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

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    BELTONE SERIES 100 AUDIOMETERS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    VARIAX

    FDA UDI
    Stryker GmbH·07613327177176·Upper Tray

    N/A

    FDA UDI
    Tyber Medical, LLC·M695M9402160·

    ORTHOPEDIC FIXATION SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CERASORB M ORTHO

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SURFIX STE S. STEEL DIA 3.5 L28MM STERILE

    FDA Adverse Event
    Injury ·NEWDEAL SAS·Product code HRS·June 19, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL, LTD.·Product code KWA·December 23, 2010

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020