    13 results · 26ms · Sources: EU EUDAMED, US FDA

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    Standard Supreme Sterilization Wrapper

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814701·GENUMEDI SILVER SIZE VII

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100837·FLIERINGA FIXATION RING 22MM

    DURAGEN XS DURAL REGENERATION MATRIX

    FDA 510(k)
    FDA Class 2 ·Neurology

    FIBER FORCE

    FDA 510(k)
    FDA Class 2 ·Dental

    CONCEPTUS INC. USA

    FDA Adverse Event
    Injury ·CONCEPTUS INC., USA·Product code HHS·July 18, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2013

    PATIENT ESSENTIALS KIT

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 11, 2008

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 3, 2020

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 2, 2020

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 7, 2020

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 30, 2015

    IPSOGEN JAK2 PCR KIT IVD

    FDA Adverse Event
    QIAGEN GMBH·Product code PSU·September 4, 2018