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

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    EarliPoint

    FDA 510(k)
    FDA Class 2 ·Neurology

    SONTEC GELPI RETRACTOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896026483·SONTEC GELPI RETRACTOR MULTIPLE LEVEL OFFSET AR...

    RANDOX SPECIALITY CONTROL (I) LEVELS 1, 2 AND 3

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    FloPatch (FP120)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 21, 2014

    ECHELON 60 ENDOPATH

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 1, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·July 16, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025