BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    RE-NEW LAPAROSCOPIC INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471155992·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 230mm

    UreTron PF Series Probe

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

    HLR MODEL 601 HEART LUNG RESUSCITATOR AND HEARTSAVER 100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    E-POLY 36MM +3 MAXROM LNR SZ23

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MAY·January 28, 2022

    PREFACE® GUIDING SHEATH WITH MULTIPURPOSE CURVE

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DYB·February 14, 2013

    PUMP,COLLEAGUE CXE SINGLECHANNEL COLOUR FRENCH LOANER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 17, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 28, 2014