BEUDAMED
    15 results · 28ms · Sources: EU EUDAMED, US FDA

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    VITAMESH MACROPOROUS PP SURGICAL MESH

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

    Mini-Mono®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70605201·Mini-Mono-Brackets Roth 'N' .018" 1000 Brackets...

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306801808·DeBakey Tissue Forceps, 2.0 mm Tip, 15 cm / 6 in

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482048795·Symmetry® Forceps, Tissue, 1x2 Teeth, 8 in

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345027244·Inserter, 11-16MM, Lumbar Straight

    GEM PREMIER 3000- ADDITION OF GLUCOSE AND LACTATE AS NEW PARAMETERS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    C-IT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 13, 2025

    Widex

    FDA UDI
    Widex A/S·05706069794519·Widex EVOKE E-CIC-M (Light beige ) 220

    Widex

    FDA UDI
    Widex A/S·05706069794526·Widex EVOKE E-CIC-M (Clay brown ) 220

    Widex

    FDA UDI
    Widex A/S·05706069794533·Widex EVOKE E-CIC-M (Dark brown ) 220

    5.0 CM SHORT ATTACHMENT

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·April 10, 2013

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·April 6, 2011

    LIFEPAK 9 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·June 11, 2008

    UNKNOWN BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·March 10, 2017