BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    COBE CENTRY 2 BICART OPTION KIT

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

    Sterngold Implant System Guided Latch Driver - PUR.

    FDA UDI
    STERNGOLD DENTAL LLC·00841549118968·Used to turn the implant as it is screwed into ...

    M.D.C. PORTA-LIFT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    OPTIFLUX 180NRE DIALYZER FINISHED ASSY.

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FJI·May 29, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    PRODISC-L INFERIOR PLATE

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·November 18, 2010

    ANATOMIC SHOULDER PROSTHESIS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWS·May 12, 2026