BEUDAMED
    8 results · 41ms · Sources: EU EUDAMED, US FDA

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    EXMOOR AURAL GROMMET AG/TI

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

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970805·

    MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNTHES ZERO-P

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMR CONNECTOR SMALL R

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·September 3, 2020

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·May 15, 2014

    IMPLANTABLE PACING LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·October 31, 2012

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 16, 2010