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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    VDW.ROTATE 15.04 6-FILES 25MM

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·January 27, 2023

    VDW.ROTATE 15.04 6-FILES 25MM

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·November 9, 2023

    MONOCRYL (POLIGLECAPRONE 25) SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAN·April 30, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code LWS·October 10, 2012

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 29, 2010

    12MM/130 DEG TI CANN TFNA 420MM/LEFT-STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·September 12, 2019