BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    HI-Q HAND INSTRUMENTS- UROLOGY

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

    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

    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

    LM- LAP 10 HIGH FLOW INSUFFLATOR

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

    HI-LO TEMP THERMOCOUPLE TO THERMISTER ADAPTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRULIANT TIB IMP PS INSERT SZ 5 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·June 2, 2023

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 9, 2013

    MNBR EXT 59IN NDHP

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD·Product code FPK·December 6, 2010

    PENUMBRA COIL 400

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·July 18, 2014