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

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    ARTHROSCOPE ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RENATRON II DIALYZER REPROCESSING SYSTEM RS 8330

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

    VAS-CATH DUALATOR(TM) VESSEL DILATOR

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

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 6, 2010

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 5, 2013

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·July 18, 2014

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023

    JAWS "HIQ+", 5 X 330 MM, SCISSORS, METZENBAUM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 30, 2023

    Robotic Pack, part number AMS4389

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017

    SHAFT "HIQ+", 5 X 330 MM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·May 23, 2023

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023