BEUDAMED
    77 results · 27ms · Sources: EU EUDAMED, US FDA

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    ENDOLED

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

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1671333110·

    WESTCOTT UTILITY SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896099180·WESTCOTT UTILITY SCISSORS BLUNT CURVED ROUND BLADE

    Zavation

    FDA UDI
    Zavation LLC·00197157006143·Sizer with One Stop/0deg/9&10mm

    U BY KOTEX CLICK UNSCENTED MENSTRUL TAMPONS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ALOKA SSD-5000 V5.0 ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 22, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 18, 2015

    PENUMBRA SYSTEM JETD REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·May 8, 2019

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 30, 2015

    PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·June 14, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 26, 2015

    PARADIGM QUICKSERTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code KZH·October 1, 2014

    ASR XL TAP SLV ADAP 12/14+5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 29, 2013

    LIFEPAK 20E DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·May 12, 2011

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 9, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·September 9, 2015

    PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·September 16, 2015

    PENUMBRA SYSTEM 4MAX REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 30, 2015