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

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    FDA 510(k)
    FDA Class 2 ·Radiology

    RTE SNAPCONE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FHW·July 11, 2023

    BAYER DIAGNOSTICS ADVIA CENTAUR RUBELLA IGM ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    POWDER-FREE NON-VHLORINATED POLYMER COATED LATEX EXAMINATION GLOVES CONTAINS 100 MICROGRAMS OR LESS OF TOTAL WATER EXTRA

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GST GOLD RELOAD, 60MM, 6 ROW

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 6, 2019

    REAR TIP EXTENDER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code N/A·December 30, 2025

    RTE SNAPCONE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FHW·February 17, 2021

    5.5MM TI MIN INVASIVE CURVED ROD 200MM RADIUS/125MM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NKB·March 12, 2013

    PENUMBRA SYSTEM REPERFUSION CATHETER 032

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·May 2, 2013

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·September 15, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 26, 2011