BEUDAMED
    2,468 results · 25ms · Sources: EU EUDAMED, US FDA

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    L-PHENYLALANINE METHYL ESTER HYDROCHLORIDE PME REA

    FDA 510(k)
    FDA Class 1 ·Hematology

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 7, 2010

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·June 18, 2010

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 6, 2014

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 31, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·September 3, 2015

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 20, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·December 8, 2014

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·March 4, 2010

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 23, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·December 8, 2014

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·January 26, 2007

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·October 6, 2010

    UNKNOWN AXSOS 3 TI PROXIMAL LATERAL HUMERUS PLATE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·December 23, 2019

    UNKNOWN AXSOS 3 TI PROXIMAL LATERAL HUMERUS PLATE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·December 23, 2019

    UNKNOWN AXSOS 3 TI DISTAL MEDIAL TIBIA LOCKING PLATE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·December 23, 2019

    UNKNOWN AXSOS 3 TI DISTAL MEDIAL TIBIA LOCKING PLATE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·December 23, 2019

    UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·December 19, 2012

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·April 28, 2022

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·July 29, 2024