BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Coronary Dilatation Balloon Catheter (VesPenetrator®), Coronary Dilatation Balloon Catheter (VesTraveler®), Coronary Dilatation Balloon Catheter (VexPander®)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EarQ

    FDA UDI
    Sbo Hearing A/S·05714464030521·EARQ F30 MINIRITE T C091

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540177445·BIPOLAR FORCEPS

    GELPI SPINAL RETRACTOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896026599·GELPI SPINAL RETRACTOR WITH SPEED LOCK ANGLED TIP

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 12, 2023

    SONIK LDI 20 AIR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OMNI-VUE 2 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 1, 2011

    IAB: 8 FR - 30 CC

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·November 7, 2008

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 16, 2013